Bibliografías temáticas / Bradykinin B2

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Literatura académica sobre el tema "Bradykinin B2"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 8 de febrero de 2022

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Artículos de revistas sobre el tema "Bradykinin B2"

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Ma, Jie, Yu Luo, Lilin Ge, et al. "Ranakinestatin-PPF from the Skin Secretion of the Fukien Gold-Striped Pond Frog,Pelophylax plancyi fukienensis: A Prototype of a Novel Class of BradykininB2Receptor Antagonist Peptide from Ranid Frogs." Scientific World Journal 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/564839.

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The defensive skin secretions of many amphibians are a rich source of bradykinins and bradykinin-related peptides (BRPs). Members of this peptide group are also common components of reptile and arthropod venoms due to their multiple biological functions that include induction of pain, effects on many smooth muscle types, and lowering systemic blood pressure. While most BRPs are bradykinin receptor agonists, some have curiously been found to be exquisite antagonists, such as the maximakinin gene-related peptide, kinestatin—a specific bradykinin B2-receptor antagonist from the skin of the giant
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Dixon, B. S., R. Breckon, J. Fortune, et al. "Effects of kinins on cultured arterial smooth muscle." American Journal of Physiology-Cell Physiology 258, no. 2 (1990): C299—C308. http://dx.doi.org/10.1152/ajpcell.1990.258.2.c299.

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The present study uses various kinin agonists and antagonists to examine the cellular mechanisms of bradykinin's actions on intracellular calcium, prostaglandins, and adenosine 3',5'-cyclic monophosphate (cAMP) accumulation in cultured arterial smooth muscle cells (casmc) obtained from rat mesenteric arteries. Exposure to bradykinin produced a rapid release of calcium (peak less than or equal to 20 s) from intracellular stores and an increase in prostaglandin (PG) E2 and cAMP production in casmc. Compared with bradykinin, the bradykinin B1-agonist [des-Arg9]BK produced only a small increase in
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3

Willars, Gary B., Werner Müller-Esterl, and Stefan R. Nahorski. "Receptor phosphorylation does not mediate cross talk between muscarinic M3 and bradykinin B2 receptors." American Journal of Physiology-Cell Physiology 277, no. 5 (1999): C859—C869. http://dx.doi.org/10.1152/ajpcell.1999.277.5.c859.

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This study examined cross talk between phospholipase C-coupled muscarinic M3 and bradykinin B2 receptors coexpressed in Chinese hamster ovary (CHO) cells. Agonists of either receptor enhanced phosphoinositide signaling (which rapidly desensitized) and caused protein kinase C (PKC)-independent, homologous receptor phosphorylation. Muscarinic M3 but not bradykinin B2 receptors were also phosphorylated after phorbol ester activation of PKC. Consistent with this, muscarinic M3 receptors were phosphorylated in a PKC-dependent fashion after bradykinin B2 receptor activation, but muscarinic M3 recept
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Regoli, D. "Multiple bradykinin B2 receptors." Trends in Pharmacological Sciences 10, no. 4 (1989): 138. http://dx.doi.org/10.1016/0165-6147(89)90163-6.

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Pan, H. L., C. L. Stebbins, and J. C. Longhurst. "Bradykinin contributes to the exercise pressor reflex: mechanism of action." Journal of Applied Physiology 75, no. 5 (1993): 2061–68. http://dx.doi.org/10.1152/jappl.1993.75.5.2061.

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This study determined the receptors responsible for mediating bradykinin's effect on skeletal muscle afferents that cause the pressor reflex in anesthetized cats. In eight cats, 1 microgram of bradykinin was injected intra-arterially into the gracilis muscle before and after intravenous injection of a kinin B2-receptor antagonist (NPC 17731, 20 micrograms/kg). Initial injection of bradykinin reflexly increased mean arterial pressure by 23 +/- 7 mmHg, maximal change in pressure over time by 439 +/- 272 mmHg/s, and heart rate by 11 +/- 4 beats/min. The hemodynamic response to bradykinin was abol
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6

Schanstra, Joost P., Johan Duchene, Françoise Praddaude, et al. "Decreased renal NO excretion and reduced glomerular tuft area in mice lacking the bradykinin B2 receptor." American Journal of Physiology-Heart and Circulatory Physiology 284, no. 6 (2003): H1904—H1908. http://dx.doi.org/10.1152/ajpheart.01150.2002.

