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Journal articles on the topic 'In vivo et in vitro'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Phillips, Paddy A., John Risvanis, Kathryn Aldred, Louise M. Burrell, and Briony Bartholomeusz. "Differential Effects of a Novel Non-Peptide Endothelin Receptor Antagonist (Bosentan) in Rat Liver and Vasculature." Clinical Science 89, no. 6 (1995): 575–79. http://dx.doi.org/10.1042/cs0890575.

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1. We studied the effects of the non-selective, non-peptide, orally active endothelin (ET) receptor antagonist bosentan (Ro 47–0203) on rat hepatic and mesenteric vascular membrane 125I-ET-1 binding characteristics in vitro and ex vivo (after bosentan by gavage in vivo). 2. Bosentan caused a concentration-dependent competitive inhibition of 125I-ET-1 binding to female rat mesenteric vascular (predominantly ETA receptors) and hepatic (predominantly ETB receptors) membranes in vitro and ex viva 3. The time course of the inhibition of binding ex vivo after administration of bosentan in vivo was 1

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Jacqueline, C., J. Caillon, and G. Potel. "Linézolide, données récentes expérimentales in vitro et in vivo." Antibiotiques 7, no. 4 (2005): 225–33. http://dx.doi.org/10.1016/s1294-5501(05)80455-8.

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Wang, C., R. Zhao, B. Li, LY Gu, and H. Gou. "An in vivo and in vitro study." Human & Experimental Toxicology 35, no. 4 (2015): 404–17. http://dx.doi.org/10.1177/0960327115591374.

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Danshen injection, a pharmaceutical dosage form of Danshen, has been widely used in the treatment of coronary heart diseases, myocardial infarction, and hypertension. With more and more adverse drug reactions linked with Danshen injection, its safety comes under suspicion. To evaluate its safety, mice were divided into four groups: vehicle, low-, middle-, and high-Danshen group, and each group was intravenously administered with Danshen injection at a dose of 0, 0.64, 1.55, and 5.76 g/kg/day for 5 days, respectively (the low dosage was the recommended clinical dosage, the middle dosage was the

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4

Gouget, B., and J. Fonteneau. "Biocapteurs in vitro, ex vivo, in vivo et “point of care testing (POCT)”." Revue Française des Laboratoires 1997, no. 292 (1997): 73–76. http://dx.doi.org/10.1016/s0338-9898(97)80041-8.

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5

Acar, Niyazi, and Jean-Michel Lecerf. "Peroxydation in vivo et in vitro des acides gras polyinsaturés." Cahiers de Nutrition et de Diététique 42, no. 5 (2007): 260–65. http://dx.doi.org/10.1016/s0007-9960(07)73935-4.

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Godet, E., B. Vasseur, and M. Sabut. "Essais de génotoxicité in vitro et in vivo applicables à l'environnement hydrique." Revue des sciences de l'eau 6, no. 3 (2005): 285–314. http://dx.doi.org/10.7202/705177ar.

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Cet article est une revue des essais in vitro et in vivo utilisés pour évaluer le caractère génotoxique des micropolluants des milieux environnementaux relatifs aux eaux continentales et marines, rejets liquides d'origine domestique, industrielle ou agricole, sédiments de rivières et boues de stations de traitement d'épuration. Les essais in vitro réalisés sur cellules eucaryotes ou procaryotes sont fondés sur la détection des mutations géniques et chromosomiques, ou la mesure des adduits à l'ADN. Ils constituent des systèmes d'épreuve miniaturisés qui requièrent des volumes d'échantillons fai

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COGNIE, Y., and G. BARIL. "Le point sur la production et le transfert d’embryons obtenus in vivo et in vitro chez la brebis et la chèvre." INRAE Productions Animales 15, no. 3 (2002): 199–207. http://dx.doi.org/10.20870/productions-animales.2002.15.3.3701.

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Cet article décrit les bases des techniques de production in vivo et in vitro des embryons ovins et caprins. Malgré les améliorations apportées à la technique, les limites de la production d’embryons in vivo sont précisées : variabilité de la réponse au traitement hormonal, fécondation difficile des femelles fortement superovulées, importance de la régression prématurée des corps jaunes chez la chèvre. Les nouvelles perspectives offertes par les ponctions répétées des ovocytes chez une même femelle, suivies de la production des embryons in vitro, sont présentées avec leurs limites actuelles et

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Sano, Naoto, Takashi Shibamoto, Yutaka Yoshimoto, et al. "In vitro and in vivo assessments of anti-ET contamination couplers." Nihon Toseki Igakkai Zasshi 34, no. 4 (2001): 257–62. http://dx.doi.org/10.4009/jsdt.34.257.

