To see the other types of publications on this topic, follow the link: Glande salive.
Dissertations / Theses on the topic 'Glande salive'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the top 50 dissertations / theses for your research on the topic 'Glande salive.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Browse dissertations / theses on a wide variety of disciplines and organise your bibliography correctly.
1
RATOMPOSON, RATOMPONIONY GARY. "Tumeurs salivaires a manifestation parapharyngee : a propos de 13 observations cliniques." Aix-Marseille 2, 1990. http://www.theses.fr/1990AIX20128.
Full text
2
RIAD, FOUAD. "Regulation endocrinienne de la secretion salivaire des mineraux chez les bovins." Clermont-Ferrand 2, 1986. http://www.theses.fr/1986CLF21026.
Full text
3
Larsson, Olof. "Peptides as cotransmitters in salivary secretion histochemical, biochemical and functional studies of parotid and submandibular glands /." Stockholm : Kongl. Carolinska Medico Chirurgiska Institutet, 1989. http://catalog.hathitrust.org/api/volumes/oclc/19412146.html.
Full text
4
Yuk-lun, Kam. "The efficacy of a novel lubricating system in the management of radiotherapy related xerostomia." Click to view the E-thesis via HKUTO, 2004. http://sunzi.lib.hku.hk/hkuto/record/B31981835.
Full text
5
Leslie, Martin David. "Salivary gland function after radiotherapy for head and neck cancer." Thesis, University College London (University of London), 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341706.
Full text
6
Eliasson, Lars. "On minor salivary gland secretion /." Göteborg : Department of Cariology, Institute of Odontology, Sahlgrenska Academy at Göteborg University, 2006. http://hdl.handle.net/2077/712.
Full text
7
Sanderson, Christopher Mark. "Transport of IgA in rat salivary glands." Thesis, University of Surrey, 1986. http://epubs.surrey.ac.uk/847984/.
Full textAbstract:
Transport of polymeric immunoglobulin A (plgA) in rat salivary glands has been investigated by combined morphological and biochemical techniques in vivo and in vitro. The distribution of IgA and its cellular receptor secretory component (SC) was observed by immunoperoxidase staining of cryosections from parotid and submaxillary gland, showing serous acinar cells are the site of IgA transport into saliva. Binding of horse radish peroxidase specific IgA to parotid serous acinar cells in vitro, observed by electron microscopy, shows that only the basolateral domain of acinar cells possesses exposed SC. A combination of new cell fractionation methods and standard western blotting techniques shows that SC present on basolateral plasma membrane of parotid acinar cells has a molecular weight (mwt) >100,000 and shows a high affinity for plgA in vitro. The existence of a 73,000 mwt SC occurring with plgA in cellular fractions of parotid gland suggest cleavage of SC occurs prior to secretion. The kinetics of plgA trancytosis was studied using isolated parotid acini. Bound plgA was secreted into the incubation medium as slgA, within thirty minutes of incubation at 37°C. Secretion of plgA was initially rapid but slowed over a 2hr period of incubation at 37°C. In addition to facilitating plgA transport serous acinar cells also synthesise and secrete a diverse range of other salivary proteins which are packaged into secretion granules and secreted directly through the apical plasma membrane. It is improbable that one complex secretory pathway facilitates both bulk secretion of salivary protein and transport of plgA. Therefore secreted proteins must be selectively segregated during secretion into saliva. Secretion of proteins from acinar cells in vitro shows proteins are released at two distinct rates.
8
Laplume, Sylvie. "Analyse biologique de la salive et applications dans les domaines cliniques." Paris 5, 1996. http://www.theses.fr/1996PA05P075.
Full text
9
Mason, Gillian Ivy. "A study of salivary glands and saliva in health and disease." Thesis, University of Birmingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368520.
Full textAbstract:
Much of this thesis describes the use of immunohistochemical methods on salivary glands from patients with Sjogren's syndrome (SS) to quantify the position, nature and proliferative activity of the inflammatory cell infiltrate, deposition of cell matrix proteins and glandular expression of TGFp. Studies are also undertaken on glands from an experimental animal model and from patients with two associated conditions, benign lymphoepithelial lesion (BLEL) and systemic sclerosis (SSc). Initially a rat model of SS was examined and changes in salivary glands quantified at different stages after autoimmunisation. Immunohistochemically there were similarities to SS, in that class II antigen was expressed by glandular epithelium and the early lesions contained T lymphocytes. However, B lymphocytes were rare, the cell infiltrate contained large populations of macrophages and neutrophils, and there was evidence of increased elaboration of fibrous connective tissue. These results indicate that this animal model is of doubtful use for the study of Sjogren's syndrome. Studies on human tissue showed that the lymphocyte infiltrate in BLEL patients was more extensive than SS and that T cells predominated in small foci, whereas B cells were the dominant lymphocyte type in larger foci. In areas of extensive lymphocyte infiltration, B cells were closely associated with ducts or present in germinal centre-like structures with T cells being found elsewhere. A previously unreported feature of BLEL was the presence of intra-epithelial (and intra-lumenal) B cells, many of which were proliferating. The remaining duct walls in BLEL appeared to be under pressure due to this population of B lymphocytes and "holes" were observed both in the basement membrane and at the lumenal surface that may facilitate migration of lymphocytes from glandular stroma into duct lumens. There was significantly more tenascin and fibronectin in BLEL glands (p<0.01) compared to normal parotid controls which contained minimal amounts of these proteins. By contrast, both proteins were expressed in normal labial glands with no significant increase in glands from SS and SSc patients. As both tenascin and fibronectin are important in cell migration, increased levels may be a factor facilitating lymphoid infiltration in BLEL. Absorbance measurements demonstrated that ductal expression of TGFI differed between control, SS and BLEL salivary glands. SS glands showed an increase in expression of all isoforms of TGFß with the increase for TGFP2 and TGFP3 being significant (p=0.02 & p<0.002). By contrast, ductal expression of all isoforms of TGFI in BLEL was reduced in both confluent (p<0.0001) and minimally infiltrated (p<0.005) areas of gland. Thus reduced glandular expression of TGFJ may be important in allowing the high levels of lymphocyte and epithelial cell proliferation detected in BLEL which are rarely seen in SS. Salivary glands from SSc and Raynaud's phenomenon (RP) patients contained small, predominately T cell foci with few proliferating B cells and a significantly increased mast cell population (p<0.005). Fibrosis within the glands was variable and not associated with increased deposition of fibronectin or tenascin. Subjectively, the most obvious difference in TGFI expression in SSc compared to controls was exhibited by fibroblasts. Cell counts revealed no differences in fibroblast expression of TGFßI or TGFß receptors. However, the percentage of TGFß2-positive fibroblasts was significantly higher in SSc glands compared to controls (p<0.004). RP glands showed an intermediate level of expression. By contrast, a lower percentage of RP fibroblasts expressed TGF(33 compared to controls, with SSc glands showing an intermediate level of expression. The results indicate that both SSc and RP are associated with an increased salivary gland mast cell population and changes in expression of TGFß2 and ß3 isoforms by glandular fibroblasts. The final section of this thesis describes an investigation of antioxidant levels in saliva from healthy individuals and patients with SS or periodontal disease. The results demonstrated that in SS there was an increase in the concentration of antioxidants in unstimulated saliva but a reduced rate of production. This diminished output of salivary gland antioxidants may be of significance to the oral health of these patients. In periodontal disease there was a reduction in antioxidant levels in stimulated saliva that may have been the result of local depletion by reactive oxygen species, produced by chronic inflammation within the gingival tissues. Alternatively, these patients may have intrinsically reduced levels of antioxidants and therefore be more susceptible to periodontal disease.
10
Dantas, Aline Maia. "Estudo da relação entre glândulas salivares e doença periodontal em ratos." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/42/42136/tde-09022012-142657/.
Full textAbstract:
A gengivite e a periodontite constituem doenças periodontais infecciosas comuns do homem, nas quais as bactérias periodontais e seus produtos participam ativamente para indução da inflamação local e efeitos sistêmicos (ex.: coração). Sabendo que a saliva representa a primeira e grande barreira às infecções orais, este trabalho se propôs a: i) avaliar a perda óssea induzida pela doença periodontal em ratos submetidos à indução de doença, via implante de ligadura, após os intervalos de 3, 7 e 14 dias; ii) Investigar possíveis alterações de fluxo (estimulado ou não com pilocarpina) e composição salivar nesses animais; iii) avaliar a concentração / expressão de marcadores de estresse oxidativo e inflamatórios em glândulas salivares e em amostras de saliva; iv) avaliar o papel funcional da função das glândulas salivares ex-vivo na produção da amilase. Para isto, ratos Wistar machos (180 -200g) foram submetidos à indução da periodontite através do implante da ligadura, e os parâmetros inflamatórios e bioquímicos foram avaliados nesses animais. Ratos com periodontite no dia 3, quando comparado ao grupo sham, exibiram aumento significativo do fluxo salivar (estimulada com pilocarpina), produção de Ca2+, secreção de proteínas e produção de amilase na saliva, bem como aumento do conteúdo de TBARs em glândulas parótida e da amilase liberada das glândulas submandibulares (GSM). Observou-se, ainda, aumento da expressão de mRNA para iNOS e nNOS em GSM. Em contrapartida, ratos com periodontite após 7 dias exibiram redução da taxa de salivação estimulada (e não estimulada), da produção de proteínas totais e da concentração e secreção de amilase na saliva, muito embora o conteúdo sérico e salivar de TBARs e da atividade de MPO na saliva desses animais mostrou-se elevado em relação ao grupo sham. Não foram observadas diferenças significativas quanto ao conteúdo de TBARs em glândulas salivares, secreção e concentração de Ca2+ na saliva e tampouco sobre o conteúdo de proteínas nitradas em amostras de GSM desses animais. Já no 14° dia visualizou-se um aumento da atividade de NOS Ca2+ dependente e da expressão mRNA das iNOS e nNOS em GSM. Ratos com periodontite, após 14 dias de indução, não exibiram aumento significativo na taxa de salivação, concentração e secreção de Ca2+ salivar, produção e concentração de proteínas totais, amilase na saliva e conteúdo de TBARs em amostras de saliva e glândulas salivares. Ainda, observou-se aumento das atividades da peroxidase/MPO, concentração de nitrato em saliva e proteínas nitradas em GSM e maior concentração de citocinas Th1 / Th2 (IL-4, IL-13 e IL-10) em amostras de GSM. Conclui-se que a indução experimental da doença periodontal em ratos , influencia o funcionamento de glândulas salivares de acordo com os dias de indução, inicialmente estimulando, em um segundo momento inibindo e posteriormente retornando aos níveis basais. Após 7 dias, caracteriza-se como o tempo ideal para a manifestação dos efeitos inibitórios na glândula.Gingivitis and periodontitis are common infectious periodontal diseases in man, in which periodontal bacteria and their products participate actively to induce local inflammation and systemic effects (eg heart). Knowing that saliva represents the first major barrier to oral infections, this study aimed to: i) to assess bone loss due to induced periodontitis in rats, after intervals of 3, 7 and 14 days, ii) to investigate possible changes in flow (or not stimulated with pilocarpine) and salivary composition in these animals, and iii) evaluate the concentration and expression of markers of oxidative stress and inflammation in the salivary glands and saliva samples, and iv) assess the functional role of salivary gland function in ex vivo production of amylase. For this purpose, male Wistar rats (180-200g) underwent induction of periodontitis by implanting the ligature, and biochemical and inflammatory parameters were assessed. Rats with periodontitis on day 3 when compared to sham group, exhibited a significant increase in salivary flow (stimulated with pilocarpine), production of Ca2+, protein secretion and production of amylase in saliva, as well as increased contents of TBARS in the parotid and amylase released from submandibular glands (GSM). There was also increased expression of mRNA for iNOS and nNOS in GSM. In contrast, rats with periodontitis after 7 days exhibited a reduction in stimulated saliva (not stimulated), production and total protein concentration and secretion of salivary amylase, although the content of serum and salivary TBARS and the activity of MPO in saliva of these animals was high compared to the sham group. There were no significant differences in TBARS content in salivary gland secretion and Ca2+ concentration in saliva, nor on the content of nitrated proteins in samples from these animals GSM. By the 14th day envisioned an increase of NOS activity and Ca2+ dependent mRNA expression of iNOS and nNOS in GSM. Rats with periodontitis, 14 days after induction, exhibited a significant increase in the rate of salivation, concentration and salivary secretion of Ca2+, production and concentration of total protein, salivary amylase and content of TBARS in samples of saliva and salivary glands. Still, there was increased activity of peroxidase / MPO, nitrate concentration in saliva and proteins nitrated in GSM and higher concentration of Th1 / Th2 (IL-4, IL-13 and IL-10) in samples of GSM. We conclude that the experimental induction of periodontal disease in rats, influence the functioning of the salivary glands according to the days of induction, initially stimulating, in a second time and subsequently inhibiting return to baseline levels. After 7 days, is characterized as the ideal time for the expression of an inhibitory effect on the gland function.
11
Sardinha, Daniela Abreu. "Xerostomia e hipofunção das glândulas salivares: fisiopatologia e enquadramento clínico." Master's thesis, [s.n.], 2013. http://hdl.handle.net/10284/5250.
Full textAbstract:
Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Medicina DentáriaA saliva desempenha múltiplas funções e tem um papel vital na proteção da saúde dos tecidos moles e duros da cavidade oral. A xerostomia é a sensação subjetiva de boca seca, um sintoma que pode ou não estar acompanhado de hipossalivação, descrita como redução do fluxo salivar estimulado ou não estimulado. Os pacientes com redução do fluxo salivar apresentam maior risco de cáries, infeções fúngicas orais, dificuldades na deglutição e alteração do paladar. As principais causas da hipofunção das glândulas salivares e da xerostomia são doenças sistémicas e os medicamentos. O diagnóstico é baseado em métodos simples, como a medição do fluxo salivar estimulado e não estimulado. Sendo que o tratamento da xerostomia é essencialmente realizado tendo em conta a sua causa e é dividido em quatro categorias: prevenção, tratamento sintomático, estimulação local ou tópica e terapias sistémicas ou estimulação sistémica. Cada categoria será aplicada dependendo da função glandular. Quando há alguma preservação da estrutura da GS os estimulantes salivares (estimulação local ou sistémica) são o mais indicado. Quando as GS encontram-se irreversivelmente danificadas a opção é o tratamento paliativo.
Saliva has multiple functions and plays a vital role in protecting the health of hard and soft tissues of the oral cavity. Xerostomia is the subjective sensation of dry mouth, a symptom that may or may not be accompanied by hyposalivation, described as a reduction of unstimulated and stimulated salivary flow. Patients with reduced salivary flow are at increased risk for caries, oral fungal infections, swallowing problems and altered taste. The principal causes of salivary gland hypofunction and xerostomia are systemic diseases and drugs. The diagnosis is based on simple methods, as measuring both unstimulated and stimulated salivary flow rate. Treatment of xerostomia essentially is carried out in regard to the cause and is divided in four main categories: palliative or symptomatic stimulation, local and systemic stimulation and prevention of complications. Which category will be applied, depending on salivary glands function. In cases when there is still some residual salivary function it was shown that saliva stimulans (local or systemic stimulation) is more appropriate. When salivary glands are irreversible damaged palliative treatment is the best option.
12
Funegård, Ulrika. "Fractionated irradiation of salivary glands : loss and protection of function." Doctoral thesis, Umeå universitet, Kardiologi, 1995. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-100594.
Full textAbstract:
Radiotherapy of malignancies in the head and neck often involves the major and minor salivary glands in the radiation field. Adverse effects, such as dry mouth symptoms, are common after such therapy. The aim of this thesis was to study longitudinal effects of fractionated irradiation to the head and neck on salivary gland function in man and in the rat and to test radioprotection from antioxidant vitamins (retinol, a-tocopherol and ^-carotene). A sharp decrease in parotid saliva flow rate was seen after one week of irradiation in cancer patients, but in some patients recovery was seen two months after completed treatment. Loss and recovery of salivary gland function were dependent on the total dose given. Irradiation with doses of >65 Gy to the parotid glands led to permanent loss of function in the majority of parotid glands, while recovery could be seen after irradiation with doses of <52 Gy. Concentrations of some proteins and electrolytes in saliva were increased during irradiation but no changes remained 18 months after radiotherapy. However, large inter-individual differences were seen. The irradiation effects observed in rats did not greatly differ from those seen in humans, but no recovery of salivary gland function was seen. On the one hand the impairments of saliva flow and composition w ere dose and time dependent, but on the other hand the response pattem differed between salivary components. Morphological alterations were not seen in the rat salivary' glands after tw'O or five weeks but 26 weeks after irradiation. No single model seems to be optimal for studying all parameters. Therefore, to study effects on salivary glands after irradiation the rat model must be adjusted to meet the questions addressed. Supplementation with vitamin A provided no radioprotection, whereas it w'as found that supplementation with a-tocopherol (3.4 mg/day) and ß-carotene (6 mg/day) during irradiation reduced the degree of inflammation and partly preserved salivary gland function. It did not, however, lead to morphometrically detectable differences in proportions of acinar or ductal cells or stroma.Keywords: Irradiation, salivary glands, saliva composition, antioxidantsS. 1-82: sammanfattning, s. 85-152: 6 uppsatser
digitalisering@umu
13
Aksamit, Matthew Stephen. "Bioinformatic analysis of pea aphid salivary gland transcripts." Thesis, Kansas State University, 2014. http://hdl.handle.net/2097/32836.
Full textAbstract:
Master of ScienceBiochemistry and Molecular Biophysics Interdepartmental Program
Gerald Reeck
Pea aphids (Acyrthosiphon pisum) are sap-sucking insects that feed on the phloem sap of some plants of the family Fabaceae (legumes). Aphids feed on host plants by inserting their stylets between plant cells to feed from phloem sap in sieve elements. Their feeding is of major agronomical importance, as aphids cause hundreds of millions of dollars in crop damage worldwide, annually. Salivary gland transcripts from plant-fed and diet-fed pea aphids were studied by RNASeq to analyze their expression. Most transcripts had higher expression in plant-fed pea aphids, likely due to the need for saliva protein in the aphid/plant interaction. Numerous salivary gland transcripts and saliva proteins have been identified in aphids, including a glutathione peroxidase. Glutathione peroxidases are a group of enzymes with the purpose of protecting organisms from oxidative damage. Here, I present a bioinformatic analysis of pea aphid expressed sequence tag libraries that identified four unique glutathione peroxidases in pea aphids. One glutathione peroxidase, ApGPx1 has high expression in the pea aphid salivary gland. Two glutathione peroxidase genes are present in the current annotation of the pea aphid genome. My work indicates that the two genes need to be revised.