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Bradykinin B2 receptor knockout mice (B2 −/−) have been useful to study the role of bradykinin under pathological conditions. With the use of these mice, it was shown that bradykinin plays an important role in angiogenesis, heart failure, salt-induced hypertension, and kidney fibrosis. Data on the role of the bradykinin B2 receptor under physiological conditions using these mice are controversial and scarce, because these mice have no typical phenotype. For this reason, we have studied, under physiological conditions, renal hemodynamics as well as a number of morphometric glomerular parameters
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Stewart, John M. "Bradykinin B2 receptor antagonists: development and applications." Canadian Journal of Physiology and Pharmacology 73, no. 7 (1995): 787–90. http://dx.doi.org/10.1139/y95-106.

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Most physiological and pathophysiological responses to bradykinin are mediated by G-protein-coupled receptors designated B2 receptors. Discovery of antagonists for these receptors has brought about a revolution in research in the kinin field. The chemistry and development of antagonists for B2 kinin receptors are discussed. Uses of the antagonists in biomedical research and potential clinical applications are presented.Key words: bradykinin antagonists, bradykinin inflammation, bradykinin receptors.
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Gröger, Moritz, Diane Lebesgue, Didier Pruneau, et al. "Release of Bradykinin and Expression of Kinin B2 Receptors in the Brain: Role for Cell Death and Brain Edema Formation After Focal Cerebral Ischemia in Mice." Journal of Cerebral Blood Flow & Metabolism 25, no. 8 (2005): 978–89. http://dx.doi.org/10.1038/sj.jcbfm.9600096.

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Pharmacological studies using bradykinin B2 receptor antagonists suggest that bradykinin, an early mediator of inflammation and the main metabolite of the kallikrein-kinin system, is involved in secondary brain damage after cerebral ischemia. However, the time-course of bradykinin production and kinin receptor expression as well as the conclusive role of bradykinin B2 receptors for brain damage after experimental stroke have not been elucidated so far. C57/Bl6 mice were subjected to 45 mins of middle cerebral artery occlusion (MCAO) and 2, 4, 8, 24, and 48 h later brains were removed for the a
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9

Hess, J. Fred, Patricia J. Hey, Tsing-Bau Chen, et al. "Molecular Cloning and Pharmacological Characterization of the Canine B1 and B2 Bradykinin Receptors." Biological Chemistry 382, no. 1 (2001): 123–29. http://dx.doi.org/10.1515/bc.2001.018.

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Abstract The dog is a valuable animal model in the study of the physiological role of both the B1 and B2 bradykinin receptors. To more thoroughly characterize the pharmacological properties of the canine kinin receptors we isolated the cDNA sequence encoding the B1 and B2 bradykinin receptor subtypes and overexpressed them in Chinese hamster ovary (CHO) cells. The cDNA sequence of the canine B1 bradykinin receptor encodes a protein comprised of 350 amino acids that is 76% identical to the human B1 bradykinin receptor. The cDNA sequence of the canine B2 bradykinin receptor encodes a protein of
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10

Xiao, Hong D., Sebastien Fuchs, Justin M. Cole, Kevin M. Disher, Roy L. Sutliff, and Kenneth E. Bernstein. "Role of bradykinin in angiotensin-converting enzyme knockout mice." American Journal of Physiology-Heart and Circulatory Physiology 284, no. 6 (2003): H1969—H1977. http://dx.doi.org/10.1152/ajpheart.00010.2003.