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JARDIN, A., V. IZARD, G. BENOIT, et al. "Fécondance in vivo et in vitro de spermatozoïdes épididymaires humains immatures." Reproduction Nutrition Développement 28, no. 5 (1988): 1375–85. http://dx.doi.org/10.1051/rnd:19880818.

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10

Mallié, M., and S. Bertout. "Caspofungine et mycoses à champignons rares : activité in vitro et in vivo chez l’animal et chez l’homme." Journal de Mycologie Médicale 17, no. 1 (2007): 25–32. http://dx.doi.org/10.1016/j.mycmed.2006.12.006.

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11

Bande, Omprakash, Darren Braddick, Stefano Agnello, et al. "Correction: Base pairing involving artificial bases in vitro and in vivo." Chemical Science 7, no. 2 (2016): 1611. http://dx.doi.org/10.1039/c5sc90070k.

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12

Wood, C. D., A. H. Murray, A. R. Moss, and D. I. Givens. "Use of the gas production technique to investigate responses of supplementing low quality forages. 1. In vitro interactions." BSAP Occasional Publication 22 (1998): 92–94. http://dx.doi.org/10.1017/s0263967x0003233x.

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Nitrogen-deficient fibrous crop residues are widely used as basal diets in less developed countries, particularly in dry seasons when alternative foods are often in short supply. One approach to improving animal performance on crop residue based diets is to include a supplement of improved quality food to provide fermentable protein and energy. There are no established in vitro methods for investigating interactions between foods but the in vitro gas production method shows promise in this regard (Prasad et al., 1994). This paper describes the interactions observed in vitro; an accompanying pa

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Bonamin, Leoni V. "Homéopathie et infections expérimentales : expérimentations in vivo et in vitro sur des bactéries, des champignons et des protozoaires." La Revue d'Homéopathie 10, no. 4 (2019): 155–58. http://dx.doi.org/10.1016/j.revhom.2019.10.019.

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14

Sansonetti, Philippe. "« Voir c’est croire» : imagerie in vitro et in vivo des processus infectieux." La lettre du Collège de France, no. 26 (June 1, 2009): 27–28. http://dx.doi.org/10.4000/lettre-cdf.144.

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15

Bonnet, J. J., H. Legros, Fr Janin, N. Dourmap, and J. Costentin. "Recherche d’une toxicité du 3,4-dihydroxyphénylacétaldéhyde (DOPAL) in vitro et in vivo." Annales Pharmaceutiques Françaises 62, no. 5 (2004): 323–31. http://dx.doi.org/10.1016/s0003-4509(04)94321-0.

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Mouchard, F., A. C. De Boigrollier, P. Vera, and P. Bohn. "Étude in vitro et in vivo d’un nouveau traceur TEMP de l’apoptose." Médecine Nucléaire 37, no. 5 (2013): 172. http://dx.doi.org/10.1016/j.mednuc.2013.03.142.

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17

Drugeon, H. B., and R. Garraffo. "Pharmacocinétique et pouvoir bactéricide du céfuroxime axétil : modèle in vitro/ex vivo." Médecine et Maladies Infectieuses 21 (September 1991): 56–60. http://dx.doi.org/10.1016/s0399-077x(05)80475-5.

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Aloulou, I., R. Bousoffara, M. Ben Khalifa, et al. "Évaluation in vitro et in vivo d’une chambre d’inhalation fabriquée en Tunisie." Revue Française d'Allergologie et d'Immunologie Clinique 41, no. 6 (2001): 537–43. http://dx.doi.org/10.1016/s0335-7457(01)00069-7.

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19

Bigliani, V., and L. S. Pilowsky. "In vivo neuropharmacology of schizophrenia." British Journal of Psychiatry 174, S38 (1999): 23–33. http://dx.doi.org/10.1192/s0007125000298085.