14
Kam, Yuk-lun, and 甘玉麟. "The efficacy of a novel lubricating system in the management of radiotherapy related xerostomia." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31981835.
Full text
15
Zenteno, Savin Tania. "Plasma arginine vasotocin and angiotensin II concentrations during saline acclimation in birds with salt glands." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/29892.
Full textAbstract:
Pekin ducks (Anas platyrhynchos), Canada geese (Branta canadensis) and Glaucous-winged gulls (Larus glaucescens) responded differently during acclimation to saline equivalent to full strength sea water. All species were in hydrosmotic balance until they were given 375 mM NaCl. When the birds drank 75 mM NaCl ducks transiently decreased plasma sodium concentration ([Na⁺][formula omitted]) and osmolality (Osm[formula omitted]) and increased cloacal Na⁺ excretion; geese transiently increased hematocrit (Hct), suggesting transient extracellular dehydration; and gulls increased Osm[formula omitted] (but not Hct), suggesting that their Osm[formula omitted] had been below normal when fresh water was offered.
During acclimation to moderately concentrated saline, all species progressively increased plasma arginine vasotocin levels ([AVT][formula omitted]) (without concomitant increase in Osm[formula omitted]) and decreased plasma angiotensin II concentration ([Ang II][formula omitted]) without parallel changes in Hct. Following acclimation to 300 mM NaCl total body water (TBW) was increased in ducks and geese, but acclimation to 375 mM NaCl did not affect TBW in gulls. When they drank 450 mM NaCl, ducks and geese decreased body mass and increased Hct, plasma electrolyte and osmotic concentrations, [AVT][formula omitted] and [Ang II][formula omitted], indicating they were dehydrated. In contrast, saline acclimated gulls did not increase [Ang II][formula omitted] and increased [AVT][formula omitted] less than ducks or geese. Initial [AVT][formula omitted] was not significantly correlated with
sex in either ducks or geese. Female ducks increased [Ang II[formula omitted] and Osm[formula omitted] less than males during exposure to 450 mM NaCl, while female geese increased [Ang II][formula omitted] more than males. Salt gland NaCl secretion and renal water retention counterbalanced NaCl ingested in low to moderately concentrated saline in ducks, geese and gulls, but not in ducks and geese drinking saline equivalent to sea water. Gulls likely maintained simultaneous, concerted function of kidneys and salt glands during high salt intake, while cloacal excretion may have decreased in the Anatidae.
Based on their relative salt secreting efficiencies, plasma ionic concentrations, Osm[formula omitted] and Hct increased much more in ducks than in geese when they drank 450 mM NaCl, and remained unchanged in gulls drinking 375 mM NaCl. Release of AVT and Ang II in birds with salt glands appears to be controlled by a complicated interrelationship between volume and tonicity (threshold for release varies among species), and these (and possibly other) hormones may affect salt gland and kidney function to maintain salt and water balance.Science, Faculty of
Zoology, Department of
Graduate
16
Lepesqueur, Laura Soares Souto. "Efeitos da fibrose cística sobre o microbioma bucal e o proteoma salivar /." São José dos Campos, 2019. http://hdl.handle.net/11449/183394.
Full textAbstract:
Orientador: Cristiane Yume Koga ItoCoorientadora: Marcia Hiromi Tanaka
Banca: Luana Marotta Reis de Vasconcellos
Banca: Bruno Mello de Matos
Banca: Soraya Carvalho da Costa
Banca: Daniel Freitas Alves Pereira
Resumo: A Fibrose Cística (FC) é uma doença genética de elevada prevalência global e que causa função anormal das glândulas exócrinas. As alterações nas funções das glândulas salivares podem impactar a saúde bucal que por sua vez podem influenciar a saúde geral. A boca pode representar um reservatório microbiano de potenciais patógenos e colonizadores das vias aéreas, causando infecções crônicas pulmonares. O objetivo deste estudo foi avaliar os impactos da FC na cavidade bucal, saliva e microbioma bucal. Foram incluídos no estudo 50 pacientes com diagnóstico de FC com idades de 3 a 20 anos, divididos em 2 grupos de acordo com o grau de severidade da doença determinado pelo escore de Shwachman-Kulczycki: G1 (baixa severidade) e G2 (alta severidade). Foi também incluído grupo controle pareado ao grupo de estudo quanto ao gênero e idade (G3, n=50). A presença de lesões de cárie foi avaliada. O impacto da FC sobre a saúde bucal foi avaliado por questionário preenchido pelos pais ou responsáveis. Amostra de saliva estimulada foi coletada de todos os pacientes. O microbioma bucal foi avaliado por Human Oral Microbe Identification using Next Generation Sequencing (HOMINGS) e metodologias de cultivo, para análise da microbiota potencialmente oportunista e cariogênica. Realizou-se ainda a análise proteômica da saliva e quantificação de imunoglobulinas salivares. Os resultados foram analisados e, de acordo com a distribuição dos dados e avaliação desejada, foram aplicados os testes estatístic... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract : Cystic Fibrosis (CF) is a genetic disease with high global prevalence that causes abnormal function of the exocrine glands. The functional alterations of salivary glands and saliva can impact the oral health and influence general health. Oral cavity may represent a microbial reservoir of potential pathogens that can colonize the airways and cause chronic pulmonary infections. The aim of this study is to evaluate the impact of cystic fibrosis on the oral cavity, saliva and oral microbiome. Fifty CF patients aged from 3 to 20 years were divided into two groups according to the disease severity determined by the Shwachman-Kulczycki score: G1 (low severity) and G2 (high severity). Also, age and gender paired control group was included in the study (G3, n = 50). The occurrence of caries was evaluated. The impact of CF on oral health was evaluated by a questionnaire filled by parents or responsible person. Stimulated whole saliva (WS) samples were collected from all patients. The oral microbiome was analyzed by Human Oral Microbe Identification using Next Generation Sequencing (HOMINGS) and by microbiological culture methodologies to evaluate the potential opportunistic and cariogenic microbiota. The proteomic analysis of saliva and quantification of salivary immunoglobulins were carried out. Statistical analysis was performed according to the normality of the data at a significance level of 5%. The applied questionnaire pointed out that oral health did not impact systemic health negatively, according to the parents in all groups. The groups of patients with CF had lower rates of dmft, DMFT, salivary flow rate and initial pH in comparison to the control group. The counts of staphylococcal and yeast from CF groups were significant higher than the controls. All fungal isolates were susceptible to the antifungal agents. Higher incidence of bacterial resistance was ... (Complete abstract click electronic access below)
Doutor
17
Trinca, Vitor. "Análise do padrão de expressão de BhC4-1-GFP em linhagens transgênicas de Drosophila melanogaster." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/17/17136/tde-19072018-104348/.
Full textAbstract:
Nosso laboratório investiga os mecanismos moleculares que promovem o estabelecimento de padrões de expressão gênica regulados no desenvolvimento em eucariotos superiores. Como modelo, utilizamos o gene de pufe de DNA BhC4-1, que é amplificado e expresso de modo regulado na glândula salivar e na glândula protorácica no final do quarto estadio larval de B. hygida. Estudos funcionais em D. melanogaster resultaram na identificação de módulos cis-reguladores (MCRs) na região promotora do gene BhC4-1. O MCR de glândula anelar de 67 bp (-253/-187), promove a expressão de BhC4-1-lacZ na glândula anelar a partir do final do desenvolvimento embrionário. O MCR de glândula salivar de 129 bp (-186/-58), dirige a expressão do transgene nas glândulas salivares de prépupas. A glândula anelar é o principal órgão endócrino larval e em D. melanogaster é o resultado da fusão das glândulas protorácicas (responsáveis pela síntese de hormônios esteroides), corpus allatum (síntese de hormônio juvenil) e corpus cardiacum (glândula neuroendócrina). Neste trabalho foram obtidas 12 linhagens independentes transformadas com uma construção que contém o fragmento (-253/+40) do promotor do gene de pufe de DNA BhC4-1 clonado à montante do gene repórter GFP. O genótipo destas linhagens foi validado utilizando-se Southern blots. Inicialmente as 12 linhagens obtidas foram analisadas quanto ao padrão de expressão de GFP em larvas de terceiro estadio e em prépupas 2 horas. Em conjunto, esta análise revelou que o padrão de expressão de GFP é bastante variável nestas linhagens. A análise do padrão de expressão da proteína repórter foi estendida em duas linhagens representativas da série (- 253/+40)/GFP. Nestas linhagens a expressão de GFP é inicialmente detectada na glândula salivar durante o estágio de prépupa e na glândula anelar a partir do terceiro estadio larval. Diferentemente do anteriormente observado em linhagens (-253/+40)/lacZ, nestas linhagens não detectamos a expressão de GFP em tempos do desenvolvimento anteriores ao terceiro estadio larval. Experimentos de interação gênica revelaram que na ausência do fator de transcrição br, a expressão de GFP é mantida na glândula anelar e abolida na glândula salivar de larvas de terceiro estadio. Os resultados dos experimentos de interação gênica corroboram dados anteriores que indicavam que o conjunto de fatores de transcrição que regulam a expressão de BhC4-1-lacZ na glândula anelar é distinto daquele que promove a expressão do gene na glândula salivar. As linhagens obtidas neste trabalho constituem uma ferramenta a ser utilizada na caracterização de fatores de transcrição tecido-específicos que regulam o gene BhC4-1 na glândula anelar e/ou na glândula salivar a partir do final do desenvolvimento larval.Our laboratory investigates the molecular mechanisms that promote the establishment of developmentally regulated gene expression patterns in metazoans. As a model, we employ the BhC4-1 DNA puff gene, which is amplified and expressed in a regulated manner in the salivary gland and in the prothoracic gland at the end of the fourth larval instar in B. hygida. Functional studies in D. melanogaster resulted in the identification of cis-regulatory modules (CRMs) in the BhC4-1 promoter region. The 67 bp (-253/-187) ring gland CRM drives BhC4-1-lacZ expression in the ring gland from late embryonic development. The 129 bp (-186/-58) CRM salivary gland drives transgene expression in the prepupal salivary glands. The ring gland is the major endocrine organ, and comprises the prothoracic glands (synthesis of ecdysteroid hormones), corpus allatum (synthesis of juvenile hormone) and corpus cardiacum (neuroendocrine gland). In this work, 12 independent lines transformed with a construct containing the BhC4-1 promoter fragment (- 253/+40) cloned upstream of the reporter gene GFP were obtained. The genotype of each line was validated using Southern blots. Initially, the 12 obtained lines were analyzed to investigate the pattern of GFP expression in the third instar larvae and in the 2 hours prepupae. This initial screening revealed that the pattern of GFP expression is highly variable in these lines. The developmental pattern of GFP expression was extended in two representative (- 253/+40)/GFP lines. In these lines, GFP expression is initially detected in the larval and prepupal salivary glands and in ring gland third instar. Differently from previously observed in (-253/+40)/lacZ lines, in these lines we did not detect GFP expression at developmental times prior to the third larval instar. Gene interaction experiments revealed that in the absence of the br transcription factor, GFP expression is maintained in the ring gland and abolished in the salivary gland of third instar larvae. The results of gene interaction experiments corroborate previous data indicating the set of transcription factors that regulate BhC4-1-lacZ expression in the ring gland is distinct from that which promotes gene expression in salivary glands. The lines obtained in this work constitute a tool to characterize the tissue-specific transcription factors that regulate BhC4-1 gene in the ring gland and/or in the salivary gland from the end of the larval development.
18
Abd, El-All M. A. H. "Comparative histological, histochemical, ultrastructural, scanning electron microscopic and functional studies of the integumental glands ...of A. Salina." Thesis, University of Nottingham, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381091.
Full text
19
Leite, Mariana Ferreira. ""Estudo temporal do efeito da administração de tungstato de sódio sobre alguns parâmetros de glândulas salivares e saliva de ratas diabéticas"." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/23/23140/tde-28082006-183554/.
Full textAbstract:
O presente estudo teve por objetivo avaliar a influência da administração do tungstato de sódio (2 mg/ml) num período de 6 semanas sobre alguns parâmetros de parótida, submandibular e saliva de ratas diabéticas induzidas por estreptozotocina. Os grupos estudados foram divididos em controle (C), controle tratado com tungstato de sódio (CT), diabético (D) e diabético tratado (DT). Os parâmetros estudados foram o metabolismo energético, a composição protéica das glândulas e de saliva total estimulada por pilocarpina e isoproterenol, bem como a via de secreção de proteínas. No metabolismo energético foi determinada a concentração de glicogênio e a atividade enzimática da hexoquinase, fosfofrutoquinase-1, piruvato quinase, glicose-6-fosfato desidrogenase, lactato desidrogenase. Foram determinadas a concentração de proteína total, a atividade enzimática da amilase e peroxidase e o teor de ácido siálico em glândulas salivares e saliva. A via de secreção de proteínas foi estudada pela avaliação da expressão de proteína quinase C por western blot. Os resultados obtidos confirmam o potencial hipoglicemiante do tungstato de sódio, bem como sua ação no controle da polifagia, da polidipsia e do peso corporal e glandular. A concentração de glicogênio sofreu um incremento nos grupos diabéticos e o tratamento com tungstato de sódio potencializou esse aumento nas glândulas salivares. A glândula parótida sofreu um aumento de alguns parâmetros da via glicolítica e de sua composição protéica nas semanas iniciais do estudo, com normalização nas semanas finais. O tungstato se mostrou efetivo no controle da atividade de peroxidase em glândulas salivares, com efeitos pouco significativos sobre os demais parâmetros estudados. Os animais diabéticos apresentaram um aumento da proteína total em saliva, porém nenhuma diferença foi observada na atividade da amilase e peroxidase. O tungstato de sódio potencializou o aumento da concentração de proteínas causado pelo diabete além de reduzir a atividade da amilase na saliva dos animais controle e diabético tratados. A glândula submandibular de ratos diabéticos sofreu uma estimulação na expressão de PKC ativa e inativa após uma semana experimental, além de uma alteração do perfil das isoformas da enzima, o tungstato de sódio potencializou esse aumento. Conclusão: O papel do tungstato de sódio no restabelecimento do metabolismo energético não foi observado em parótida e submandibular, mostrando que esse composto não modifica o metabolismo de tecidos periféricos como as glândulas salivares. A ação do tungstato de sódio sobre a atividade da peroxidase em glândulas salivares indica que esse composto pode atuar como auxiliar no sistema antioxidante no organismo. O tungstato de sódio potencializa uma das vias de secreção de saliva pelo estímulo da PKC.The aim of study was evaluate the effect of sodium tungstate administration (2mg/ml) on some parameters of parotid, submandibular and pilocarpine/isoproterenol stimulated saliva of streptozotocin induced-diabetes, during six weeks. The groups were divided in untreated control (C), treated control (CT), untreated diabetic (D) and treated diabetic (DT). The parameters studied were energetic metabolism, proteic composition of glands and saliva, besides the protein secretion pathway. In the energetic metabolism were determinated hexokinase, phosphofructokinase-1, pyruvate kinase, glycose-6-phosphate dehydrogenase and lactate dehydrogenase activities. Were evaluated the total protein concentration, amylase and peroxidase activities and free and total sialic acid content on saliva and salivary glands. The protein secretion pathway was studied by evaluation of expression of protein kinase C by western blot. The results obtained confirm the tungstate potential as hypoglycemic, as well as its action in the polifagia, polidipsia and body and glandular weight control. The glycogen concentration suffered an increment in the diabetic group and the tungstate treatment potentialized the increase in the salivary glands. Parotid glands suffered an increased in some parameters of glycolitic pathway and its protein composition in the initial weeks of study, with normalization in the end of experiment. The tungstate was effective in the control of peroxidase activity in salivary glands, but few effects on the other parameters. Diabetic animals presented an increased of total protein concentration in saliva, but no difference was observed in the amylase and peroxidase activities. Sodium tungstate caused an increased in the total protein concentration and a reduction on amylase activity of saliva in the CT and DT groups. Submandibular gland of diabetic rats suffered stimulation in the active and inactive PKC expression after one week and alteration in the isoforms profile of enzyme. Sodium tungstate potencialized this increased. Conclusion: In this study, was not observed effect of sodium tungstate on energetic metabolism of parotid and submandibular, showing that this compound does not alter the metabolism in the peripheral tissue as salivary glands. The tungstate acts on peroxidase activity, this show the possible action of this compound in the antioxidant system. Sodium tungstate stimulates the protein secretion pathway in the salivary glands.
20
Bizzarro, Bruna. "Efeito da saliva de Aedes aegypti sobre a diferenciação, maturação e função de células dendríticas e na proliferação de linfócitos T." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/42/42135/tde-21092012-082114/.
Full textAbstract:
Mosquitos são os mais importantes vetores de patógenos humanos, transmitindo um amplo espectro de doenças infecciosas emergentes e reemergentes. Nesse cenário, o mosquito Aedes aegypti está entre as espécies mais relevantes. No presente estudo investigamos as atividades do extrato de glândula salivar (EGS) desse mosquito vetor na biologia das células dendríticas e dos linfócitos T. Nossos dados revelam que o EGS não interfere na diferenciação, maturação e função de células dendríticas murinas. Entretanto, componentes salivares desse mosquito possuem um efeito direto sobre linfócitos. O mecanismo de ação do EGS envolveu a apoptose de células T naïve, enquanto células de memória foram mais resistentes a essa atividade. Uma molécula com peso molecular acima de 400 kDa é provavelmente a responsável por esse efeito. Em conjunto, os resultados gerados por esse trabalho contribuem com a elucidação dos efeitos biológicos da saliva de Ae. aegypti na imunidade de seus hospedeiros e, conseqüentemente, seu papel na transmissão de doenças.Mosquitoes are the most important vectors of human pathogens, transmitting a wide range of emerging and re-emerging infectious diseases. In this scenario, Aedes aegypti is a relevant mosquito species. In the present study, we have investigated the activities of the salivary gland extract (SGE) of this mosquito vector on the dendritic cell and T lymphocyte biology. Our data reveals that the SGE does not interfere on the differentiation, maturation and function of murine dendritic cells. However, salivary components of these mosquitoes have a direct effect on lymphocytes. The mechanism of action of SGE involved apoptosis of naïve T cells, while memory cells were more resistant to this activity. A molecule with molecular weight above 400 kDa is likely responsible for this effect. .Taken together, the results generated by this work contribute to the understanding of the biological effects of Ae. aegypti saliva on the host and, consequently, its role on the transmission of diseases.