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Angiotensin-converting enzyme (ACE) plays a central role in the renin-angiotensin system. Whereas ACE is responsible for the production of angiotensin II, it is also important in the elimination of bradykinin. Constitutively, the biological function of bradykinin is mediated through the bradykinin B2 receptor. ACE knockout mice have a complicated phenotype including very low blood pressure. To investigate the role of bradykinin in the expression of the ACE knockout phenotype, we bred B2 receptor knockout mice with ACE knockout mice, thus generating a line of mice deficient in both the B2 recep
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Tesis sobre el tema "Bradykinin B2"

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Willer, Elizabeth Jane. "Control of B2 bradykinin receptor gene expression." Thesis, University College London (University of London), 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286487.

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Holz, Alexander. "Theoretische Untersuchungen zum Bindungsmodus nichtpeptidischer Bradykinin B2 Rezeptorantagonisten." [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968529038.

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Malmberg, Michelle. "Funktionella och farmakologiskakonsekvenser av Bradykinin B1-och B2-receptor samuttryck." Thesis, Umeå universitet, Kemiska institutionen, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-101863.

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4

UENO, Tomoyuki, Yasuko KOZAKI, and Kazue MIZUMURA. "Increased Expression of mRNA for B1 and B2 Bradykinin Receptors in the Skin of Adjuvant Inoculated Rats." Research Institute of Environmental Medicine, Nagoya University, 2002. http://hdl.handle.net/2237/2787.

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Said, Najeeb Barrah. "The design and synthesis of non-peptide bradykinin B2 receptor antagonists." Thesis, University College London (University of London), 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285827.

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Feierler, Jens. "Die Funktion der Helix 8 für die Regulation des Bradykinin B2 Rezeptors." Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-143470.

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Schulz, Joachim. "Die therapeutische Wirkung eines neuen Bradykinin B2- Rezeptorantagonisten - LF160687 MS - auf das vasogene Hirnödem." Diss., lmu, 2005. http://nbn-resolving.de/urn:nbn:de:bvb:19-44107.

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8

Kläsner, Benjamin. "Antagonisierung von Bradykinin-B2-Rezeptoren nach fokaler zerebraler Ischämie - Therapeutisches Fenster bei der Ratte." Diss., lmu, 2006. http://nbn-resolving.de/urn:nbn:de:bvb:19-61084.

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Schwartz, Eike-Christian. "Expression und Lokalisation zentraler Bradykinin-B2-Rezeptoren Beteiligung an der Pathogenese von spontan hypertensiven Ratten? /." [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=975693395.

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Welte, Benjamin. "Rolle der Rezeptorkinasen GRK-2 und GRK-3 für die Regulation des humanen B2 Bradykinin Rezeptors." Diss., Ludwig-Maximilians-Universität München, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-157004.

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Capítulos de libros sobre el tema "Bradykinin B2"

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Yokoyama, S., H. Takeda, and H. Higashida. "B2 Bradykinin Receptors in Neuronal Cells: a Genetic Aspect." In Slow Synaptic Responses and Modulation. Springer Japan, 2000. http://dx.doi.org/10.1007/978-4-431-66973-9_50.

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2

Freedman, Richard, and Kurt Jarnagin. "Cloning of a B2 Bradykinin Receptor: Examination of the Bradykinin Binding Site by Site Directed Mutagenesis." In Recent Progress on Kinins. Birkhäuser Basel, 1992. http://dx.doi.org/10.1007/978-3-0348-7321-5_61.

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Turcani, Marian, and Heinz Rupp. "Bradykinin (B2) independent effect of captopril on the development of pressure overload cardiac hypertrophy." In Control of Gene Expression by Catecholamines and the Renin-Angiotensin System. Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4351-0_25.

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Novotny, E. A., M. A. Connolly, S. Chakravarty, et al. "Cloning of a human B2 bradykinin receptor: Functional expression and pharmacological characterization in Xenopus oocytes and mammalian cell lines." In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_143.

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Schulz, J., Nikolaus Plesnila, J. Eriskat, M. Stoffel, D. Pruneau, and A. Baethmann. "LF16-0687 A Novel Non-Peptide Bradykinin B2 Receptor Antagonist Reduces Vasogenic Brain Edema from a Focal Lesion in Rats." In Brain Edema XI. Springer Vienna, 2000. http://dx.doi.org/10.1007/978-3-7091-6346-7_28.