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Since the introduction of chlorpromazine in the 1950s, followed by the discovery (with in vitro receptor binding assays), in the mid-1970s, that antipsychotic drugs block a subtype of dopamine receptor (D2/D2-like) (Creese et al, 1976) and that affinity for these receptors appears to correlate directly with clinical potency for antipsychotics (Peroutka & Synder, 1980), the study of neurotransmitters and receptors has been a major target of schizophrenia research (Owens, 1996). In 1983, the first visualisation, by positron emission tomography (PET), of the binding of D2 dopamine receptors i

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PICARD-HAGEN, N., V. GAYRARD, C. VIGUIE, V. LAROUTE, and P. ALAYRAC. "Absence d’efficacité de la quinacrine dans le traitement des maladies à prions : possible explication à caractère pharmacologique." INRAE Productions Animales 17, HS (2020): 101–8. http://dx.doi.org/10.20870/productions-animales.2004.17.hs.3634.

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En raison des incertitudes épidémiologiques relatives aux maladies à prions, il est urgent de découvrir et de développer des thérapeutiques anti-prions chez l’homme. L’efficacité des molécules candidates est essentiellement testée in vitro sur des cellules de neuroblastome. Pour plusieurs molécules, dont la quinacrine, il a été observé une discordance entre l’effet anti-prion in vitro et l’absence d’efficacité clinique dans le traitement de la maladie de Creutzfeldt-Jakob. Pour documenter l’hypothèse selon laquelle l’absence d’efficacité de la quinacrine était d’ordre pharmacocinétique (et don

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Chamkhi, A., O. Seloi, A. Heintz, et al. "Glioblastomes : spectroscopie in vivo et anatomopathologie in vitro pour le pronostic et le suivi du traitement." Journal of Neuroradiology 44, no. 2 (2017): 99. http://dx.doi.org/10.1016/j.neurad.2017.01.061.

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Yu, Jing, Hui Ye, Jiang Li, Ning Li, Zong-ming Shi, and Xue-zhi Zhang. "The Antibacterial Activity of Mass Galla Chinesis et Camelliae Fermentata on Helicobacter pylori Infection." Evidence-Based Complementary and Alternative Medicine 2018 (2018): 1–6. http://dx.doi.org/10.1155/2018/1491732.

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Mass Galla chinesis et camelliae Fermentata (Chinese gall leaven, CGL) was investigated for activities against Helicobacter pylori (H. pylori) both in vitro and in vivo. The agar dilution method and time-kill curves, as in vitro assays and an in vivo study using a Kunming mice model, were performed. CGL demonstrated a strong anti-Helicobacter pylori activity in vitro with the minimal inhibitory concentrations (MICs) against multiple H. pylori strains of 0.5~8 mg/ml and the decreasing trend time-kill curves when increasing CGL concentrations. H. pylori eradication rates in vivo were evaluated b

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Kang, Bum-Yong, Jennifer M. Kleinhenz, Tamara C. Murphy та C. Michael Hart. "The PPARγ ligand rosiglitazone attenuates hypoxia-induced endothelin signaling in vitro and in vivo". American Journal of Physiology-Lung Cellular and Molecular Physiology 301, № 6 (2011): L881—L891. http://dx.doi.org/10.1152/ajplung.00195.2011.

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Peroxisome proliferator-activated receptor (PPAR) γ activation attenuates hypoxia-induced pulmonary hypertension (PH) in mice. The current study examined the hypothesis that PPARγ attenuates hypoxia-induced endothelin-1 (ET-1) signaling to mediate these therapeutic effects. To test this hypothesis, human pulmonary artery endothelial cells (HPAECs) were exposed to normoxia or hypoxia (1% O2) for 72 h and treated with or without the PPARγ ligand rosiglitazone (RSG, 10 μM) during the final 24 h of exposure. HPAEC proliferation was measured with MTT assays or cell counting, and mRNA and protein le

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Dieguez, G., J. L. Garcia, N. Fernandez, A. L. Garcia-Villalon, L. Monge, and B. Gomez. "Cerebrovascular and coronary effects of endothelin-1 in the goat." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 263, no. 4 (1992): R834—R839. http://dx.doi.org/10.1152/ajpregu.1992.263.4.r834.