21
Bhattacharya, Sumit. "Contribution of Purinergic Receptors to Calcium Signaling in Salivary Gland." University of Toledo Health Science Campus / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=mco1353370433.
Full text
22
UEDA, MINORU, TOSHIO SHlGETOMI, TSUNETOSHI HAYASHI, and HIDEAKI KAGAMI. "ASSESSMENT OF THE EFFECTS OF AGING AND MEDICATION ON SALIVARY GLAND FUNCTION IN PATIENTS WITH XEROSTOMIA USING 99mTC-SCINTIGRAPHY." Nagoya University School of Medicine, 1995. http://hdl.handle.net/2237/16091.
Full text
23
Campos, Amândio José Nova. "Estudo clínico em pacientes medicados com inibidores selectivos da recaptação da serotonina e noradrenalida: avaliação da função salivar e repercussão a nível oral." Bachelor's thesis, [s.n], 2008. http://hdl.handle.net/10284/1966.
Full textAbstract:
Monografia apresentada à Universidade Fernando Pessoa para obtenção do grau Licenciado em Medicina DentáriaA saliva desempenha múltiplas funções e tem um papel vital na protecção da saúde dos tecidos moles e duros da cavidade oral. As reduções no fluxo salivar manifestam-se mais frequentemente como sintomas de boca ressequida sendo esta queixa subjectiva denominada xerostomia. Embora a xerostomia seja o indicativo mais frequente de redução da produção salivar, não está invariavelmente associado com hipossalivação. A depressão é a mais comum das doenças mentais estando os antidepressores na primeira linha do tratamento da maioria dos doentes com depressão e a esta classe terapêutica estão, inevitavelmente associados efeitos secundários e reacções adversas sendo a xerostomia um sintoma que parece ser transversal a todos eles. Este estudo epidemiológico, observacional, transversal, analítico tipo caso-controlo, retrospectivo, tem como objectivo avaliar o possível impacto indirecto dos inibidores selectivos da recaptação da serotonina e noradrenalina (ISRS/ISRSN) na integridade dentária e na mucosa oral, tendo em conta o fluxo salivar em repouso e estimulado, relacionado com o tempo de toma, o pH salivar e o diagnóstico de xeroftalmia, tendo sido inspeccionada, detalhadamente, a mucosa oral. A amostra em estudo contou com 60 pacientes os quais foram divididos em dois grupos: 30 medicados com inibidores selectivos da recaptação da serotonina e noradrenalina e os outros 30 não medicados e sem sintomas. Conclui-se que: o tempo de toma de ISRS/ISRSN influencia, de forma inversa, o FSE, isto é, com a duração do tempo de toma, o FSE tende a diminuir e de forma directa, a xeroftalmia, isto é, quanto maior a duração do tempo de toma, maior a sensação subjectiva de boca seca.--- Saliva has multiple functions and plays a vital role in protecting the health of hard and soft tissues in the oral cavity. Reductions in salivary flow manifest themselves more often as symptoms of dry mouth being subjective complaint called xerostomia. Although xerostomia is the most frequent indication of reduced saliva production, is not invariably associated with the licensee hipossalivation. The depression is the most common mental disorders and antidepressants are in the first line of treatment for most patients with depression and this therapeutic class is, inevitably, associated side effects and adverse reactions and xerostomia is a symptom that seems to cross all of them. This study, epidemiological, observational, cross-analytical type case-control, retrospective, aims to assess the possible impact of selective reuptake inhibitors of serotonin and norepinephrine (SSRI/SNSRI) in dentistry and integrity in oral tissues, taking into account salivary flow at rest and stimulated by linking with the time of taking the salivary pH and diagnosis of xerostomia, and was inspected in detail, the oral tissues. The sample under study had 60 patients who were divided into two groups: 30 medicated with selective reuptake inhibitors of serotonin and norepinephrine and the other 30 non-medicated and without symptoms. It was concluded that: the time of taking SSRI/SNSRI influence, in reverse, the ESF, that is, with the length of time that takes, the ESF tends to decline and in a direct manner, xerostomia, that is, as the longer the duration of time that takes, the more subjective sensation of dry mouth.
24
Leinonen, J. (Jukka). "Carbonic anhydrase isoenzyme VI: distribution, catalytic properties and biological significance." Doctoral thesis, University of Oulu, 2008. http://urn.fi/urn:isbn:9789514289903.
Full textAbstract:
Abstract
Secretory carbonic anhydrase isoenzyme VI (CA VI) catalyses the reversible hydration of carbon dioxide (CO2 + H2O ↔ HCO3- + H+). Low concentrations of salivary CA VI are associated with high decayed, missing or filled teeth (DMFT) index scores and a high incidence of acid injury in the upper gastrointestinal tract plus lowered taste and smell perception. Two mechanisms of action for CA VI have been proposed: acid neutralisation and growth factor function.
In the present study the distribution and catalytic properties of CA VI have been examined in order to further clarify its mechanisms of action and biological significance. CA VI was found to be present and secreted by the alveolar epithelium of the mammary gland, serous acinar cells of lingual von Ebner’s glands, serous demilune cells of posterior lingual mucous glands and serous cells of submucosal tracheobronchial glands. CA VI was also found in the serous cells in the tracheobronchial mucosal epithelium, taste pore, taste bud, base of the tracheobronchial cilia, bronchiolar Clara cells and enamel pellicle. An immunofluorometric assay showed that the mean concentration of CA VI in colostral milk was eight times higher than that in mature milk (35 mg/l vs. 4.5 mg/l). Stopped-flow spectroscopy measurements revealed that the dehydration activity of CA VI is moderate (maximum kcat = 3.0 × 105 · s-1).
The finding that CA VI is a potent catalyst of acid neutralisation emphasizes the possible role of the pellicle bound CA VI in local neutralisation of the acidic metabolic products of dental biofilm. The function of CA VI in von Ebner’s glands’ saliva is likely taste stimuli modification via CA activity although other functions may exist. Its role in milk or respiratory tract mucus remains open, however, as these secretions do not have significant acid predispositions that would need enzymatic catalysis for removal.
25
Jurysta, Cédric. "Etude du flux salivaire de glucose et des transporteurs de l'hexose exprimés dans les parotides de sujets sains et diabétiques." Doctoral thesis, Universite Libre de Bruxelles, 2016. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/228910.
Full textAbstract:
Previous epidemiological studies have shown that the diabetic population has a poor oral status compared to healthy subjects. While changes of the local microcirculation observed during diabetes can somehow explain periodontal pathologies this hypothesis does not stand for the carious decay. We propose the hypothesis that the increase of carious incidence might be linked to changes in the salivary composition, such as an increase of salivary glucose concentrations.The amount of glucose in saliva has been widely discussed in various scientific articles. Subsequently, we performed an initial study that allowed us to confirm that the concentration and excretion of glucose in the saliva were higher in diabetic patients compared to normal patients. In diabetic patients, the relative increase in salivary glucose concentration is even comparable to the rise of blood glucose.We conducted experimental studies in animals in order to investigate the presence and the level of expression of glucose transporters (GLUT1, GLUT2, GLUT4, SGLT1) in rat parotid glands. Through immunohistochemical labeling techniques, gene expression studies and protein expression studies, we demonstrated that GLUT1, GLUT4 and SGLT1 were found in rat parotid glands of normal and diabetic rats. Functional studies targeting the activity and the flux through those glucose transporters strengthened our hypothesis on the potential role of glucose transporter in salivary glucose.This original work introduce for the first time the hypothesis of a secretion mechanism of glucose by the salivary glands through GLUT1 & SGLT1 transporters, the first one being located on the apical and baso-lateral membranes of acinar cells, while the second one is located on the baso-lateral membrane. Secretion of glucose by the parotid gland is no longer at any doubt even though further studies must now specify the specific mechanisms.Doctorat en Sciences dentaires
info:eu-repo/semantics/nonPublished
26
Carvalho, Polliane Morais de 1981. "Evaluation of masticatory, salivary and anthropometric function, presence of volatile sulphur compounds in young adults and changes in salivary gland pos adipogenesis induction in animal model = Avaliação da função mastigatória, salivar, antropométrica, presença de compostos sulfurados voláteis em adultos jovens e alterações em glândula salivar após indução de adipogênese em modelo animal." [s.n.], 2014. http://repositorio.unicamp.br/jspui/handle/REPOSIP/287939.
Full textAbstract:
Orientador: Maria Beatriz Duarte GaviãoTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba
Made available in DSpace on 2018-08-26T13:36:25Z (GMT). No. of bitstreams: 1 Carvalho_PollianeMoraisde_D.pdf: 2230005 bytes, checksum: a03e416e657adde52ad89b778975278c (MD5) Previous issue date: 2014
Resumo: Este estudo investigou a função mastigatória, o paladar, a presença de compostos sulfurados voláteis (CSV) e a bioquímica salivar em sujeitos saudáveis (18-33 anos), e a indução de adipócitos em glândula salivar e suas implicações em modelo animal. Três estudos foram conduzidos, apresentados na forma de capítulos. Capítulo 1: Investigou a performance e habilidade mastigatória, paladar e a possível relação com gênero, índice de massa corporal (IMC), circunferência de cintura (CC) e fluxo salivar estimulado (Stim) e não estimulado (Unst). Foram avaliados 171 indivíduos, (125? 46?). A performance mastigatória foi determinada pela capacidade de fragmentação do Optocal plus e habilidade mastigatória com o uso da escala visual analógica (EVA). O paladar foi verificado pela percepção dos quatro sabores primários. A estatística descritiva, teste de normalidade, correlação, comparação e modelos de regressão foram utilizados, sendo as variáveis dependentes a função mastigatória e o paladar e as independentes: gênero, idade, variáveis antropométricas e fluxo salivar. Na análise de regressão linear múltipla, as variáveis independentes não predisseram o modelo para performance mastigatória. Com a habilidade mastigatória (HM) o modelo explicou 14% da variabilidade e para o paladar 5%. Os resultados indicaram que a performance não foi relacionada com parâmetros antropométricos e salivares em indivíduos jovens saudáveis. A habilidade foi relacionada com IMC, CC e gênero. O paladar foi fracamente relacionado ao IMC e CC. Capítulo 2: Verificou a bioquímica salivar e presença de CSV e a possível interferência do IMC, fluxo e pH stim/unst. Para a verificação dos CSV foram avaliados 71 voluntários (57? 14 ?), utilizando o aparelho Oral chromeTM. Foram determinadas as concentrações de proteína total, cálcio, fosfato, amilase e ureia em 171 voluntários (125? 46 ?), em saliva stim/unst. A bioquímica salivar foi semelhante em relação à antropometria. No entanto, as respectivas concentrações diferiram significativamente entre saliva Stim/Unst, com exceção da amilase. Os indivíduos apresentaram quantidades semelhantes de CSV em relação ao IMC. Em indivíduos com valores críticos de metilmercaptana (CH3SH) observou-se correlação significativa (r=0.51) com o pH (unst). Capítulo 3: Investigou o eventual aparecimento de adipócitos nas glândulas salivares em modelo animal (camundongos). A adipogênese foi realizada com dieta rica em gordura, e ainda via receptor de proliferadores de peroxissoma gamma (PPAR gama) com rosiglitazona. Western blot, histoquímica e imunoistoquímica foram utilizadas. Análise de microarray foi realizada para verificar o efeito da dieta. Anticorpos: fosfo-4E BP1 e tirosina hidroxilase marcaram a atividade de mTOR e nervos, respectivamente. O microarray mostrou um número significativo de alterações genéticas. Em relação à dieta observou-se baixa ou nenhuma expressão de fosfo 4E-BP1 e aumento na atividade de tirosina hidroxilase. Em camundongos tratados com rosiglitazona verificou-se ativação de mTOR e tirosina hidroxilase. Conclusão: Pelos resultados dos três capítulos concluiu-se que em indivíduos jovens e saudáveis a função mastigatória e paladar não foram influenciados pelo padrão salivar e foram fracamente relacionados ao antropométrico. A bioquímica salivar e presença de CSV foi semelhante em relação à antropometria. Observaram-se mudanças relacionadas à atividade do sistema nervoso em glândula salivar de camundongos devido à dieta rica em gordura ou ativação de PPAR gamma
Abstract: This study investigated masticatory function, the presence of volatile sulfur compounds (VSC) and salivary biochemistry in healthy subjects (18-33 years), and also the induction of adipocytes in the salivary gland and its implication in an animal model. Three studies were conducted, presented as chapters. Chapter 1: Investigated the performance and chewing ability, taste, and the possible relationship to gender, body mass index (BMI), waist circumference (WC) and stimulated salivary flow (Stim) and unstimulated (Unst). 171 individuals (125? 46?) were evaluated. Masticatory performance was determined by the ability of fragmentation Optocal plus and chewing ability with the use of visual analogue scale (VAS). Taste was verified by the perception of the four primary flavors. Descriptive statistics, normality tests, correlation, comparison and multiple linear regression models were used. In multiple linear regression performance was not predict by the independent variables in the model. With chewing ability the model explained 14% of variability and 5% for the taste. The results indicated that masticatory performance was not related to anthropometric parameters and saliva in healthy young subjects. The ability was related to BMI, WC and Gender. Taste was weakly related to BMI and WC. Chapter 2: Verify the salivary biochemistry and presence of VSC and the possible influence of BMI, flow and pH (Stim)/(Unst). For the verification of VSC 71 volunteers (14 57? ?) were assessed using the Oral chromeTM device. The concentrations of: total protein, calcium, phosphate, urea and amylase were investigated in 171 volunteers (46 125? ?) in saliva (Stim) / (Unst). Biochemical salivary were similar in respect of anthropometry. However, the concentrations differed significantly between saliva (Stim)/(Unst), with the exception of amylase. The sample presented similar amounts of CSV in relation to BMI. In individuals with critical values of methylmercaptan (CH3SH) we observed a significant correlation (r = 0:51) with pH Unst. The results indicate that in healthy young subjects salivary biochemistry and VSC exhibit similar behaviour in relation to BMI. The (CH3SH) when greater than the normal limit concentration was correlated to pH Unst. Chapter 3: We investigated the possible appearance of adipocytes in the salivary glands in animal model (mice). Adipogenesis was performed with high-fat diet, and also via peroxisome proliferator-gamma (PPAR gamma) with rosiglitazone . Western blot, histochemistry and immunohistochemistry were used. Microarray analysis was performed to assess the effect of diet. Antibodies: phospho-4E-BP1 and tyrosine hydroxylase marked mTOR and nerves activity, respectively. The microarray showed a large number of genetic changes. Regarding diet was observed low or no expression of phospho-4E-BP1 and an increase in tyrosine hydroxylase activity. In mice treated with rosiglitazone there was activation of mTOR and tyrosine hydroxylase. The results suggest that there are changes in salivary gland innervation before stimuli for adipogenesis. Conclusion: We concluded that in healthy young individuals masticatory function was not influenced by the salivary pattern and was weakly related to anthropometric. Salivary Biochemical and presence of CSV was similar in relation to anthropometry. There are alterations in the activity of the nervous system in the salivary glands of mice due high fat diet or activation of PPAR gamma
Doutorado
Anatomia
Doutora em Biologia Buco-Dental
27
Paula, Fernanda de. "Mapeamento dos canais de água no processo de morfogênese das glândulas salivares humanas: estudo topográfico das aquaporinas 1,3 e 5." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/5/5133/tde-10082016-125353/.
Full textAbstract:
Introdução: As glândulas salivares humanas passam por diversos e complexos processos durante o período de desenvolvimento, até que adquiram maturidade estrutural para desempenhar sua função, a formação e secreção de saliva. Considerada essencial à saúde e homeostase da cavidade oral, a saliva é um fluido aquoso que depende de um mecanismo de transporte entre as membranas celulares por meio das aquaporinas. A família de proteínas aquaporinas possui treze membros. Somente algumas dessas proteínas atuam nas glândulas salivares formando poros na bicamada lipídica das membranas celulares facilitando o transporte de água e pequenos solutos, cruciais à regulação da qualidade e quantidade de saliva secretada. Proposição: Diante deste cenário, avaliamos por meio da técnica de imunoistoquímica o padrão de expressão das aquaporinas 1, 3 e 5 de glândulas salivares em desenvolvimento, com o intuito de contribuir com informações de base para futuras pesquisas. Metodologia: 47 espécimes parafinados de glândulas salivares em desenvolvimento, de diferentes sítios da cavidade oral de 20 fetos humanos, com idade entre 14 e 25 semanas, foram submetidos à técnica de imunoperoxidase. Os resultados foram analisados, de acordo com o estágio da morfogênese glandular e localização da expressão das aquaporinas. Resultados: Na fase de botão, houve a expressão das aquaporinas 1, 3 e 5 em todas as células epiteliais; na fase pseudoglandular, a expressão dessas proteínas foi vista nos ductos rudimentares (com exceção da aquaporina 1) e nas porções terminais (futuros ácinos); na fase canalicular as aquaporinas foram principalmente detectadas nos ácinos rudimentares e ductos. Finalmente, na fase de botão terminal, as aquaporinas 3 e 5 foram detectadas nas membranas das células acinares e os ductos expressaram todas as aquaporinas. Conclusão: O presente trabalho evidenciou a imunoexpressão das aquaporinas 1, 3 e 5 nas glândulas salivares humanas durante o período de embriogênese. A análise topográfica dessas proteínas nos permitiu identificar diferenças no padrão de expressão entre as diferentes regiões estruturais e estágios do desenvolvimento glandular, sugerindo diferentes papéis para cada proteínaIntroduction: The human salivary glands morphogenesis depends on complex processes during the development period until they reach full structural maturity to perform its function - the synthesis and secretion of saliva. The saliva is a complex aqueous fluid considered essential to health and homeostasis of the oral cavity; its synthesis depends on several molecular mechanisms, including the transport of water, solutes, ions, amongst others across the cell membranes. The aquaporin family of proteins is essential in this process. This protein family consists of thirteen members that form channels across the cell membrane facilitating water and small solutes transportation, crucial to the regulation of quality and quantity of secreted saliva. Aims: In this scenario, we evaluated, using the immunohistochemistry technique, the expression pattern of aquaporins 1, 3 and 5 in the different phases of salivary glands development, in order to understand the role of these protein in the formation of human salivary gland morphogenesis. Methodology: 47 specimens of paraffin embedded human salivary glands at various developmental phases were included in the study. The specimens were derived from various sites of the oral cavity of 20 human fetuses aged between 14 and 25 weeks of gestation. All specimens were subjected to the imunohistochemical immunoperoxidase technique. The results were qualitatively and semiquantitatively analyzed according to the stage of glandular morphogenesis and express location of aquaporin. Results: In the bud stage, there was expression of aquaporin 1, 3 and 5 in all glandular epithelial cells; in pseudoglandular stage, the expression of these proteins was seen in rudimentary ducts (except aquaporin-1) and the terminal end buds (future acini); in the canalicular phase the aquaporins were mainly detected in the rudimentary ducts and acini. Finally, in terminal bud stage, the aquaporin 3 and 5 were detected in the membranes of the ducts and acinar cells expressed all aquaporins. Conclusion: This study showed the presence of aquaporins 1, 3 and 5 in human salivary glands during embryogenesis period. The topographic analysis of these proteins allowed us to identify differences in the expression pattern between the different structural regions and stages of glandular development, suggesting different roles for each of these proteins
28
Gonçalves, Liliana Maria do Vale Costa. "Avaliação do pH salivar em pacientes submetidos a radioterapia à região de cabeça e pescoço." Master's thesis, [s.n.], 2015. http://hdl.handle.net/10284/5245.