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6

Lehmberg, J., J. Beck, A. Baethmann, and Eberhard Uhl. "Influence of the Bradykinin Bl/B2-Receptor-Antagonist B 9430 on the Cerebral Microcirculation and Outcome of Gerbils from Global Cerebral Ischemia." In Brain Edema XI. Springer Vienna, 2000. http://dx.doi.org/10.1007/978-3-7091-6346-7_8.

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7

Zausinger, Stefan, D. B. Lumenta, D. Pruneau, R. Schmid-Elsaesser, N. Plesnila, and A. Baethmann. "Therapeutical efficacy of a novel non-peptide bradykinin B2 receptor antagonist on brain edema formation and ischemic tissue damage in focal cerebral ischemia." In Brain Edema XII. Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-0651-8_44.

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Müller-Esterl, Werner. "Immunological Probes for the Bradykinin B2 Receptor. A Toolbox." In The Kinin System. Elsevier, 1997. http://dx.doi.org/10.1016/b978-012249340-9/50008-5.

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Dziadulewicz, Edward K. "Bradykinin B2 Receptor Antagonists for the Treatment of Pain." In Annual Reports in Medicinal Chemistry. Elsevier, 2004. http://dx.doi.org/10.1016/s0065-7743(04)39009-3.

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Higashida, Haruhiro, Minako Hashii, Shigeru Yokoyama, et al. "Chapter 13. Bradykinin B2 receptors and signal transduction analyzed in NG108-15 neuroblastoma X glioma hybrid cells, B2 receptor-transformed CHO cells and ras-transformed NIH/3T3 fibroblasts." In Progress in Brain Research. Elsevier, 1996. http://dx.doi.org/10.1016/s0079-6123(08)61090-0.

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Actas de conferencias sobre el tema "Bradykinin B2"

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Yu, Hsin-Shan, and Chih-Hsin Tang. "Abstract 1396: Bradykinin enhances cell migration in human prostate carcinoma cells via bradykinin B2 receptor, PKCdelta, c-Src and NF-kappaB signaling pathways." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-1396.

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2

Egberg, Nils, Krister Gréen, Jan Jacobsson, Ole Vester-gvist, Bjöm Wiman, and Michael Gallimore. "EFFECTS OF PLASMA KALLIKREIN AND BRADYKININ ON FIBRINOLYSIS AND THROMBOXANE PROSTACYKLIN FORMATION STUDIED IN MINIPIGS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644334.

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The effect of plasma kallikrein and bradykinin infusions into pigs on hemodynamic and hemostatic variables have been investigated. Both substances caused a pronounced decrease of the systemic blood pressure. The leucocyte count in periferal blood fell markedly, reaching a minimun within one hour after infusion of either of the substances.Signs that could be interpreted as a progressive disseminated intravascular coagulation with decrease of fibrinogen and platelet count was observed after kallikrein as well as bradykinin infusions. A pronounced increase of the plasma tissue plasminogen activat
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Kindel, G., and J. Fareed. "MODULATORY EFFECT OF SERINE PROTEASES AND RELATED ENZYMES ON ISOLATED SMOOTH MUSCLE PREPARATIONS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644602.

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Thrombin and related proteases produce varying pharmacologic responses in animal models. To more specifically study the in vivo actions of thrombin and related proteases, we have used isolated tissue preparations of the rabbit aortic strip (RAS), isolated guinea pig ileum (GPI) and isolated rat uterus (RU). Standard tissue-agonist regimens include epinephrine, thromboxane B2 with RAS; bradykinin, acetylcholine, histamine and serotonin with GPI; and acetylcholine, bradykinin and angiotensin with RU. The smooth muscle modulant action of numerous proteinases were screened in these regimens by bra
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4

Ricciardolo, Fabio L. M., Sabrina Benedetto, Ilaria Defilippi, et al. "Over-Expression Of Bradykinin B1 And B2 Receptors In Bronchial Mucosa Of Severe Asthma: Relation To Airway Remodeling." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a2415.

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