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In vivo and in vitro effects of endothelin-1 (ET-1) on cerebral and coronary vasculature of goats were examined and compared. In six anesthetized goats intravenous injections of ET-1 (0.1-0.8 nmol) increased arterial pressure, did not change the middle cerebral (MCA) and left anterior descending or left circumflex coronary (LCC) arterial blood flows (electromagnetically measured), and increased cerebral and coronary vascular resistances. In four other anesthetized goats intra-arterial injections of ET-1 (0.01-0.3 nmol) decreased the MCA flow less than the LCC flow (maximal reduction was 20 and

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Richard, C., S. Degrelle, V. Gelin, et al. "85 Elongation of trophoblastic vesicles between Days 15 and 18 in cattle." Reproduction, Fertility and Development 31, no. 1 (2019): 168. http://dx.doi.org/10.1071/rdv31n1ab85.

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Once formed, bovine blastocysts differentiate while growing exponentially from 150-200μm (Days 7 or 8) to 200-250mm (Days 17 to 18; Sandra et al. 2017 Annu. Rev. Anim. Biosci. 5, 205-228). Thus, the length of the conceptus doubles every day between Days 9 and 16 (Berg et al. 2010 Theriogenology 73, 250-260); however, this was observed on whole conceptuses. The objective of the current study was to test whether this elongation rate is similar when the embryonic disc has been excised. Six heifers were used to produce Day-15 conceptuses, either fully developed in vivo or developed in vivo for a w

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Chambers, A. F., and S. Wilson. "Cells transformed with a ts viral src mutant are temperature sensitive for in vivo growth." Molecular and Cellular Biology 5, no. 4 (1985): 728–33. http://dx.doi.org/10.1128/mcb.5.4.728.

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Studies on ts mutants of avian sarcoma viruses have previously implicated the src gene product (pp60src) kinase function in in vitro transformation. The role of src in vivo, however, has not been clearly defined. Using a sensitive and quantitative assay that was developed in chicken embryos (Chambers et al., Cancer Res. 42:4018-4025, 1982), we tested the in vivo tumorigenic properties of cells transformed with LA23, an avian sarcoma virus that is temperature sensitive for in vitro transformation. We found that the in vivo growth ability of these cells was temperature sensitive and that this in

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Chambers, A. F., and S. Wilson. "Cells transformed with a ts viral src mutant are temperature sensitive for in vivo growth." Molecular and Cellular Biology 5, no. 4 (1985): 728–33. http://dx.doi.org/10.1128/mcb.5.4.728-733.1985.

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Studies on ts mutants of avian sarcoma viruses have previously implicated the src gene product (pp60src) kinase function in in vitro transformation. The role of src in vivo, however, has not been clearly defined. Using a sensitive and quantitative assay that was developed in chicken embryos (Chambers et al., Cancer Res. 42:4018-4025, 1982), we tested the in vivo tumorigenic properties of cells transformed with LA23, an avian sarcoma virus that is temperature sensitive for in vitro transformation. We found that the in vivo growth ability of these cells was temperature sensitive and that this in

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Muelling, Christoph KW, Ulrike Nebel, and Rya-Yvonne Wuestenberg. "Innovative in vitro and ex vivo models for studying bovine hoof biology." Proceedings of the British Society of Animal Science 2007 (April 2007): 266. http://dx.doi.org/10.1017/s1752756200021694.

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Research into the biology and physiopathology of the bovine claw has become interdisciplinary employing epidemiology, cellular and molecular biology. Foot disorders in cattle are a global problem causing substantial economic losses to farmers. New hypotheses demonstrate possible links between systemic problems and local damage in the claw. Tissue explant and cell culture studies have already provided important insights into regulation of differentiation in healthy and diseased claw tissue (Hendry et al 1997, 2003; Nebel et al 2002, 2004). Detailed knowledge of the links between systemic events

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Attrassi, Khaled, Rachid Benkirane, Benaissa Attrassi, and Allal Douira. "Effet de l’association de certains fongicides avec le chlorure de calcium sur le développement d’un complexe fongique responsable de la pourriture des pommes en conservation." Phytoprotection 88, no. 1 (2007): 17–26. http://dx.doi.org/10.7202/016398ar.