Full textAbstract:
Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Medicina DentáriaA disfunção das glândulas salivares, como sequela da Radioterapia (RT) traduz-se geralmente em hipofunção salivar e consequente diminuição do pH. Este estudo avaliou o comportamento do pH salivar num grupo de 35 indivíduos submetidos a RT com fracionamento convencional, por tumores malignos da região de cabeça e pescoço. O acompanhamento foi obtido através de três avaliações a cada indivíduo. A primeira avaliação foi realizada antes do tratamento, a segunda após 15 sessões de tratamento e a última depois de terminado o tratamento. O pH salivar foi determinado através de indicadores de alaranjado de metilo e azul de bromotimol, colocados na face dorsal da língua. A média do valor de pH registada antes do tratamento foi 6,69. A medição intermédia demonstrou diminuição do valor de pH da saliva para 6.37, baixando para 6,31 até ao final do tratamento (p>0,05). Estes resultados demonstraram que a RT, no tratamento de tumores da cabeça e do pescoço, parece reduzir o pH salivar, sendo este valor dose-dependente.
The dysfunction of the salivary glands, as an effect of radiotherapy (RT), usually generates a salivary hypofunction and subsequent decrease of the pH value. This study aimed to evaluate the salivary pH behaviour in a group of 35 individuals under RT with conventional fractionation, for malignant tumours of the head and neck regions. The follow-up was obtained through three assessments to each individual. The first evaluation was conducted before treatment, the second one after 15 treatment sessions and the last one at the end of the treatment. The salivary pH was determined by methyl orange indicator and bromothymol blue indicator placed on the dorsal surface of the tongue. The average pH recorded before the treatment was 6.69. The intermediate measurement showed a diminution of the saliva pH value to 6:37, dropping to 6.31 by the end of treatment (p> 0.05). These results revealed that the RT for the treatment of tumours of the head and neck regions appears to reduce the salivary pH value, which is dose-dependent.
29
Junior, Walter Luiz Siqueira. ""Estudo de alguns parâmetros salivares em indivíduos com síndrome de DOWN"." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/23/23140/tde-13062005-115943/.
Full textAbstract:
O objetivo deste estudo foi mensurar o fluxo salivar, pH, capacidade tampão, concentrações de proteína total e ácido siálico, atividades das enzimas amilase e peroxidase e concentração dos íons sódio, potássio, cálcio, fósforo, zinco e magnésio em saliva total de indivíduos síndrome de Down com idade entre 1 e 25 anos. Nos indivíduos com idade entre 1 e 5 anos a saliva total foi coletada através de uma leve sucção, enquanto que nos outros indivíduos com idade entre 6 e 10, 11 e 15, 15 e 20, 21 e 25 a saliva total foi coletada com estimulação mecânica através da mastigação de parafilm, durante 10 minutos. O pH e a capacidade tampão foramdeterminadas usando um pHmetro digital. A capacidade tampão foi mensurada através de titulação com HCl a 0,01N. A concentração de eletrólitos foi determinada através de um espectrofotômetro de emissão atômica com fonte de excitação de argônio induzido. A proteína total foi mensurada através do reagente de Folin. A atividade da amilase foi mensurada através da produção de maltose e a atividade da peroxidase foi mensurada através da utilização de orto-dianisidina. Para a analise estatística os dados foram apresentados em media ± desvio padrão. Foi utilizado o teste t de Student para determinar as diferenças entre as medias dos indivíduos síndrome de Down e o grupo controle. Nenhuma diferença significante foi observada na concentração de ácido siálico, fósforo, zinco, magnésio e cálcio entre os indivíduos síndrome de Down e o grupo controle. A concentração de sódio, proteína total e a capacidade tampão demonstraram ser maior nos indivíduos com síndrome de Down em comparação ao grupo controle. Por outro lado, o fluxo salivar, a concentração de potássio, e a atividade das enzimas amilase e peroxidase foram menores no grupo síndrome de Down quando comparado ao grupo controle. Estes resultados sugerem que as pessoas com síndrome de Down apresentam alterações no metabolismo do ducto e/ou das células acinares das glândulas salivares.The aim of this study was to measure the flow rate, pH, buffer capacity, sialic acid, total protein concentrations, amylase and peroxidase activities and sodium, potassium, calcium, phosphorus, zinc and magnesium concentration whole saliva of individuals with Down syndrome aged 1 - 25 years. In individuals aged 1-5 years the whole saliva was collected under slight suction, while in the others individuals aged 6-10, 11-15, 15-20, 21-25 the whole saliva was collected with stimulation by chewing a piece of parafilm, for 10 minutes. The pH and the buffer capacity were determined using a digital pHmeter. The buffer capacity was measured by titration with 0.01 N HCl. Electrolyte concentrations were determined by inductively coupled argon plasma with atomic emission spectrometry. Sialic acid was determined by thiobarbituric acid assay. Protein was determined by the folins phenol reagent. Amylase was assayed measuring the maltose produced by the breakdown of starch and peroxidase with ortho dianisidine. For statistical analysis the date are presented as mean ± SD. Students t test was used to determine differences between the mean of the Down syndrome and control groups. No statistically significant differences were observed in sialic acid, phosphorus, zinc, magnesium and calcium concentration between the individuals with Down syndrome and control group. The sodium and total protein concentration and buffer capacity showed higher in the Down syndrome than in the control group. On the other hand the flow rate and potassium concentration, amylase and peroxidase activities were lower in the Down syndrome than in the control group. These results suggest that the Down syndrome persons present alteration in the metabolism of the duct and/or acinar cells of salivary glands.
30
Nogueira, Fernando Neves. ""Sistema antioxidante e peroxidação lipídica em glândulas salivares de ratos diabético"." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/23/23140/tde-17112004-181932/.
Full textAbstract:
O objetivo do presente estudo é o de verificar o efeito do diabetes na atividade de constituintes do sistema antioxidante das glândulas salivares submandibular (SM) e parótida (P) de ratos. Para indução do diabetes foi injetado em ratos, via intraperitonial, estreptozotocina (60mg/kg de peso corporal) dissolvido em tampão citrato de sódio 0,1M pH 4,5. Quarenta e oito horas após sua indução foi determinada a glicemia no sangue dos animais. Somente aqueles ratos que apresentaram glicemia superior a 350mg de glicose/100 ml de sangue foram considerados diabéticos. Após o período experimental, os animais foram sacrificados, sendo removidas as glândulas salivares e sangue para análise. Foram determinadas, através de espectrofotometria, as atividades das enzimas superóxido dismutase (SOD), catalase (CAT) e glutationa peroxidase (GPx). O conteúdo de glutationa reduzida (GSH) e oxidada (GSSG) foi determinado em HPLC. A peroxidação lipídica foi determinada no sangue e nas glândulas salivares SM e P usando o ácido tiobarbitúrico (TBARS), que reage com o malonaldeído (MDA) decorrente da peroxidação lipídica. Os resultados mostram um aumento na concentração de malonaldeído no sangue e na glândula submandibular, mas não na glândula parótida. A concentração de GSH e GSSG é maior na glândula SM em relação ao grupo controle, enquanto que a concentração de GSH é menor na glândula P. Não há diferença na atividade da enzima SOD em nenhuma das glândulas salivares. As enzimas CAT e GPx tem a sua atividade específica aumentada somente na glândula parótida. Na glândula submandibular, nenhuma destas duas enzimas sofrem alterações nas suas atividades. Podemos concluir que o sistema antioxidante das glândulas salivares respondem de forma diferente 30 dias após a indução do diabetes. Na glândula SM não há alteração na atividade das enzimas estudadas, porém há um aumento na peroxidação lipídica. Na glândula P, há um aumento na atividade das enzimas CAT e GPx, não sendo encontrado aumento da peroxidação lipídica.The aim of the present study is to determine the effect of diabetes in the activity of some contents from the antioxidant system of submandibular (SM) and parotid (P) salivary glands. The diabetic state was induced by an injection of streptozotocin (60mg/kg body weight) dissolved in 0,1M sodium citrate buffer pH 4,5. Forty-eight hours after the injection, blood was collected and the glycemia determined. Only those animals presenting a blood glucose above 350mg glucose/100ml blood was used in the study. Thirty days after the induction of the diabetes, the animals were sacrificed, the salivary glands were removed and blood was collected and used in the determinations. The activity of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) was determined in spectrofotometer. The content of reduced (GSH) and oxidized (GSSG) glutathione was determined in HPLC. The lipid peroxidation was determined in blood and in SM and P glands, measuring the tiobarbituric acid (TBARS) which reacts with malonaldeyde (MDA) from lipid peroxidation. The results show an increase in MDA concentration from SM and blood, but not on P gland. The content of GSH and GSSG from SM gland increase, and the content of GSH from P gland decreased. There is no difference in the activity of SOD in both salivary glands. The activity of CAT and GPx from P gland increase, but in SM gland there is no difference. We can conclude that the antioxidant system from the salivary glands have different responses in diabetes state after 30 days of the induction. In SM gland, there is no difference in the activity of the enzymes, but we have an increase in the MDA content. In P gland, we have an increase in the CAT and GPx activity, but not in MDA concentration.
31
Dsamou, Micheline. "Protéome salivaire et sensibilité à l'amertume chez l'Homme." Phd thesis, Université de Bourgogne, 2012. http://tel.archives-ouvertes.fr/tel-00935220.
Full textAbstract:
L'amertume fait partie intégrante de notre alimentation. Elle est par exemple fortement représentée dans certaines boissons (ex: café) ou dans certains légumes tels les crucifères. Néanmoins, la perception de l'amertume varie entre les individus et certains aliments considérés comme bénéfiques pour la santé peuvent être rejetés en raison de leur goût amer. Des facteurs génétiques (ex : polymorphisme génétique des récepteurs du goût amer) ou environnementaux (ex : âge, prise de médicaments) expliquent en partie les variations interindividuelles dans la perception de l'amertume. Cependant, d'autres facteurs péri-récepteurs pourraient intervenir, notamment la composition salivaire. Afin d'investiguer dans un premier temps le lien existant entre le protéome salivaire propre à un individu et sa sensibilité à l'amertume, le seuil de détection du goût amer de la caféine a été mesuré sur 29 hommes sains. Leur salive au repos a été étudiée par électrophorèse mono- et bidimensionnelle. L'analyse par électrophorèse bidimensionnelle de la salive au repos des 6 sujets les plus sensibles et 6 les sujets les moins sensibles à la caféine a permis la détection de 255 spots, dont 26 étaient significativement différents entre hyper- et hyposensibles. L'identification de ces 26 spots a révélé la surexpression de fragments d'alpha amylase, de fragments d'albumine sérique, et de sous-unités alpha de l'immunoglobuline A ainsi que la sous-expression de cystatine SN chez les hypersensibles. Ce dernier résultat a été confirmé par Western Blot. Ceci a permis de formuler une hypothèse sur le rôle de la protéolyse en bouche sur la sensibilité à l'amertume. Dans un deuxième temps et afin d'étudier l'effet des molécules amères sur la composition salivaire, une étude in vitro a été menée sur la lignée cellulaire de glandes salivaires humaines HSG différenciées en acini ou non. Après une mise au point des conditions de différenciation (culture dite en 3D), la cystatine SN a été détectée dans les cellules HSG par Western blot après traitement des cellules à la caféine, à la quinine, et à l'urée. Après traitement à la caféine à 5, 50 ou 100µM, une quantification par ELISA a mis en évidence que la cystatine SN était toujours plus abondante dans les cellules HSG différenciées que dans les cellules non-différenciées. Spécifiquement dans les cellules différenciées, l'exposition à la caféine induisait une sur-expression de cystatine SN, la teneur maximale en cystatine SN étant observée avec la caféine à 50 µM. La présence de cystatine SN a également été détectée dans les milieux de culture
32
Ibuki, Flávia Kazue. "Estudo do efeito da irradiação com laser de baixa intensidade no sistema antioxidante de glândulas salivares de ratas diabéticas induzidas por estreptozotocina." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/23/23140/tde-09112010-111500/.
Full textAbstract:
O objetivo do presente estudo foi o de analisar o efeito da irradiação com laser em baixa intensidade no sistema antioxidante enzimático de glândulas salivares submandibular (GSM) e parótida (GP) de ratas diabéticas induzidas por estreptozotocina. As ratas foram inicialmente divididas em grupos não-diabéticas (C) e diabéticas (D) e mantidas pelo período experimental de 30 dias. No vigésimo nono dia as ratas foram subdivididas em seis grupos, sendo três grupos de animais não diabéticos (C0, C5 e C20) e três de animais diabéticos (D0, D5 e D20), de acordo com a dose de irradiação laser que cada grupo recebeu (0, 5 e 20 J/cm2 respectivamente). Para a indução do diabetes foi realizada a injeção intraperitoneal de estreptozotocina (60 mg/kg de peso corporal) dissolvida em tampão citrato de sódio 0,1 M, pH 4,5. Os animais pertencentes aos grupos C (não diabéticos) receberam a injeção somente do veículo. As glicemias foram verificadas 72 horas após a indução do diabetes, para a confirmação do estado diabético nos grupos D. Foram considerados diabéticos os animais que apresentaram glicemia superior a 250mg de glicose/dl de sangue. A irradiação com laser em baixa intensidade seguiu a metodologia determinada pelo método de Simões et. al. (2009). Os animais foram eutanasiados 24 horas após a irradiação, sendo imediatamente removidas as glândulas salivares para a realização das análises bioquímicas. Foram determinados através de espectrofotometria, os valores de total antioxidante (TAS) e as atividades das enzimas superóxido dismutase (SOD), catalase (CAT) e glutationa peroxidase (GPx). Através da análise dos resultados podemos concluir que em GSM de ratas diabéticas o laser com dose de 20J/cm2 causou aumento na atividade da enzima SOD. E independente da dose, causou aumento nos valores de TAS e atividade da enzima CAT. Já em GSM de ratas não diabéticas a dose de 20J/cm2 causou diminuição dos valores de TAS. E independente da dose a irradiação com laser levou a um aumento da atividade da enzima CAT. Nas parótidas de ratas diabéticas, independente da dose, a irradiação com laser causou diminuição da atividade da enzima CAT. E em GP de ratas não diabéticas a dose de 5J/cm2 causou diminuição da atividade da enzima CAT.The aim of the present study was to analize the effect of low-power laser irradiation in the antioxidant enzymatic system of submandibular (GSM) and parotid (GP) salivary glands of diabetic rats induced by streptozotocin. The rats were initially divided into non-diabetic animals (C) and diabetic-animals (D) and maintained by the experimental period of thirty days. Twenty-nine days after diabetes induction, the animals were randomly divided into six groups: three diabetic groups (D0, D5 and D20) and three non-diabetic groups (C0, C5 and C20), according with laser irradiation dose that each one received (0, 5 and 20J/cm2, respectively). For diabetes induction an intraperitoneal injection of streptozotocin (STZ) (60mg/Kg body weight), dissolved in 0.1M sodium citrate buffer, pH 4.5 was performed. In non-diabetic animals, only the citrate buffer was used. The diabetes condition was confirmed seventy-two hours after animals have received the STZ injection. Rats with blood glucose level higher than 14mM (250 mg/100ml) were considered diabetic. The laser irradiation was performed according to Simões et.al. method (2009). Twenty-four hours after the irradiation rats were euthanized. Then, immediately after the euthanasia, salivary glands were removed for biochemical analysis. The total antioxidant values (TAS) and the activity of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxide (GPx) enzymes were determined in spectrophotometer. Analyzing the results we can conclude that in GSM of diabetic rats the laser irradiation with 20J/cm2 increased the SOD activity. With the two different doses, increased the TAS values and CAT activity. However, in GSM of non-diabetic rats, laser irradiation with 20J/cm2, decreased the TAS values and led to an increase in CAT activity, regardless of the dose. In parotid glands laser irradiation decreased the CAT activity with either dose of 5J/cm2 or 20 J/cm2 and the laser irradiation with dose of 5J/cm2, decreased the CAT activity in parotid glands of non-diabetic rats.
33
Lascane, Nelise Alexandre da Silva. "Avaliação do status das glândulas salivares parótida e submandibular na displasia ectodérmica hipoidrótica por meio da ultrassonografia." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/23/23141/tde-18082010-121333/.
Full textAbstract:
Displasia ectodérmica hipoidrótica é uma doença genética rara, clinicamente caracterizada por alterações envolvendo os dentes, pele e suas estruturas anexas. Manifestações orais comuns incluem anadontia ou oligodontia, dentes conóides e xerostomia. Poucos relatos associam displasia ectodérmica e redução do fluxo salivar. O objetivo desse estudo é analisar possíveis alterações nas glândulas salivares de dez portadores de displasia ectodérmica que fazem acompanhamento no Departamento de Dermatologia Pediátrica da Universidade de São Paulo. Ultrassonografia foi realizada em dez casos em infantes portadores de displasia ectodérmica hipoidrótica nas suas glândulas salivares parótida e submandibular. Três apresentaram alterações na glândula parótida e/ou submandibular. Aplasia ou hipoplasia das glândulas salivares maiores é associada a casos de displasia ectodérmica e sugere-se acompanhamento rotineiro das glândulas salivares maiores usando ultrassonografia para prevenção de alterações decorrentes da hiposalivação na cavidade oral.Background- Hypohidrotic ectodermal dysplasia is a rare genetic disease, clinically characterized by defects involving skin and their adnexal structures, as well as oral structures such as teeth, and occasionally salivary glands. These latter manifestations include anodontia or hypodontia, conical teeth and xerostomia. Objective- To analyze possible alterations in major salivary glands of ten patients with ectodermal dysplasia, using image exam. Methods- Ultrasonography was performed in ten pediatric cases of hypohidrotic ectodermal dysplasia to investigate the status of parotid and submandibular salivary gland. Results- Three patients presented aplasia/hypoplasia of at least one gland examined. The other 7 patients did not present any alterations in parotid and submandibular glands. Limitations- Although ultrasonography exam is adequate to investigate the presence and status of major salivary glands, other important glands such as sublingual and minor mucous salivary glands are not well-visualized using this technique. Conclusions- Aplasia or hypoplasia of the major salivary gland is strongly related to ectodermal dysplasia and we suggest routine evaluation of the major salivary gland using ultrasound to monitor and manage the possible impact of xerostomia in oral health.
34
Costa, Thiago Roncini Gomes da. "A família IRM de moléculas de adesão celular durante a histólise da glândula salivar larval de Drosophila melanogaster." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/17/17136/tde-26042018-162637/.
Full textAbstract:
RESUMO: O complexo Irre Recognition Module (IRM) é um importante subgrupo de proteínas transmembranares da superfamília das imunoglobulinas que desempenham função de adesão celular e participam de diversos processos do desenvolvimento de Drosophila melanogaster, tais como: direcionamento axonal, fusão de mioblastos, espaçamento dos órgãos sensoriais, autofagia das glândulas salivares, eliminação de células suplementares e especificação de destino celular na retina pupal. A família IRM é composta por quatro membros bem caracterizados: roughest (rst; irregular-chiasmC); kin-of-irre (kirre); hibris (hbs) e sticksand-stones (sns). Uma característica marcante entre dois membros deste grupo, kirre e rst, é a ocorrência de redundância funcional durante o processo de fusão de mioblastos na musculatura somática embrionária e na fase de \"cell sorting\" das células interomatidiais na etapa final de padronização da retina pupal de Drosophila. Neste contexto, foi observado que kirre pode suprir a ausência ou diminuição nos níveis de expressão de mRNA de rst para manter o fenótipo selvagem destes tecidos. Em glândulas salivares larvais de Drosophila, modelo amplamente utilizado para estudo da morte celular programada (MCP), mutantes rstD, um alelo semidominante de rst, apresentaram fenótipo de persistência deste tecido mesmo após 12 horas à sua eliminação observada em animais selvagens. Considerando o importante processo de redundância funcional promovido por membros do grupo IRM, durante o desenvolvimento de tecidos de Drosophila melanogaster, avaliamos a correlação entre os 4 membros deste grupo durante o processo de autofagia da glândula salivar larval. Para tanto, os níveis de transcrição de genes do complexo foram analisados por RT-qPCR após a formação do pupário até o desfecho do processo de histólise. Verificamos uma diminuição a nível transcricional de rst após o pico no título de ecdisona que leva a histólise da glândula em animais selvagens, e níveis alterados dos mRNAs dos membros do complexo em animais mutantes rstD. Contudo, a superexpressão de rst não foi suficiente para gerar glândulas persistentes. Além disso, descrevemos a localização espacial, por imunohistoquímica, dos membros do complexo, enfatizando a colocalização de rst e kirre, contrariamente aos membros sns e hbs.ABSTRACT: The complex Irre Recognition Module (IRM) is an important subgroup of transmembrane proteins of the immunoglobulin superfamily that play a role in cell adhesion and participates in several processes of development of Drosophila melanogaster, such as: axonal targeting, fusion of myoblasts, spacing of sensory organs , autophagy of the salivary glands, elimination of supplementary cells and specification of cellular target in the pupal retina. The IRM family is composed of four well-characterized members: roughest (rst; irregular-chiasmC); kin-of-irre (kirre); hibris (hbs) and sticks-and-stones (sns). A striking feature of this group is the occurrence of functional redundancy during the process of fusion of myoblasts in the embryonic somatic musculature and in the phase of cell sorting of the interomatid cells in the final step of standardization of the pupal retina of Drosophila. In this context, it can be concluded that it can not provide an absence or decrease the mRNA expression levels of maintaining the wild tissue phenotype. In larval salivary glands of Drosophila, a widely used model for the study of programmed cell death (MCP), rstD mutants, a semidominant rst allele, showed persistence phenotype of this tissue after 12 hours for its observed elimination in wild animals. During the development of Drosophila melanogaster tissues, we evaluated a correlation between the 4 members of this group during the autophagy process of the salivary gland. To that end, transcription levels of complex genes were analyzed by RT-qPCR after patient formation until the end of the histolysis process. We have seen a transcriptional decrease in the first unpronounced postdoc peak of ecdysone leading to histolysis of the gland in wild animals, and altered levels of mRNAs of the complex members in rstD mutant animals. However, a first overexpression was not enough to generate persistent glands. In addition, we describe a spatial location, by immunohistochemistry, of two members of the complex, emphasizing a first and second hand colocalization, unlike the sns and hbs members.
35
Francesquini, Fernanda de Camargo. "Avaliação da especificidade do efeito da saliva do flebotomíneo vetor sobre a infectividade da espécie de Leishmania: infecção experimental de Leishmania (L.) amazonensis e Leishmania (V.) braziliensis com a saliva de Lutzomya flaviscutellata e Lutzomyia (Psychodopygus) complexus em camundongo BALB/c." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-20052014-104624/.
Full textAbstract:
No ciclo natural de transmissão da leishmaniose, as fêmeas infectadas de flebotomíneos regurgitam promastigotas na pele de hospedeiro junto com a saliva. Tem sido descrito que componentes da saliva do vetor possuem propriedades imunomodulatórias que facilitam o estabelecimento da infecção no hospedeiro, contudo a maior parte dos estudos emprega lisado de glândula salivar (LGS) de vetores colonizados em laboratório. Dessa forma, o principal objetivo deste estudo foi avaliar a especificidade do LSG dos flebotomíneos Lutzomyia flaviscutellata e Lutzomyia (Psychodopygus) complexus capturados no campo na infectividade de Leishmania (Leishmania) amazonensis e Leishmania (Viannia) braziliensis. Camundongos BALB/c foram inoculados no coxim plantar traseiro com formas promastigotas de L. (L.) amazonensis e L. (V.) braziliensis na ausência ou presença do LGS de L. flaviscutelata, e L. (P.) complexus. A evolução da infecção foi acompanhada semanalmente e biópsias do ponto de inoculação foram coletadas para análise histopatológica e determinação de carga parasitária na 4ª e 8ª semana pós-infecção (PI); e o linfonodo de drenagem para caracterização de subpopulações de linfócitos T por citometria de fluxo. Células de linfonodo de drenagem foram também cultivadas, com estímulo homólogo, para quantificação de citocinas (IL-10, IL- 12 e IL-4) no sobrenadante. A infecção por L. (L.) amazonensis e L. (V.) braziliensis não se mostrou exacerbada nos grupos co-inoculados com o LGS de ambas as espécies em relação ao grupo controle, inoculado somente com o parasito. O tamanho de lesão e carga parasitária do grupo controle foi maior ou igual aos grupos com saliva. Na infecção por L. (L.) amazonensis houve diminuição dos linfócitos CD4+ e aumento na população de linfócitos CD8+ enquanto na infecção por L. (V.) braziliensis houve manutenção da população de linfócitos CD4+ e aumento de linfócitos CD8+ em todos os grupos quando comparados ao grupo saudável. A produção de IL-10 e IL-12, não diferiram entre os grupos, assim como a produção de IL-4 no grupo infectado por L. (V.) braziliensis. No entanto, nos grupos infectados apenas com L. (L.) amazonensis e com saliva de L. flaviscutellata, foi observada uma maior produção de IL-4 em relação ao grupo saudável. De forma geral, os resultados mostraram que a saliva de L. flaviscutellata e de Lutzomyia (P.) complexus, no seu binômio natural vetor/parasito ou não, não favoreceram o estabelecimento da infecção causada por L. (L.) amazonensis e L. (V.) braziliensis em camundongos BALB/c.During the natural transmission of leishmaniasis, the infected female phlebotomine regurgitates promastigotes into the host\'s skin together with the saliva. It has been reported that components of vector saliva contain immunomodulatory properties that facilitate the establishment of infection in the host, however the most studies employed salivary gland lysate (SGL) of laboratory colonized vectors. Thus, the main objective of this study was to evaluate the specificity of SGL of the phlebotomines Lutzomyia flaviscutellata and Lutzomyia (Psychodopygus) complexus caught in the field in the infectivity of L. (L.) amazonensis and L. (V.) braziliensis. BALB/c mice were inoculated in the hind footpad with promastigotes of L. (L.) amazonensis and L. (V.) braziliensis in the absence or presence of L. flaviscutelata, and L. (P.) complexus SGL. The evolution of the lesion size was evaluated weekly and biopsies from the site of infection were collected for histopathological analysis and determination of parasite load in the 4th and 8th week post infection (PI), and the draining lymph node to characterize subsets of T cells by flow cytometry. The draining lymph nodes cells were also cultured with specific antigen to determine the cytokines (IL-10, IL-12 and IL-4) in the supernatant. L. (L.) amazonensis and L. (V.) braziliensis infection was not exacerbated in the groups co-inoculated with the SGL of both species in the control group, only inoculated with the parasite. The lesion size and parasite burden of the control group was higher or equal to the groups with saliva. In L. (L.) amazonensis infection there was a decrease of CD4+ cells and an increase in the population of CD8+ cells while in L. (V.) braziliensis infection there was a maintenance of CD4+ cells and an increase in the population of CD8+ cells in all groups compared with the health group. The production of IL-10 and IL-12, did not differ between groups, as well as the production of IL-4 in the group infected by L. (V.) braziliensis. However, in the groups infected only with L. (L.) amazonensis in the presence of L. flaviscutellata saliva, it was observed a higher production of IL-4 in relation with the health group. As a whole, the results show that the saliva of L. flaviscutellata and L. (P.) complexus, in the natural vector/parasite binomium or not, did not favor the establishment of the infection caused by L. (L.) amazonensis and L. (V.) braziliensis in BALB/c mice
36
Leirião-Riva, Fernanda Pereira. "Anatomia dos tecidos moles e glândulas salivares do sistema estomatognático de cães e gatos: enfoque anátomo-cirúrgico." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/10/10132/tde-21062006-183449/.
Full textAbstract:
Sabendo que o conhecimento do sistema estomatognático é de fundamental importância para que os clínicos e cirurgiões cheguem a um diagnóstico preciso e instituam o tratamento adequado, propôs-se o presente estudo, que consistiu na dissecção da cabeça de quatro cadáveres caninos e quatro felinos. O objetivo foi a descrição e documentação das estruturas musculares e tegumentares detalhando a origem e inserção, inervação e função de cada estrutura dos tecidos moles bem como a descrição completa das glândulas salivares para a aplicação clínico-cirúrgica na prática odontológica de cães e gatos.Concerned about the knowledge of the stomatognatic system as of fundamental importance to the practitioner and surgeons to reach a precise diagnosis and institute the appropriate treatment, the present study was proposed, consisting in the dissection of the head of four canine and four feline cadavers. The objective was the description and doccumentation of the muscular structures and tegument, detailing the origin and insertion, inervation and function of each structure of the soft tissue as well as the complete description of the salivary glands for a clinical-surgical application in dentistry.
37
Reuterving, Carl-Olof. "Salivary glands and oral lesions in diabetes mellitus : an experimental and clinical study with special reference to the influence of metabolic control and duration of the disease." Doctoral thesis, Umeå universitet, Medicin, 1987. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-100544.
Full textAbstract:
Diabetes mellitus is associated with several clinically significant abnormalities in the oral cavity and salivary glands, the most common being periodontitis, salivary gland enlargement and a sensation of dry mouth. The prevalence of dental caries in diabetics is mostly reported to be decreased or unaffected. Since there is a shortage of information concerning the influence of metabolic control and duration of diabetes on these abnormalities, the present studies were performed. Three-month-old rats were made alloxan-diabetic and investigated after one and twelve months’ duration of diabetes for oral lesions and feeding behavior. They had free access to a standard pellet diet and tap water. Streptococcus mutans and lactobacilli were naturally occurring. In diabetic rats the proportion of the oral flora which was lactobacilli was positively correlated to the blood glucose level. Untreated long-term alloxan-diabetic rats developed advanced periodontal disease and root surface caries in the molars at sites of interdental impaction of foreign material. The degree of alveolar bone loss was positively correlated to the blood glucose level. Diabetic rats were hyperphagic and had a longer total eating time, including day-time eating, mainly by having longer meals but no significant increase of meal frequency, as compared with non-diabetic animals. The untreated alloxan-diabetic rats developed reduced salivary gland weight which was of the same degree in short- and longterm diabetic animals. Short- and long-term untreated alloxan-diabetic rats showed a similar degree of morpho- metrically estimated lipid accumulation in the acinar cells of the submandibular glands, and the degree was positively correlated to the blood glucose level. However, lipid inclusion occurred only in rats with a morning nonfasting blood glucose level exceeding 15 mmol/L. The capillaries in the submandibular glands of the untreated long-term alloxan-diabetic rats had a significantly increased thickness of the basement membranes as compared with the observations in short-term diabetic and non-diabetic rats. Untreated alloxan-diabetic rats were also shown to have a decreased salivary flow rate compared with non-diabetic rats, and the decreased flow was negatively correlated to the blood glucose concentration. Salivary flow rate increased with the duration of the disease. The diabetic rats had increased salivary glucose levels, which were positively correlated to blood glucose values when the latter were above 15 mmol/L, suggesting a threshold mechanism for salivary glucose excretion. Insulin therapy reversed salivary flow rate and salivary glucose concentrations toward normal. Salivary investigations were performed in eleven diabetic patients on two occasions with different metabolic control. Salivary flow rate showed marked interindividual differences but was not significantly changed by improved metabolic control although several of the patients initially had severely deranged glucose metabolism. A positive correlation between the glucose concentration in blood and saliva was seen in the parotid saliva during secretory stimulation. No significant change in electrolytes, amylase or antimicrobial factors was found.S. 1-48: sammanfattning, s. 49-90: 5 uppsatser
digitalisering@umu
38
Cavenaghi, Fabiano Misael. "Efeitos de inibidor de protease sobre os epitélios de revestimento e glandular do rato." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/58/58137/tde-19032010-110726/.
Full textAbstract:
O tratamento anti-HIV conhecido como HAART (Highly Active Antiretroviral Therapy) se tornou comum por volta de 1996, e utiliza 3 ou 4 diferentes medicamentos em combinação - geralmente dois inibidores de transcriptase reversa + 1 ou 2 inibidores de protease. A introdução desse tipo de tratamento trouxe um grande impacto na morbidade e mortalidade de indivíduos infectados pelo HIV. Os inibidores de protease (PIs) são uma boa alternativa às falhas terapêuticas observadas com o uso dos inibidores de transcriptase reversa, no entanto também são associados a vários efeitos tóxicos, como desconforto abdominal, vômito, diarréia, dor de cabeça, tontura, lipodistrofia, hipercolesterolemia, hipertrigliceridemia e hiperglicemia. Em função da existência de efeitos adversos e da condição do ritonavir como protótipo desse tipo de medicação, nosso objetivo é avaliar o efeito desse medicamento sobre os epitélios de revestimento e glandular relacionados à cavidade bucal, de forma a identificar a possibilidade da existência de complicações bucais relacionadas ao uso de inibidores de protease. Ratos albinos (Wistar) foram tratados com Ritonavir (10mg/Kg) por períodos de 4 e 8 semanas. Foram avaliadas as taxas séricas de triglicérides e colesterol (total, HDL, LDL, VLDL). Ao final dos períodos de tratamentos propostos, os animais foram sacrificados, e as peças utilizadas no estudo foram colhidas, (sangue, pele, língua, palatos e glândulas salivares). O sangue coletado foi imediatamente centrifugado sendo o plasma foi utilizado para avaliação das lipoproteínas. Os tecidos colhidos foram fixados, descalcificados quando necessário, processados para inclusão em parafina, cortados com 6µm de espessura, montados em slides e corados com hematoxilina e eosina, para avaliação histopatológica, morfométrica e estereológica. Os dados colhidos foram apresentados em valores médios, e as diferenças analisadas por testes estatísticos adequados para a comparação entre as amostras. Nossos resultados mostram pequenas variações nas características morfológicas de epitélios de revestimento e glandulares, variações essas que poderiam deixar esses tecidos mais propensos a sofrer alterações significativas com traumas ou injúrias, comuns nos tecidos bucais. Embora observadas com pequeno grau de expressão, essas variações, parecem ser progressivas, ou seja, mais expressivas com o uso continuado do medicamento. Mais estudos devem ser realizados, principalmente voltados para avaliações histoquímicas, bioquímicas e moleculares, no entanto nosso estudo é um alerta inicial para a avaliação dos tecidos bucais de pacientes que utilizam inibidores de protease.HAART had a dramatic impact on the HIV infection, however, protease inhibitor exhibit significant drug-drug interactions, and side effects. There are only few data on effects of protease inhibitors on oral tissues. We propose to observe experimental effects of ritonavir on oral epithelial tissues, covering and glandular. Wistar rats received Ritonavir twice a week for 4-8 weeks. Controls received no treatment. At the time for sacrifice, plasma were collected for evaluation of triglycerides, total cholesterol, HDL, LDL and VLDL. Were also collected skin, tongue, palate and glandular tissues Lipoproteins were evaluated and histological examination of skin, mucosal epithelium on tongue, palate and salivar submandibular glandula were made under light microscope. Morphometric methods (cariometry and stereology) were used. Data were statistically analysed by Kruskal Wallis test for multiple samples, since our data were considered not-normal. P[U] 0.05 were considered statistically significant. Our results show that protease inhibitor may be associated with small alterations in epithelial tissues, significant mostly when on longer times using the medication. The complete significance of this data has to be better understood, and other studies has to be done to define these points.