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L’utilisation du bénomyl et du thiabendazole (famille chimique des benzimidazoles), de l’azoxystrobine et du pyriméthanil montre, autant in vitro qu’in vivo, que ces fongicides sont faiblement à moyennement efficaces contre les agents pathogènes suivants : Rhizopus stolonifer, Penicillium expansum, Aspergillus niger, A. fumigatus, Alternaria alternata, Cladosporium herbarum, Fusarium oxysporum, Saccharomyces cerevisiae, Monilia fructigina, Cryptosporiopsis malicorticis, Spilocaea pomi et Trichothecium roseum. Utilisé in vitro, le chlorure de calcium seul à plus de 4 % est toléré par les douze

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CORPET, D. E. "Etude de l'écologie microbienne de l'intestin : modèles in vitro, in vivo et mathématiques." Revue Scientifique et Technique de l'OIE 8, no. 2 (1989): 375–89. http://dx.doi.org/10.20506/rst.8.2.407.

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Betis, F., N. Cuburu, P. Gastaud, and P. Hofman. "La chlorhexidine induit in vivo et in vitro une nécrose des cellules épithéliales." Annales de Pathologie 24 (November 2004): 136. http://dx.doi.org/10.1016/s0242-6498(04)94126-0.

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Sapet, Cédric, Nicolas Laurent, Loïc Le Gourrierec, Séverine Augier, and Olivier Zelphati. "Magnétofection™ in vitro et in vivo: une voie vers la thérapie génique." Annales de biologie clinique 68, no. 2 (2010): 133–42. http://dx.doi.org/10.1684/abc.2010.0417.

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Kelly, J., D. Kleemann, M. Kuwayama, and S. Walker. "88 PREGNANCY RATES FOR IN VITRO AND IN VIVO PRODUCED OVINE EMBRYOS VITRIFIED USING THE MINIMUM VOLUME COOLING CRYOTOP METHOD." Reproduction, Fertility and Development 17, no. 2 (2005): 194. http://dx.doi.org/10.1071/rdv17n2ab88.

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Previously we reported that, using the minimum volume cooling (MVC) cryotop vitrification method, in vitro-produced ovine and bovine embryo survival after thawing was similiar to that of fresh embryos (Kelly et al. 2004 Reprod. Fert. Dev. 16, 172). While survival of vitrified embryos after thawing can be indicative of embryo viability, this assessment does not always correlate with embryo survival after transfer. This study assesses the effect of vitrification using the MVC cryotop method on the survival after transfer of in vitro- and in vivo-produced ovine embryos. Fresh or vitrified Day 6 o

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Hussain, A., and E. L. Miller. "Effect of feeding lactose on rumen metabolism in-vitro and in-vivo." Proceedings of the British Society of Animal Science 1998 (1998): 168. http://dx.doi.org/10.1017/s030822960003381x.

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Inclusion of lactose in dairy cow rations increases dry matter intake (DMI) and milk yield (Garnsworthy 1996). This may be due to the relatively slow rate of lactose fermentation ( Hussain and Miller, 1998) sustaining better regulation of rumen pH and also possible consequence for microbial protein synthesis (Chamberlain et al., 1993).This experiment was conducted to study the changes in rumen environment over the adaptation period and effect of these changes on the fermentation of lactose itself.Three Suffolk wethers (b.wt 56± 7.36 kg) maintained on hay and concentrate (600:400) were offered

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Shelley, Michael L., Andrew J. Wagner, Saber M. Hussain, and Charles Bleckmann. "Modeling the In Vivo Case with In Vitro Nanotoxicity Data." International Journal of Toxicology 27, no. 5 (2008): 359–67. http://dx.doi.org/10.1080/10915810802503487.

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As more in vitro nanotoxicity data appear in the literature, these findings must be translated to in vivo effects to define nanoparticle exposure risk. Physiologically based pharmacokinetic (PBPK) modeling has played a significant role in guiding and validating in vivo studies for molecular chemical exposure and can develop as a significant tool in guiding similar nanotoxicity studies. This study models the population dynamics of a single cell type within a specific tissue. It is the first attempt to model the in vitro effects of a nanoparticle exposure, in this case aluminum (80 nm) and its i

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Pan, Chenhao, Lei Chen, Ruoyu Wu, et al. "Correction: Lithium-containing biomaterials inhibit osteoclastogenesis of macrophages in vitro and osteolysis in vivo." Journal of Materials Chemistry B 7, no. 15 (2019): 2566. http://dx.doi.org/10.1039/c9tb90039j.

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Frers, L., J. Hepburn, J. Mandriaza Munoz, J. Forsyth, and K. Strongman. "63 VITRIFICATION OF BOVINE IN VITRO-PRODUCED AND IN VIVO EMBRYOS." Reproduction, Fertility and Development 21, no. 1 (2009): 131. http://dx.doi.org/10.1071/rdv21n1ab63.