39
Galeano, Zioneth Judith Garcia. "Mudanças morfológicas e glandulares associadas ao polietismo etário em Polybia paulista (Hymenoptera: Vespidae)." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/59/59131/tde-23042010-163030/.
Full textAbstract:
A divisão de trabalho é um dos temas centrais no estudo dos insetos sociais. Nas abelhas e nas vespas essa atividade é regulada pelo polietismo etário. Vários autores mostraram que o polietismo etário de Apis mellifera tem ativação seletiva das glândulas com o trabalho feito dentro da colônia, além de diminuição do peso corporal ao começar o forrageio. Nos vespídeos sociais, o polietismo etário é um tema pouco explorado. Com o objetivo de identificar e descrever em Polybia paulista estas mudanças corporais e glandulares relacionadas à idade dos indivíduos ou com o seu uso na função social, analisaram-se operárias de diferentes idades mantidas em cativeiro desde a sua emergência nas quais foi restrita a interação social desde sua emergência e operárias de diferentes idades coletadas desde o ninho onde a interação social foi completa. Operárias de Polybia paulista mantidas em cativeiro aumentaram a massa corporal, diminuíram a massa do mesosoma e diminuíram a secreção das glândulas salivares e mandibular conforme de acordo com o aumento da idade. Isso difere daquelas operárias que foram permitidas do desenvolvimento social normal (grupo controle), onde foi observado um aumento na massa corporal, na massa do mesosoma e na secreção das glândulas salivar e a mandibular em relação ao aumento da idade das vespas. Provavelmente, o relacionamento social estimula a formação e a transição fisiológica relacionada ao polietismo etário em Polybia paulista. Nestas vespas, mudanças corporais e glandulares observadas foram relacionadas com idade, sendo provável que a interação social e o uso das estruturas nas diferentes tarefas dentro da colônia estejam influenciando tais mudanças. Como conseqüência, fatores que atuam sobre a demografia da colônia, como a fase de desenvolvimento ou o bem-estar da colônia, podem ser determinantes na regulação do polietismo etário. Estes resultados contrastam com o modelo proposto para o polietismo etário da abelha Apis mellifera e com observações da atividade glandular na vespa social Polistes versicolorThe division of labor is a central theme in the study of social insects. In bees and wasps this ability is regulated for age castes of the workers. In Apis mellifera, several authors have shown selective activation of the glands for job in colony, and reduced body weight for foraging. In social wasps age polyethism among workers is a relatively unexplored subject. We tried to identify and to describe in Polybia paulista if the bodily and glandular changes are related to the age of the wasps or to the use of the structures in the social function. Workers of different ages at which was restricted social behavior since its emergence and workers of different ages with full social development were analyzed. When Polybia paulista was in captivity, increased body mass, decreased the mass of mesosoma and decreased the salivary and mandibular glands secretion in relation to the age advancement of the wasps. While, allowing normal social development, there was an increase in body mass, the mass of the mesosoma and the salivary and mandibular glands secretion in relation to age. Apparently, social interaction activates the formation and transition of age castes in Polybia paulista. In these wasps the bodily and glandular changes observed were related to age. Probably social interaction and the use of structures within the nest are influencing the direction of such changes. As consequence, factors that influence the demography of the colony, as the development stage or the welfare of the colony, may be decisive in the age castes regulation. These results contrast with the model proposed for the Apis mellifera age polyethism and with observations of glandular activity in the social wasp Polistes versicolor.
40
Florezi, Giovanna Piacenza. "Xerostomia na doença do enxerto contra o hospedeiro: análise das alterações glandulares e dos níveis salivares das citocinas envolvidas nas respostas Imunológicas Th17." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/23/23139/tde-27112017-131058/.
Full textAbstract:
A doença do enxerto contra o hospedeiro (DECH) é uma das maiores causas de mortalidade e morbidade pós-transplante de células-tronco hematopoiéticas. A DECH, em sua manifestação crônica (DECHc), ainda não tem sua fisiopatologia totalmente esclarecida; entretanto, o envolvimento do sistema imunológico, por meio de respostas imunes inatas e adaptativas é bem estabelecido na literatura. A DECHc afeta múltiplos órgãos, incluindo as glândulas salivares, o que tem, como causa imediata, a xerostomia. Essas alterações são largamente desconhecidas e sub-relatadas. Assim, esse estudo indagou se o sintoma de xerostomia na DECHc é decorrente de alterações morfológicas e funcionais das glândulas salivares. Para responder essa pergunta analisamos de forma qualitativa e por meio da morfometria, espécimes de biopsias de glândulas salivares labiais de pacientes com DECHc e com sintoma de xerostomia. Foram utilizados como controles, espécimes de biopsias de glândulas salivares de pacientes diagnosticados com Síndrome de Sjögren (SSp) (que é um modelo clássico de xerostomia) e de pacientes com líquen plano oral (LPO) (cujas manifestações clínicas orais podem se assemelhar às da DECHc) e queixa de xerostomia. Também foram analisadas, por meio de ensaio multiplex, as citocinas relacionadas à resposta imune Th17 (importante via imunológica na patogenia da DECHc) na saliva de 21 pacientes de DECHc, 27 de SSp, 10 de LPO e 15 voluntários saudáveis. Os principais achados morfológicos nas glândulas salivares dos pacientes de DECHc foram a extensa fibrose, fibroplasia periductal, atrofia ductal e acinar; alterações vasculares representadas pela congestão e formação de trombos hialinos; e infiltrado inflamatório intersticial difuso de aspecto leve a moderado. As glândulas salivares de SSp, entretanto, apresentaram um infiltrado inflamatório na forma de focos de linfócitos ao redor dos ductos excretores de intensidade moderada a severa; os ductos excretores apresentaram-se atróficos, ectásicos, exibindo metaplasia oncocítica e fibroplasia periductal; as alterações vasculares, por sua vez, se apresentaram em maior proporção na forma de vasculite. No LPO as alterações teciduais foram menos intensas. Quando analisadas as concentrações das citocinas, na DECHc, foram encontradas maiores concentrações de IL-17A, IL-4, IL-17F e IL-10, em relação aos grupos controles, essas citocinas estão envolvidas em mecanismos prófibróticos, o que permitiu a correlação dessa expressão aos eventos escleróticos nas glândulas salivares dos pacientes de DECHc. Entre elas, a IL-17F apresentou uma tendência de aumento em relação a proporção da área de fibrose nas glândulas salivares destes pacientes. A CD40L, que também esteve presente em maior concentração nos pacientes de DECHc, é uma molécula de ligação capaz de amplificar a resposta imunológica no mecanismo de rejeição do enxerto no hospedeiro, além de regular o mecanismo de apoptose e ativar o endotélio para a formação de trombos. As citocinas IL-31, IL-23 e IL-22, também apresentaram relevância na saliva dos pacientes de DECHc, sendo participantes do mecanismo das alterações liquenóides no LPO. Através das análises comparativas foi possível correlacionar a presença de citocinas envolvidas na resposta Th17 com as alterações glandulares e consequente xerostomia nos pacientes de DECHc.The graft versus host disease (GVHD) is one of the biggest causes of mortality and morbidity after hematopoietic stem cells transplantation. The pathophysiology in the chronical manifestation of the disease (cGVHD), is not entirely elucidated, however the involvement of the immunological system, by means of the innate and adaptive responses are depicted in the literature concerning the disease development. The cGVHD affects multiple organs, including the salivary glands, leading to xerostomia. These alterations are under reported and mostly unknown. Therefore, this study investigated if the symptom of xerostomia in cGVHD is triggered by functional e morphological changes in minor salivary glands. To answer this inquiry specimens of biopsied labial salivary glands from patients of cGVHD and xerostomia were analyzed qualitatively and through morphometry. Specimens of biopsied salivary glands from patients with Sjögren\'s Syndrome (SS) (which is a classic model of xerostomia) and from patients with oral lichen planus (OLP) (whose clinical oral manifestations resemble the cGVHD lesions) were used as controls. Also, the cytokines related to the immunological response Th17 (important immune pathway in cGVHD pathophysiology) in the saliva of 21 cGVHD patients, 27 of SS, 10 patients of OLP and 165 healthy individuals were analyzed using the multiplex assay. The major morphological findings revealed on the salivary glands of cGVHD patients were the extensive fibrosis, periductal fibrosis, ductal and acinar atrophy. Congestion and hyaline thrombi formation were the most important vascular changes shown among these specimens. A diffuse interstitial inflammatory infiltrate was observed, with varied intensity. The SS salivary glands, however, portrayed a focal inflammatory infiltrate, with moderate to severe intensity around the excretory ducts. These ducts exhibited atrophy, ectasia, periductal fibrosis and oncocytic metaplasia. The main vascular change presented in these patients was the manifestation of vasculitis. The salivary glands from the OLP patients showed a lesser amount of alterations. The multiplex assay revealed a higher concentration of the cytokines IL-17A, IL-4, IL-17F and IL-10 in the cGVHD samples, when compared to the other groups. These cytokines are involved within the promotion of fibrosis, which endorsed the association of these secretions with the salivary glands sclerotic mechanisms. The secretion of CD40L was higher in cGVHD samples; this membrane protein is capable of amplifying the immunological response in graft rejection, besides the capacity to regulate apoptosis and activate the endothelium in thrombi formation. The cytokines IL-31, IL-23 and IL-22, also presented a higher concentration in cGHVD patients\' saliva, these secretions are actively involved in the mechanisms of lichenoid lesions in OLP, corroborating the perceived morphological changes. The comparative analysis of the morphological and salivary changes in cGVHD confirmed the correlation of Th17 immunological response within the minor salivary glands injuries and consequent xerostomia in these patients.
41
Rietdorf, Katja. "Wirkungen biogener Amine auf die Erregungs-Sekretions-Kopplung in der Speicheldrüse von Periplaneta americana (L.)." Phd thesis, Universität Potsdam, 2003. http://opus.kobv.de/ubp/volltexte/2005/91/.
Full textAbstract:
In der vorliegenden Arbeit habe ich wichtige Teilmechanismen der Erregungs-Sekretionskopplung in der Speicheldrüse der Schabe Periplaneta americana (L.) untersucht. Die Speicheldrüse ist von dopaminergen und serotonergen Fasern innerviert (Baumann et al., 2002). Beide Transmitter stimulieren eine unterschiedliche Reaktion der Drüse: Dopamin (DA) stimuliert die P-Zellen der Acini und die Ausführgangzellen, während Serotonin (5-HT) die P- und C-Zellen der Acini stimuliert, nicht jedoch die Ausführgangzellen. Der Endspeichel ist nach einer DA-Stimulierung proteinfrei. Dagegen enthält er nach einer 5-HT-Stimulierung Proteine, die von den C-Zellen sezerniert werden (Just & Walz, 1996).
Im ersten Teil meiner Arbeit habe ich mittels Kapillarelektrophoretischer Analyse (CE-Analyse) die Elektrolytkonzentrationen im Endspeichel untersucht sowie die Raten der Flüssigkeitssekretion gemessen. Damit wollte ich klären, welche Transporter an der Sekretion des Primärspeichels und an dessen Modifikation beteiligt sind. Ausserdem wollte ich die Rolle der transportaktiven Epithelzellen der Ausführgänge für die Modifikation des Primärspeichels untersuchen. Dafür habe ich einen Vergleich der Elektrolytkonzentrationen im DA- und 5-HT-stimulierten Endspeichel durchgeführt. Der Elektrolytgehalt des DA- und 5-HT-stimulierten Endspeichels unterscheidet sich nicht signifikant voneinander. Er ist nach beiden Stimulierungen hypoosmotisch zum verwendeten Ringer. Die Ausführgangzellen werden durch DA stimuliert und modifizieren den Primärspeichel durch eine netto-Ionenreabsorption. Meine Versuche zeigen jedoch, dass auch die während einer 5-HT-Stimulierung der Drüse unstimulierten Ausführgangzellen den Primärspeichel modifizieren. In einer nachfolgenden Versuchsreihe habe ich den Einfluss von Ouabain, einem Hemmstoff der Na+-K+-ATPase, und Bumetanid, einem Hemmstoff des NKCC, auf die Raten der Flüssigkeitssekretion sowie den Elektrolytgehalt des Endspeichels untersucht. Ich habe gefunden, dass die Aktivität der Na+-K+-ATPase wichtig für die Modifikation des DA-stimulierten Primärspeichels ist. Im Gegensatz dazu ist sie für die Modifikation des 5-HT-stimulierten Primärspeichels nicht von Bedeutung. Bezüglich der Flüssigkeitssekretion habe ich keinen Einfluss der Na+-K+-ATPase-Aktivität auf die DA-stimulierten Sekretionsraten gefunden, dagegen ist die 5-HT-stimulierte Sekretionsrate in Anwesenheit von Ouabain gesteigert. Die Aktivität des NKCC ist für beide sekretorische Prozesse, die Ionen- und die Flüssigkeitssekretion, wichtig. Eine Hemmung des NKCC bewirkt eine signifikante Verringerung der Raten der Flüssigkeitssekretion nach DA- und 5-HT-Stimulierung sowie in beiden Fällen einen signifikanten Abfall der Ionenkonzentrationen im Endspeichel.
Im zweiten Teil meiner Arbeit habe ich versucht, Änderungen der intrazellulären Ionenkonzentrationen in den Acinuszellen während einer DA- oder 5-HT-Stimulierung zu messen. Diese Experimente sollten mit der Methode des "ratiometric imaging" durchgeführt werden. Messungen mit dem Ca2+-sensitiven Fluoreszenzfarbstoff Fura-2 zeigten keinen globalen Anstieg in der intrazellulären Ca2+-Konzentration der P-Zellen. Aufgrund von Problemen mit einer schlechten Beladung der Zellen, einer starken und sich während der Stimulierung ändernden Autofluoreszenz der Zellen sowie Änderungen im Zellvolumen wurden keine Messungen mit Na+- und K+-sensitiven Fluoreszenzfarbstoffen durchgeführt.
Im dritten Teil dieser Arbeit habe ich die intrazellulären Signalwege untersucht, die zwischen einer 5-HT-Stimulierung der Drüse und der Proteinsekretion vermitteln. Dazu wurde der Proteingehalt im Endspeichel biochemisch mittels eines modifizierten Bradford Assay gemessen. Eine erstellte Dosis-Wirkungskurve zeigt, dass die Rate der Proteinsekretion von der zur Stimulierung verwendeten 5-HT-Konzentration abhängt. In einer Serie von Experimenten habe ich die intrazellulären Konzentrationen von Ca2+, cAMP und / oder cGMP erhöht und anschließend den Proteingehalt im Endspeichel gemessen. Ein Anstieg der intrazellulären Ca2+-Konzentration aktiviert nur eine geringe Rate der Proteinsekretion. Dagegen kann die Steigerung der intrazellulären cAMP-Konzentration eine stärkere Proteinsekretion aktivieren, die sich nicht signifikant von der nach 5-HT-Stimulierung unterscheidet. Die cAMP-stimulierte Proteinsekretion kann durch gleichzeitige Erhöhung der intrazellulären Ca2+-Konzentration weiter gesteigert werden. Dagegen aktivierte eine Erhöhung der intrazellulären cGMP-Konzentration die Proteinsekretion nicht. Aufgrund dieser Ergebnisse postuliere ich die Existenz eines die Adenylatcyclase aktivierenden 5-HT-Rezeptors in der Basolateralmembran der C-Zellen.The aim of this PhD-work was to investigate major mechanisms of excitation-secretion coupling in the salivary gland of the cockroach Periplaneta americana (L.). This salivary gland is innervated by dopaminergic and serotonergic fibres (Baumann et al., 2002). The two transmitters stimulate different processes in the gland: Dopamine (DA) stimulates the p-cells of the acini and the salivary duct cells, whereas 5-HT (serotonin) activates the p- and the c-cells of the acini, but not the salivary duct cells. Final saliva is completely protein-free after dopamine stimulation. It contains proteins, which are secreted by the c-cells of the acini, after a 5-HT-stimulation (Just & Walz, 1996). In the first part of my work I measured the electrolytic composition of the final saliva by capillary electrophoretic analysis and measured the rates of fluid secretion, in order to answer the following questions: 1.) Which transporters affect the production of primary saliva and its modification? 2.) What is the function of the transport-active salivary duct cells for the modification of the primary saliva? Electrolytic composition of the DA- and 5-HT-stimulated final saliva is not significantly different from each other, and is hypoosmotic to the Ringer used. Salivary duct cells are stimulated by DA and modify the primary saliva by a netto ion-reabsorption. My experiments also show that the duct cells, which are unstimulated during a 5-HT-stimulation of the gland, modify the primary saliva. In the next series of experiments I investigated the effects of ouabain, an inhibitor of the Na+-K+-ATPase, and bumetanide, an inhibitor of the NKCC on the rates of fluid secretion and the electrolytic composition of the final saliva. I found, that the activity of the Na+-K+-ATPase is important for the modification of DA-stimulated primary saliva during its flow through the stimulated duct system. In contrast, it is not important for modification of the 5-HT-stimulated primary saliva. Inhibition of the Na+-K+-ATPase does not affect rates of DA-stimulated fluid secretion, but it increases the rates of 5-HT-stimulated fluid secretion. Activity of the NKCC is important for both secretory processes: the ion and the fluid secretion. Inhibition of the NKCC results in a significant drop in the rates of fluid secretion after DA- and 5-HT-stimulation, as well as a drop in electrolytic concentrations in the saliva. In the second part of my work, I tried to measure changes in the intracellular ionic concentrations (Ca2+, Na+, and K+) within the acinar cells during a DA- or 5-HT-stimulation. The experiments should be performed by ratiometric imaging. Measurements with the Ca2+-sensitive dye Fura-2 did not show any global increase in the intracellular Ca2+-concentration in the p-cells of the acini. Problems concerning a bad loading of the cells, a strong autofluorescence which changed during the time course of the stimulation, as well as changes in the cell volume were the reason, that no measurements using Na+- or K+-sensitive dyes were performed. In the third part of my work I investigated the intracellular signalling pathways, which activate protein secretion after 5-HT-stimulation of the gland. A modified Bradford Assay was used for measuring the protein content in the final saliva. In a dose-response curve I showed that rates of protein secretion are dependent on the 5-HT-concentrations used to stimulate the glands. In another set of experiments I increased the intracellular concentrations of Ca2+, cAMP and / or cGMP, and measured the protein content in the final saliva. An increase in the intracellular Ca2+-concentration activates only a low rate of protein secretion. After an increase in the intracellular cAMP-concentration a much higher rate of protein secretion can be activated, which is not significantly different from the 5-HT stimulated rate of protein secretion. The cAMP-stimulated protein secretion can be further increased by a simultaneous rise in the intracellular Ca2+-concentration. In contrast, cGMP does not activate protein secretion. Therefore I propose the expression of an adenylyl cyclase activating 5-HT-receptor in the basolateral membrane of the protein secreting c-cells.