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There is increasing interest in vitrification as a method of cryopreserving bovine embryos, especially previously problematic embryos such as IVP and Jersey cattle embryos, which, it has been suggested, have lower tolerance to cryopreservation because of the high lipid content of the embryo interfering with water movement out of the cells. Jersey embryos were demonstrated to have lower pregnancy rates following cryopreservation compared with Holstein embryos [Steel R et al. 2004 Reprod. Fertil. Dev. 16(Suppl. 2), 120 abst]. The first trial aimed to compare the subsequent pregnancy rate of vitr

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Teferedegne, B., P. O. Osuji, A. Odenyo, R. J. Wallace, and C. J. Newbold. "Influence of saponins and sapogenins on the bacteriolytic activity of ciliate protozoa from the sheep rumen." Proceedings of the British Society of Animal Science 1998 (1998): 88. http://dx.doi.org/10.1017/s0308229600033018.

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Foliage from the tropical leguminous tree, Sesbania sesban, is toxic to rumen protozoa in vitro, due to materials present in a saponins-containing extract of the foliage (Newbold et al. 1997). Suppression of protozoal numbers in vivo when S. sesban is added to the diet is either transient or non-existent, however, even though washed protozoa remain sensitive to S. sesban in vitro (Newbold et al. 1997, Odenyo et al. 1997). A possible reason is that saponins are metabolised in rumen fluid (Makkar and Becker 1997). The aims of this study were to determine if the antiprotozoal effect of different

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Rigel, D. F., and S. S. Shetty. "A novel model of conduit coronary constriction reveals local actions of endothelin-1 and prostaglandin F2alpha." American Journal of Physiology-Heart and Circulatory Physiology 272, no. 4 (1997): H2054—H2064. http://dx.doi.org/10.1152/ajpheart.1997.272.4.h2054.

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We evaluated the effects of endothelin-1 (ET-1) and prostaglandin F2alpha (PGF2alpha) selectively on conduit coronary artery diameter using a novel approach in which the local concentration of vasoactive agent was controlled and maintained in vivo. ET-1 and PGF2alpha were applied topically (100 microl every 3 min) to the external surface of the left circumflex coronary artery (LCx) in anesthetized dogs or to the bathing medium of isolated canine LCx rings in parallel in vitro experiments. The dose-dependent constrictions obtained in vivo and in vitro were similar with each agent. Single, appro

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Newland, N. L., P. J. S. Smith, and E. A. Howes. "REGENERATING ADULT COCKROACH DORSAL UNPAIRED MEDIAN NEURONES IN VITRO RETAIN THEIR IN VIVO MEMBRANE CHARACTERISTICS." Journal of Experimental Biology 179, no. 1 (1993): 323–29. http://dx.doi.org/10.1242/jeb.179.1.323.

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The ability of differentiated neurones to recover from disease or injury depends upon both intrinsic and extrinsic factors. Whereas most mammalian neurones have a limited capacity for regeneration, regulated, in part, by physical and chemical cues in the brain microenvironment (Bray et al. 1987; Caroni and Schwab, 1988, 1989), invertebrates, and in particular insects, exhibit a far greater capacity for repair of central neurones and circuits (Treherne et al. 1988). Studies of the cues that regulate the regenerative process are made easier by the use of individual, identified neurones, cultured

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Nankervis, Craig A., and Philip T. Nowicki. "Role of endothelin-1 in regulation of the postnatal intestinal circulation." American Journal of Physiology-Gastrointestinal and Liver Physiology 278, no. 3 (2000): G367—G375. http://dx.doi.org/10.1152/ajpgi.2000.278.3.g367.

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Newborn intestine is uniquely prone to vasoconstriction in response to a wide variety of perturbations. To test the hypothesis that endothelin (ET)-1 is an important factor in this process, we determined the effects of exogenous ET-1 administration and blockade of endogenous ET-1 in vivo and in vitro in 3- and 35-day-old swine. Intramesenteric artery administration of exogenous ET-1 to vascularly isolated in vivo gut loops (10−9 M/kg bolus) caused vasoconstriction and reduced gut O2 uptake similarly in these age groups. Selective blockade of ETA or ETB receptors with BQ-610 or BQ-788, respecti

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Dean, R., J. Zhuo, D. Alcorn, D. Casley, and F. A. Mendelsohn. "Cellular distribution of 125I-endothelin-1 binding in rat kidney following in vivo labeling." American Journal of Physiology-Renal Physiology 267, no. 5 (1994): F845—F852. http://dx.doi.org/10.1152/ajprenal.1994.267.5.f845.