42
Lamers, Marcelo Lazzaron. "Concentração elevada de glicose e interação célula-matriz extracelular: efeitos sobre a homeostase de glândulas salivares, adesão e migração celular." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-11112008-131435/.
Full textAbstract:
Neste estudo avaliou-se os efeitos do diabetes mellitus (DM) sobre dois sistemas: glândula parótida de ratos e células cultivadas in vitro. Foram avaliados respectivamente a composição da matriz extracelular e a migração de células expostas a elevada concentração de glicose. Na parótida observou-se aumento de colágenos III, IV e V, laminina e fibronectina, mediado por TGFb2. Em células isoladas observou-se que a glicose dificultou a polarização celular, reduziu a velocidade e direcionalidade de migração, reduziu a persistência e estabilidade das protrusões celulares e a maturação de adesões. Estas alterações estão relacionadas à ativação da GTPase Rac1, dependente de estresse oxidativo. Este estudo sugere, pela primeira vez, que: 1) a hipofunção salivar pode envolver um espessamento da lâmina basal de capilares e parênquima por mecanismos previamente observados em outros orgãos-alvo de complicações diabéticas e 2) que a glicose exerce um efeito direto sobre a migração celular, fator que pode contribuir para a cicatrização deficiente em indivíduos diabéticos.In this study we evaluated the effects of DM on two different systems: the rat parotid gland and in vitro cultured cells. Extracellular matrix composition and the migratory behavior of cells exposed to a high glucose concentration (HG) were evaluated, respectively. In the parotid, DM led to an increase in collagens III, IV and V, laminin and fibronectin, through a TGFb2-dependent mechanism. In cultured cells, HG impaired cell polarization, reduced migration velocity and directionality, reduced the persistence and stability of protrusive cellular processes, as well as adhesion maturation. These effects were related to Rac1 GTPase activation, dependent on the oxidative stress promoted by HG. This study suggests, for the first time, that: 1) salivary hypofunction in DM might involve the thickening of capillary and parenchyma basal lamina, through mechanisms already described in other target organs for diabetic complications and 2) that glucose directly impairs cell migration, and this effect may contribute to the chronic wound healing observed in diabetic patients.
43
Ramos, Anderson Daniel. "Imunomodulação da encefalomielite autoimune experimental pelo extrato da glândula salivar de Aedes aegypti." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-12122014-124408/.
Full textAbstract:
A saliva de insetos hematófagos possui moléculas capazes de modular o sistema imune do hospedeiro. Com base na literatura a respeito das atividades presentes na saliva de Aedes aegypti, investigamos se o EGS dessa espécie era capaz de modular a EAE. Imunizamos animais C57BL/6 com MOG35-55, e realizamos um tratamento com EGS. O tratamento com EGS diminuiu a incidência da doença e provocou um atraso no aparecimento dos sinais clínicos, além de estes serem mais brandos. Observamos que a modulação se deu na fase de indução da resposta imune, não na efetora. De fato, o EGS consegue suprimir a doença por 4 vias: 1) diminuindo a expressão de MHCII, CD80 e CD86 em células dendríticas, e diminuindo a produção de citocinas responsáveis pela indução das respostas Th1/Th17; 2) induzindo células produtoras de IL-10 in vivo; 3) induzindo apoptose em linfócitos T naive; 4) induzindo células com perfil Th2 produtoras de IL-4 e IL-5. Concluímos que o EGS é capaz de atuar na supressão dos sintomas durante o curso da EAE e na inibição do início da resposta imune.The saliva of hematophagous insects has molecules that can modulate the host immune system. Based on the literature about activities found in Aedes aegypti saliva, we investigate if SGE of this species could modulate EAE. We have immunized C57BL/6 mice with MOG35-55, and carried out a treatment with SGE. The treatment with SGE reduced the incidence of disease and caused a delay onset of clinical signs making them softer. We have observed that modulation occured in the induction phase of immune response, not in effector phase. In fact, SGE can suppress the disease by four ways: 1) decreasing the expression of MHCII, CD80 and CD86 in dendritic cells and decreasing the production of cytokines responsible for Th1/Th17 response induction; 2) inducing cells producing IL-10 in vivo; 3) inducing apopotosis in naive T lymphocytes; 4) inducing cells Th2 producing IL-4 e IL-5. We came to the conclusion that SGE can act in supressing symptoms during the course of EAE and inhibiting the beggining of autoimmune response.
44
Souza, Gabriely Köerich. "Morfologia de ovos, glândulas salivares e sistemas digestivo e reprodutor de Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae)." Universidade Federal de Viçosa, 2012. http://locus.ufv.br/handle/123456789/3961.
Full textAbstract:
Made available in DSpace on 2015-03-26T13:30:43Z (GMT). No. of bitstreams: 1
texto completo.pdf: 3355723 bytes, checksum: 62b4b87ccb61cdcbdc48ea8e77a66ee5 (MD5)
Previous issue date: 2012-07-26Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
The bronze bug Thaumastocoris peregrinus Carpintero & Dellapé (Hemiptera: Thaumastocoridae) is a pest of Corymbia and Eucalyptus species and there are no effective strategies for its control in commercial plantations. Biological data of insects of the family Thaumastocoridae are scarce, mainly with species of the subfamily Xylastodorinae. Morphological studies of eggs and digestive and reproductive systems can provide important information to control T. peregrinus. This study described the morphology of eggs, salivary glands, alimentary canal and reproductive systems of males and females T. peregrinus. Thirty females and fifteen males of T. peregrinus with different ages were obtained from a mass rearing facility in a room with temperature at 25 ± 2ºC, 70 ± 10% RH and 12 h photophase and prepared for analysis in a light microscopy. Eggs of T. peregrinus were obtained from the mass rearing facility, coated with gold and analyzed in a scanning electron microscope. Thaumastocoris peregrinus has a pair of bilobed principal salivary glands located between the segments of the meso- and metathorax. The wall of the lobes is formed by a single layer of cubic cells with some of them binucleate. Each gland has a main duct formed by a single layer of flattened cells. The alimentary canal of T. peregrinus has a short faringe followed by a long and thin esophagus that ends in a simple proventriculus and a short estomodeal valve. The midgut of T. peregrinus comprises an anterior dilated region without gastric cecae, a long and narrow middle region and a short and dilated posterior one. The hindgut is composed by a transition region with the midgut where the insertion of two pairs of Malpighian tubules occurs, a short ileum and a rectum with a folded epithelial wall, thick cuticle and flattened cells. The male reproductive system of T. peregrinus is formed by a pair of testa with three large and globular follicles isolated by a peritoneal sheath and two pairs of tubular mesadenian accessory glands well developed. The female reproductive system of T. peregrinus is formed by a pair of ovaries with two meroistic telotrophic ovarioles each. The ovarioles open into two long lateral oviducts that join into a short common oviduct. The common oviduct ends in a large bursa copulatrix with many folds and both are lined by a thick cuticle. Eggs with embryos at the stages of anatrepsis, katatrepsis and also after the dorsal closure were observed in the reproductive tract of T. Peregrinus females. Eggs of T. peregrinus are oval-shaped and flattened dorso-ventrally with a strong depression in the center and black colored. The chorion of the egg is divided into exochorion, endochorion, air layer and an inner chorionic layer. The outer surface of the exochorion lacks perforations or pores and showed shallow and elongated depressions that were more circular in the posterior region of the egg. The opercular opening is located laterally in the eggs of T. peregrinus with the neck region showing around 27 circular and concave projections that appear to be aeromicropyles, reduced chorionic rim and a narrow sealing bar internally. The operculum is elliptical and flattened and has the same texture as the rest of the corium, except for the smooth texture of the outer opercular region. Thaumastocoris peregrinus has digestive and reproductive systems similar to other species of Thaumastocoridae, but the external characteristics of the eggs of this species differ from others of the same family. Studies of a larger number of species can contribute to the knowledge and importance of the structures evaluated for identifications at the level of subfamily, genus or species and to understand the phylogenetic relationships of Thaumastocoridae.
O percevejo bronzeado Thaumastocoris peregrinus Carpintero & Dellapé (Hemiptera: Thaumastocoridae) é praga de espécies de Corymbia e Eucalyptus e não existem estratégias eficientes para seu controle em plantios comerciais. Dados biológicos de insetos da família Thaumastocoridae são escassos, sendo, principalmente,com espécies da subfamília Xylastodorinae. Estudos morfológicos dos ovos e sistemas digestivo e reprodutor podem fornecer informações para o controle de T. peregrinus. Este estudo descreveu a morfologia dos ovos, das glândulas salivares, do canal alimentar e dos sistemas reprodutores de machos e fêmeas de T. peregrinus. Trinta fêmeas e quinze machos de T. peregrinus com diferentes idades foram obtidos de criação massal em sala climatizada à temperatura de 25 ± 2oC, 70 ± 10% de UR e fotofase de 12 horas e preaparados para análise em microscópio de luz. Ovos de T. peregrinus foram obtidos da criação massal, metalizados com ouro e analisados em microscópio eletrônico de varredura. Thaumastocoris peregrinus possui um par de glândulas salivares principais bilobadas entre os segmentos do meso e metatórax. As paredes dos lóbulos são formadas por uma camada simples de células cúbicas sendo algumas binucleadas. Cada glândula possui um ducto principal formado por uma camada simples de células achatadas. O canal alimentar de T. peregrinus é formado por uma faringe curta seguida por um esôfago longo e fino terminando em um proventrículo simples e uma válvula estomodeal curta. O intestino médio de T. peregrinus é composto por uma região anterior dilatada e sem cecos gástricos, uma região mediana longa e estreita e outra posterior curta e dilatada. O intestino posterior é composto por uma região de transição com o intestino médio onde ocorre a inserção de dois pares de túbulos de Malpighi, um curto íleo e um reto com parede epitelial com grande quantidade de dobras, cutícula espessa e células achatadas. O sistema reprodutor masculino de T. peregrinus é formado por um par de testículos com três folículos grandes e globulares isolados por uma bainha peritoneal e dois pares de glândulas acessórias mesadênias tubulares e bem desenvolvidas. O sistema reprodutor feminino de T. peregrinus é formado por um par de ovários com dois ovaríolos cada do tipo meroístico telotrófico. Os ovaríolos abrem-se em dois ovidutos laterais longos que se unem em um oviduto comum curto. O oviduto comum termina em uma bursa copulatrix ampla e com diversas dobras e ambos são revestidos por uma cutícula espessa. Ovos com embriões nos estágios de anatrepsis, catatrepsis e após o fechamento dorsal foram observados no trato reprodutivo de fêmeas de T. peregrinus. A forma dos ovos de T. peregrinus é oval e achatada dorso-ventralmente com forte depressão no centro e coloração preta. O cório do ovo é dividido em exocório, endocório, camada de ar e camada coriônica interna. A superfície externa do exocório apresentou depressões pouco profundas e alongadas ou com formato mais circular na região posterior do ovo sem perfurações ou poros. A abertura opercular é localizada lateralmente no ovo de T. peregrinus com a região do colo apresentando em torno de 27 projeções circulares côncavas que parecem ser aeromicrópilas, borda corial reduzida e, internamente, uma faixa de vedação estreita. O opérculo é elíptico e achatado e apresenta textura semelhante ao restante do cório, exceto pela textura lisa da região mais externa. Thaumastocoris peregrinus possui sistemas digestivos e reprodutor semelhantes a outras espécies de Thaumastocoridae, mas as características externas dos ovos diferiram das demas espécies dessa família. Estudos de um maior número de espécies poderão contribuir para o conhecimento e importância das estruturas avaliadas para identificações em nível de subfamília, gênero ou espécie e se compreender as relações filogenéticas de Thaumastocoridae.
45
Oliveira, Elaine Cyreno. "Adesão e atividade de protease são reguladas pelo peptídeo derivado da laminina AG73, sindecan-1 e integrina 1 em linhagem celular derivada de carcinoma adenóide cístico." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-09022010-105201/.
Full textAbstract:
Estudamos indução da atividade de MMP pelo peptídeo da laminina a1 AG73 em linhagem celular (CAC2) de carcinoma adenóide cístico. CAC2 cultivadas em laminina-111 com AG73 geraram espaços pseudocísticos. Inibidor de MMP diminuiu tais espaços, sugerindo ação de MMPs. CAC2 crescidas sobre AG73 mostraram aumento dose-dependente de MMP9. RNAi para MMP9 diminuiu remodelação em cultura 3D. Buscamos receptores de AG73 ligados à atividade de MMP9. CAC2 crescidas sobre AG73 exibiram colocalização de sindecan-1 e integrina b1. RNAi para sindecan-1 ou para integrina b1 geraram, isolados, redução na adesão a AG73 e nas atividades de remodelação e de protease. Duplo RNAi estudou a cooperação entre os receptores e promoveu diminuição na adesão a AG73 e na atividade de MMP. Distinção de receptores foi feita por cromatografia de afinidade e espectrometria de massa, através de colunas de afinidade com AG73 acoplado, que resultou em possíveis receptores, como integrinas b1 e aV. Sugerimos que AG73 regula adesão e secreção de MMP em células CAC2 através de sindecan-1 e integrina b1.We studied induction of MMP activity by b1-laminin peptide AG73 in adenoid cystic carcinoma cell line (CAC2). Cells grown inside AG73-enriched laminin-111 exhibited pseudocystics spaces. MMP inhibitor decreased those spaces, suggesting MMPs action. Cells grown on AG73 showed a dose-dependent increase of MMP9 secretion. MMP9 siRNAi decreased remodeling in 3D culture. We searched for AG73 receptors regulating MMP9 activity. CAC2 grown on AG73 exhibited colocalization of syndecan-1 and b1 integrin. Syndecan-1 siRNA or siRNA b1 integrin showed reduction in adhesion to AG73 and in remodeling and protease activities. Double-knockdown explored syndecan-1 and 1 integrin cooperation and showed decrease in adhesion to AG73 and in MMP activity. Receptors characterization was made by affinity chromatography followed by mass spectrometry through AG73-affinity columns and showed putative receptors, like b1 and aV integrins. We suggest that AG73 peptide regulates adhesion and MMP secretion in CAC2 cells through syndecan-1 and b1 integrin.
46
Miguel, M?rcia Cristina da Costa. "Express?o imuno-histoqu?mica das integrinas a2?1, a3?1 e a5?1 em adenoma pleom?rfico de gl?ndula salivar menor e maior e carcinoma aden?ide c?stico." Universidade Federal do Rio Grande do Norte, 2005. http://repositorio.ufrn.br:8080/jspui/handle/123456789/17167.
Full textAbstract:
Made available in DSpace on 2014-12-17T15:32:33Z (GMT). No. of bitstreams: 1
MarciaCCMiguel_tese.pdf: 1534160 bytes, checksum: 1a3ec415bfaf10c088ec1ae5f6224189 (MD5)
Previous issue date: 2005-05-27Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico
Pleomorphic adenoma and adenoid cystic carcinoma (ACC) consist benign and malignant neoplasm from salivary gland, respectively. These neoplasms share some characteristics, such as cellular origin and considerable production of extracellular matrix, however, with distinct biological behavior. The aim of the present study was to compare the expression of D2E1, D3E1 e D5E1 integrins in pleomorphic adenoma from minor and major salivary glands and ACCs. Furthermore, it was investigated possible differences in the expression of these integrins according to histological subtypes of ACC. Fourteen cases of pleomorphic adenoma from major salivary gland, fourteen cases from minor salivary gland and ten cases of ACC were selected. It was taken into consideration the presence or absence, localization and intensity of integrin immunoexpression. The cases of pleomorphic adenoma were grouped in order to compare the expression between the distinct neoplasms. It was observed a highly significant difference (p<0,0001) in relation to D2E1 integrin between the neoplasms since pleomorphic adenoma showed a pronounced immunostaining. It was not possible to perform statistical tests considering the D2E1 integrin expression; nevertheless, it could be observed a tendency of higher staining in pleomorphic adenoma. For comparative reasons the cases ACCs were divided in two groups: solid and tubular/cribriform. It was not detected significant differences in regard to D2E1 integrin; and statistical analysis could not be realized in relation to D3E1 and D5E integrin expression. However, it was also verified a tendency of absence or reduced expression in the solid subtype. It can be concluded that the reduced D2E1 integrin expression observed in CACs may be related to a lesser degree of cell differentiation in this neoplasm and the reduced D5E1 integrin expression can be associated with aggressive biological behavior. Moreover, the absence and/or reduced expression of the studied integrins in solid ACC suggests a role in pathogenesis and more aggressive biological behavior of this histological subtype
O adenoma pleom?rfico e o carcinoma aden?ide c?stico (CAC) representam neoplasias de gl?ndula salivar benigna e maligna, respectivamente, as quais compartilham algumas caracter?sticas como a mesma origem celular e uma marcante presen?a de matriz extracelular, apresentando, por?m, comportamentos biol?gicos distintos. O prop?sito desta pesquisa consistiu em comparar a express?o das integrinas D2E1, D3E1 e D5E1 em adenomas pleom?rficos de gl?ndula salivar menor e maior e CACs. Al?m disso, procurou investigar se havia diferen?as na express?o destas integrinas entre os subtipos histopatol?gicos do CAC. Foram selecionados 14 casos de adenoma pleom?rfico de gl?ndula salivar maior, 14 casos de gl?ndula salivar menor e 10 casos de CACs. Analisou-se a presen?a ou aus?ncia, localiza??o e intensidade de marca??o das integrinas. Os dois grupos de adenomas pleom?rficos foram reunidos em um s? para fazer a compara??o entre os dois tumores. Verificou-se que houve diferen?a estat?stica altamente significativa (p<0,0001) para a integrina D2E1 entre os dois tumores, apresentando o adenoma pleom?rfico, uma marca??o mais intensa para esta integrina. Em rela??o ? integrina D5E1 n?o foi poss?vel a realiza??o de testes estat?sticos, ficando patente, por?m, que houve uma tend?ncia da referida integrina ser mais intensamente expressa no adenoma pleom?rfico. Para an?lise comparativa, os CACs foram subdivididos em 2 grupos: s?lido e tubular/cribriforme. Para a integrina D2E1 observou-se que n?o houve diferen?a estatisticamente significativa e em rela??o ? D3E1 e D5E1 n?o foi poss?vel a realiza??o do teste estat?stico; no entanto, tamb?m foi verificada uma clara tend?ncia para os casos do subtipo s?lido apresentarem express?o ausente ou reduzida das integrinas avaliadas. Concluiu-se que a reduzida express?o da integrina D2E1 observada nos CACs, pode estar relacionada com a menor diferencia??o das c?lulas deste tumor e ? poss?vel que a reduzida express?o da D5E1, possa estar implicada em seu comportamento mais agressivo. Al?m disso, sugere-se que a aus?ncia e/ou redu??o da express?o das integrinas pesquisadas nos casos do subtipo s?lido, pode desempenhar algum papel na patog?nese e no comportamento biol?gico mais agressivo deste subtipo tumoral
47
Fernandes, K?tia Roberta. "Biologia, Diagn?stico morfol?gico e molecular da infec??o experimental e natural de Babesia equi (Laveran, 1901) em Boophilus microplus (Canestrini, 1887)." Universidade Federal Rural do Rio de Janeiro, 2007. https://tede.ufrrj.br/jspui/handle/tede/819.
Full textAbstract:
Made available in DSpace on 2016-04-28T20:16:24Z (GMT). No. of bitstreams: 1
2007- Katia Roberta Fernandes.pdf: 2143619 bytes, checksum: 6ff7127f4642317cf1f53d7aceb93f1f (MD5)
Previous issue date: 2007-02-26Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior
The aim of the present study was to evaluate the natural and experimental infection of B. equi in nymphs and adult Boophilus microplus using optical microscopy and molecular analysis. The experimental infection was observed in nymphs, males and females of B. microplus fed on equines chronically infected with B. equi and in non fed larvae and eggs. For the experiments two equines, of not defined breed, proven to be infected with B. equi were used. The animals were infested with B. microplus larvae of generation F4 obtained from a laboratory maintained population, known to be free of Babesia spp. infection. Daily collections of ticks were realized using as starting point the ecdisys to nymph state. After the collection the hemolymph was examined and the intestine and salivary glands were dissected, smashed on glass slides for microscopy, methanol treated and stained with Giemsa. There were dissected 860 specimens (432 nymphs, 280 females and 148 males). The dissected salivary glands were divided into two parts. The first one was smashed on microscopy glass slides, stained and examined by optical microscopy for morphologic analyses. From the second part was realized DNA extraction and PCR with specific primers for the 18S rRNA. On optical microscopy of nymph hemolymph was possible to be observed the presence of kinetes with claviform aspect characteristic for the genus Babesia. In the salivary glands of B. microplus nymphs the morphology and the sequence of developmental stages of B. equi were observed initiating on day 4 after ecdysis, being possible to see in acinary cells the formation of sporoblasts and ovoid sporozoites measuring 1.5 μm of diameter and elongated sporozoites with 3.8 to 5.2μm of length and 0.8 to 1.5 μm of width. The PCR confirmed the presence of B. equi in DNA samples extracted from salivary glands of nymphs, male and female ticks as well as in larvae and eggs. To evaluate the natural infection were collected nymphs and adult B. microplus from two equines naturally infested by these ticks and naturally infected with B. equi. These horses were originated from Seropedica city in the state of Rio de Janeiro. There were dissected 324 specimens (145 nymphs, 138 females and 41 males). The proceedings with the salivary glands were identical to the previously described for the experimental infection. Of the salivary glands submitted to PCR, 70% showed to be infected with B. equi. Microscopical analysis of the salivary glands revealed the presence of sporoblast stages and the development of elongated sporozoites in acinary glands. The morphologic, morphometric and molecular analysis confirmed the experimental and natural infection of the salivary glands of nymphs and adult B. microplus with B. equi. The results of the present study show the ability of B. equi to develop in this tick species. The detection of B. equi DNA in eggs and larvae also suggests the possibility of transovarian transmission in B. microplus. The results allow to consider the tick B. microplus as a potential biologic vector of B. equi in horses from the studied region.
Este trabalho teve como objetivo avaliar a infec??o natural e experimental de Babesia equi em ninfas e adultos de Boophilus microplus por meio de microscopia ?ptica e an?lise molecular. A infec??o experimental foi observada a partir de ninfas, machos, f?meas, ovos e larvas n?o alimentadas de B. microplus alimentados em equinos com infec??o cr?nica por B. equi. Para a realiza??o do experimento foram utilizados dois eq?inos, mesti?os, com infec??o por B. equi. Os animais foram infestados com larvas de B. microplus de gera??o F4 obtidas de col?nia mantida em laborat?rio e livres de infec??o por Babesia spp. A partir da ecdise para ninfa foram realizadas coletas di?rias. Ap?s a coleta foram realizados os exames de hemolinfa e extra??o do intestino e das gl?ndulas salivares os quais foram macerados em l?minas de vidro para microscopia, fixados em metanol e corados com Giemsa. As gl?ndulas salivares dissecadas foram divididas em duas partes. A primeira parte foi macerada em l?minas de vidro para microscopia, corada com corante Giemsa e observada em microsc?pio ?tico para an?lise morfol?gica. A segunda parte foi realizada a extra??o de DNA, sendo submetida a PCR com primers especif?cos para o gene 18S rRNA para B. equi. Foram dissecados 860 esp?cimes (ninfas= 432; f?meas= 280 e machos= 148). Na microscopia ?ptica foi poss?vel observar nas hemolinfas das ninfas a presen?a de cinetos com aspecto claviforme t?picos do g?nero Babesia. Nas gl?ndulas salivares, a morfologia e a seq??ncia dos est?gios de desenvolvimento de B. equi das ninfa s de B. microplus, foram observadas a partir do 4? dia ap?s ecdise, sendo poss?vel observar nos ?cinos celulares a forma??o de esporoblastos e de esporozo?tas ov?ides medindo 1,5 μm de di?metro e alongados medindo 3,8 a 5,2μm de comprimento e 0,8 a 1,5μm de largura. A rea??o em cadeia de polimerase (PCR) confirmou a presen?a de B. equi em DNA de gl?ndulas salivares extra?das de ninfas, machos, f?meas, assim como dos ovos e larva. A infec??o natural foi observada a partir de ninfas e adultos de B. microplus coletados de dois eq?inos naturalmente infestados e comprovadamente infectados por B. equi, procedentes do munic?pio de Serop?dica, Rio de Janeiro. Foram dissecados 324 esp?cimes (ninfas= 145, f?meas= 138 e machos= 41). O processamento das gl?ndulas salivares dissecadas foi semelhante ao descrito para infec??o experimental. Das gl?ndulas salivares submetidas a PCR, 70% apresentaram resultados positivos para B. equi. As an?lises por microscopia ?ptica das gl?ndulas salivares das ninfas e dos adultos revelaram a presen?a nos ?cinos celulares os est?gios de esporoblastos e o desenvolvimento de esporozo?tas alongados. As an?lises morfol?gicas, morfom?tricas e moleculares confirmaram a infec??o experimental e natural das gl?ndulas salivares de ninfas e adultos de B. microplus por B. equi. Os resultados deste estudo demonstram a capacidade de multiplica??o de B. equi em gl?ndulas salivares de ninfas e adultos de B. microplus. A detec??o de DNA de B. equi em ovos e larvas de B. microplus tamb?m sugere a possibilidade da transmiss?o transovariana nesta esp?cie de carrapato. Estes resultados sugerem que o carrapato B. microplus ? vetor biol?gico de B. equi na regi?o estudada.
48
Lascane, Nelise Alexandre da Silva. "Expressão imuno-histoquímica das proteínas Jab1, p27, c-jun e c-fos no adenoma pleomórfico, adenocarcinoma polimorfo de baixo grau e carcinoma adenoide cístico das glândulas salivares." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/23/23141/tde-18032015-173058/.
Full textAbstract:
Os tumores de glândula salivar compreendem em torno de 2 a 6,5% dos tumores de cabeça e pescoço. Entre os tumores de glândula salivar, o adenoma pleomórfico é benigno e o mais comum. O carcinoma adenoide cístico e adenocarcinoma polimorfo de baixo grau encontram-se entre os mais frequentes malignos. Jab1 é uma de muitas proteínas que afetam diversos estágios da tumorigênese sendo importante na regulação variadas vias de sinalização e/ou proteínas como p27 e AP-1, a última composta por c-jun e c-fos, que são principalmente relacionadas com o ciclo celular e proliferação celular. O objetivo desse trabalho foi avaliar a expressão imuno-histoquímica das proteínas Jab1, p27, c-jun e c-fos no adenoma pleomórfico, adenocarcinoma polimorfo de baixo grau e carcinoma adenoide cístico das glândulas salivares. Foi realizada análise imuno-histoquímica semi-quantitativa das células marcadas nos tumores de glândula salivar e glândula salivar normal de acordo com o escore 0 (células sem expressão), 1(> 0 <= 5% de células marcadas), 2 (> 5 <= 50%) and 3 (> 50%). Para Jab1, c-jun e c-fos foi considerado apenas marcação nuclear e para p27, nuclear e citoplasmática, separadamente. Os resultados foram analisados utilizando-se os testes de Kruskal-Wallis, de Mann-Whitney, do Qui-quadrado e o teste de correlação de Spearman, cujo nível de significância foi de p<0,05 e processados com o auxílio do software GraphPad Prisma 5.0. A análise estatística revelou que a expressão de Jab1 foi significante no adenoma pleomórfico e no carcinoma adenoide cístico em relação aos ductos e no adenocarcinoma polimorfo de baixo grau em relação ao carcinoma adenoide cístico (p=0,0136, 0,0001 e 0,0344, respectivamente); a expressão de p27 nuclear foi significante no adenoma pleomórfico e no adenocarcinoma polimorfo de baixo grau quando comparados ao carcinoma adenoide cístico (p=0,0074 e 0,0004, respectivamente) e a expressão citoplasmática em todos os grupos quando comparados aos ácinos; c-fos, a expressão foi significativa nos ductos ao compará-los ao adenoma pleomórfico, adenocarcinoma polimorfo de baixo grau e carcinoma adenoide cístico (p=0,0002, 0,0048 e 0,0352, respectivamente). O teste de correlação de Spearman de Jab1, p27, c-jun e c-fos em cada lesão separadamente revelou que no adenoma pleomórfico houve correlação significativa entre Jab1 e p27 (r=0,371; p=0,020) e entre c-jun e c-fos (r=0,452; p=0,004). No adenocarcinoma polimorfo de baixo grau, houve correlação entre Jab1 e p27 (r=0,494; p=0,044) e no carcinoma adenoide cístico, entre p27 e c-fos (r=0,513; p=0,035). Foi concluído que a tumorigênese do adenoma pleomórfico, adenocarcinoma polimorfo de baixo grau e carcinoma adenoide cístico parece estar associada à expressão de Jab1 e p27.Salivary gland tumors comprise about 2 to 6.5% of the head and neck tumors. Among the salivary gland tumors, pleomorphic adenoma is the most common and benign tumor. Adenoid cystic carcinoma and polymorphous low-grade adenocarcinoma are the most frequent malignant tumors. Jab1 is one of many proteins which affects many stages of the tumorigenesis and regulates positively and negatively several pathways and/or proteins such as p27 and AP-1, the latter composed by c-jun and c-fos, which are mostly related to cell cycle and cell proliferation. The aim of this study was to evaluate the immunoexpression of the proteins Jab1, p27, c-jun and c-fos in pleomorphic adenoma, polymorphous low-grade adenocarcinoma and adenoid cystic carcinoma of the salivary glands. The semi-quantitative immunohistochemical analysis was performed in salivary gland tumors and in normal salivary gland according to the score 0 (no stained cells), 1 (> 0 <= 5% of stained cells), 2 (> 5 <= 50%) and 3 (> 50%). Nuclear immunostaining alone was considered for Jab1, c-jun and c-fos proteins and cytoplasmic and nuclear staining for p27. Results were analyzed in GraphPad Prisma 5.0 software using Kruskal-Wallis, Mann-Whitney and Chi-square tests and Spearman correlation test in which significancy level was p<0,05. Statistical analysis revealed that Jab1 expression was significant in pleomorphic adenoma and adenoid cystic carcinoma in relation to ducts and in polymorphous low-grade adenocarcinoma in relation to adenoid cystic carcinoma (p=0,0136, 0,0001 e 0,0344, respectively); the p27 nuclear expression was significant in pleomorphic adenoma and in polymorphous low-grade adenocarcinoma when compared to adenoid cystic carcinoma (p=0,0074 e 0,0004, respectively) and cytoplasmic immunostaining was significant in all groups when compared to acini; c-fos expression was significant in ducts if compared to pleomorphic adenoma, polymorphous low-grade adenocarcinoma and adenoid cystic carcinoma (p=0,0002, 0,0048 e 0,0352, respectively). Spearman correlation test to Jab1, p27, c-jun and c-fos in each lesion separately revealed significant correlation between Jab1 and p27 (r=0,371; p=0,020) and c-jun and c-fos (r=0,452; p=0,004) in pleomorphic adenoma. There was correlation between Jab1 and p27 (r=0,494; p=0,044) in polymorphous low-grade adenocarcinoma and between p27 and c-fos (r=0,513; p=0,035) in adenoid cystic carcinoma. In conclusion, tumorigenesis in pleomorphic adenoma, polymorphous low-grade adenocarcinoma and adenoid cystic carcinoma seems to be associated to expression of Jab1 and p27.
49
Hira, Priyesh Gunvant. "Buffering capacity of saliva, salivary flow rates and cortisol levels in patients with active caries." Thesis, 2013. http://hdl.handle.net/10539/12545.
Full textAbstract:
Introduction: Dental caries is caused by the interaction of the host, oral flora and diet. Stress is
one of the host factors implicated. Studies have shown that there is an association between
stress and salivary cortisol levels. However, no studies have investigated the relationship
between stress, salivary cortisol levels and caries susceptibility. Aims and objectives: The aim
of the study was to determine whether there is a correlation between active dental caries, resting
and stimulated flow of saliva, salivary buffering capacity, saliva cortisol levels and stress in
patients attending a general dental practice in Lenasia South. Methods and materials: Sixty
subjects between the ages of 18 and 60 were included in the study. Thirty controls with no active
caries, a minimum of 28 teeth and a mean decayed, missing filled surfaces (DMFS) score of 4 or
less, and 30 subjects with active caries were included in the study and formed the experimental
group. Patients with Sjögren’s Syndrome or connective tissue diseases, on medication that may
cause xerostomia, or a history of previous or current irradiation were excluded from the study. At
the initial visit resting and stimulated saliva samples were collected and the volume was
measured. The buffering capacity and cortisol levels of the resting saliva samples were
measured. In addition the Depression Anxiety Stress Scales (DASS) questionnaire was used to
determine the stress levels of the participants. The teeth of the subjects with active caries, i.e.
the experimental group, were restored. They returned after 4 weeks for a follow up visit and their
resting and stimulated salivary flow, buffering capacity of saliva, salivary cortisol and the stress
levels were measured. The results were compared using the two sample t test, chi – squared test
and a generalized logistic regression analysis. Results: The DMFS of the control group,
0.40 + 0.97, was significantly lower (p < 0.001) than 29.27 + 21.94, in the experimental group. No
significant differences were found between the controls and caries prone subjects when the
resting flow rates, 0.37 + 0.30 ml/min and 0.32 + 0.19 ml/min; stimulated flow rates,
0.99 + 0.56 ml/min and 0.84 + 0.35 ml/min; buffering capacity of saliva,
19.16 + 4.68 ml 0.01N lactic acid and 21.73 + 9.77 ml 0.01N lactic acid, were compared and the
salivary cortisol levels of the controls 17.71 + 22.51 ng/ml, were higher than 11.80 + 14.61 ng/ml
in the the caries prone subjects. The DASS scores of the two groups were similar,
i.e. 11.33 + 8.48 and 11.2 + 9.6, respectively. After the carious teeth of the caries prone subjects
were restored, the flow rate of resting saliva increased from 0.32 + 0.19 ml/min to
0.37 + 0.16 ml/min, the stimulated saliva from 0.84 + 0.35 ml/min to 0.88 + 0.32 ml/min and the
buffering capacity of saliva from 21.73 + 9.77 ml 0.01N lactic acid to 22.25 + 7.55 ml 0.01N lactic
acid and the salivary cortisol levels decrease from 11.80 + 14.61 ng/ml to 10.00 + 12.12 ng/ml.
Again none of these differences were significant. Conclusion: These results suggest that stress
levels measured by the DASS questionnaire may not be related to caries. A less subjective
questionnaire may find a relationship between salivary cortisol levels, stress and dental caries.
50
Mendes, Susete Maria Oliveira. "Hipossalivação: da etiologia ao tratamento." Master's thesis, 2017. http://hdl.handle.net/10284/6114.
Full textAbstract:
A sensação de boca seca pode ser subjetiva, designando-se por xerostomia ou estar associada a hipofunção das glândulas salivares (hipossalivação) ou alteração da composição salivar. São dois conceitos diferentes, apesar da sua utilização indiscriminada, muitas vezes subvalorizados e subdiagnosticados pelo médico dentista. A hipofunção das glândulas salivares predispõe os pacientes a diversas complicações como disgeusia, dor, sensação de ardor na mucosa oral, cáries dentárias e outras doenças infeciosas, disfagia e disfonia, queixas frequentes na consulta de medicina dentária. O objetivo deste trabalho é, à luz do conhecimento atual e recorrendo a pesquisa bibliográfica, compreender a etiologia, métodos de diagnóstico e estratégias terapêuticas para a gestão do paciente com hipossalivação e xerostomia. A gestão do tratamento do paciente com hipossalivação não obteve ainda um consenso geral, pelo que são necessários mais estudos nesta área, para que ocorra a sua uniformização.The dry mouth sensation can have a subjective nature, called xerostomia, or it can be associated to salivary gland hypofunction (hyposalivation) or a change in the composition of saliva. Despite their indiscriminate use, these are two different concepts, which are often underrated and subdiagnosed by the dentist. Patients with salivary gland hypofunction are subject to various complications, such as dysgeusia, pain, a burning sensation in the oral mucosa, dental caries and other infectious diseases, dysphagia and dysphonia, which are common complaints in the dental medicine appointment. So far, there hasn’t been a general consensus over the treatment options for a patient with hyposalivation, therefore further research is necessary in order to achieve a uniformization.