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Endothelin-1 (ET-1) receptors have previously been demonstrated in the rat kidney by in vitro autoradiography and in cultured renal cell lines by radioreceptor assay, but the precise cellular localization of these receptors under in vivo conditions remains to be determined. We performed electron microscopic autoradiography on rat kidney following intravenous administration of 125I-labeled ET-1. In vivo autoradiographs revealed binding patterns identical to those previously demonstrated following in vitro labeling. Light microscopic autoradiography showed that silver grains occurred exclusively

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43

Montaudon, M., P. Caix, and F. Laurent. "Évaluation des surfaces de paroi et de lumière bronchiques par tomodensitométrie quantitative: validation in vitro et in vivo." Morphologie 91, no. 293 (2007): 94. http://dx.doi.org/10.1016/j.morpho.2007.09.029.

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44

Boyer, G., S. Brédif, G. Bellemère, A. Moga, C. de Belilovsky, and C. Baudouin. "Caractérisation de la peau sèche du nouveau-né et de l’enfant par approches in vitro et in vivo." Annales de Dermatologie et de Vénéréologie 143, no. 12 (2016): S303—S304. http://dx.doi.org/10.1016/j.annder.2016.09.455.

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Mertens, E., U. Besenfelder, M. Gilles, et al. "190 INFLUENCE OF IN VITRO CULTURE OF BOVINE EMBRYOS ON THE STRUCTURE OF THE ZONA PELLUCIDA." Reproduction, Fertility and Development 19, no. 1 (2007): 211. http://dx.doi.org/10.1071/rdv19n1ab190.

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The zona pellucida is an extracellular structure at the direct interface between the maternal and embryonic sides, through which all signals of the embryo–maternal dialogue as well as nutritional factors have to pass. Up to now there has been no investigation as to whether in vitro culture influences the structure of the zona pellucida compared to that of in vivo embryos. Therefore, in vitro (oocyte, zygote, 2-, 4-, 8-, 16-cell, morula, and Day 7 blastocyst, using the protocol published by Nganvongpanit et al. 2006 Reproduction 131, 861–874) and in vivo (zygote, 4-cell, morula, and blastocyst)

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FONTAINE, Emmanuel, Karine REYNAUD, Sandra THOUMIRE, et al. "MICROENVIRONNEMENT TUBAIRE: RÔLE DANS LA MATURATION DES OVOCYTES CANINS IN VIVO ET IN VITRO." Bulletin de l'Académie vétérinaire de France, no. 1 (2009): 145. http://dx.doi.org/10.4267/2042/47987.

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Pagniez, F., R. Guillon, C. Picot, F. Morio, C. Loge, and P. Le Pape. "Activité in vitro et in vivo de nouveaux dérives de l’albaconazole sur Candida spp." Journal de Mycologie Médicale 22, no. 1 (2012): 119. http://dx.doi.org/10.1016/j.mycmed.2011.12.062.

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Lavallard, V., S. Bonnafous, A. Bertola, et al. "P220 Étude de l’autophagie dans la mort cellulaire hépatocytaire in vitro et in vivo." Diabetes & Metabolism 35 (March 2009): A79. http://dx.doi.org/10.1016/s1262-3636(09)72018-x.

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Ghelardini, Carla, Alessandro Bartolini, Nicoletta Galeotti, Elisabetta Teodori, and Fulvio Gualtieri. "S-(−)-ET 126: A potent and selectivE M1 antagonist in vitro and in vivo." Life Sciences 58, no. 12 (1996): 991–1000. http://dx.doi.org/10.1016/0024-3205(96)00047-1.

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Jang, Ji-Hye, Chang-Seob Seo, Hyekyung Ha, Su-Cheol Han, Mee-Young Lee, and Hyeun-Kyoo Shin. "Genotoxicity of Asiasari Radix et Rhizoma (Aristolochiaceae) ethanolic extract in vitro and in vivo." Journal of Ethnopharmacology 276 (August 2021): 114122. http://dx.doi.org/10.1016/j.jep.2021.114122.

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