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血管紧张素2型受体(AT2R):一个具有挑战性的孪生体。

Angiotensin type 2 receptor (AT2R): a challenging twin.

作者信息

Berk Bradford C

机构信息

Center for Cardiovascular Research and Department of Medicine, University of Rochester, Rochester, NY 14642, USA.

出版信息

Sci STKE. 2003 May 6;2003(181):PE16. doi: 10.1126/stke.2003.181.pe16.

Abstract

Angiotensin II (AngII) regulates such physiological responses as salt and water balance, blood pressure, and vascular tone, and thus plays a critical role in the pathogenesis of diabetes, hypertension, myocardial infarction, congestive heart failure, and stroke. These effects are mediated through at least three receptors: AT1R, AT2R, and AT4R, which are expressed under different developmental, tissue-specific, and disease-specific conditions and which couple to distinct effector pathways. Signaling through the AT1R, a classical G protein-coupled receptor, has been extensively studied and is well understood. Less is known about signaling through the AT2R, which often antagonizes the effects of signaling through the AT1R, but intriguing data are beginning to emerge concerning the signaling strategies and pathways that the AT2R employs.

摘要

血管紧张素II(AngII)调节盐和水平衡、血压及血管张力等生理反应,因此在糖尿病、高血压、心肌梗死、充血性心力衰竭及中风的发病机制中起关键作用。这些作用至少通过三种受体介导:AT1R、AT2R和AT4R,它们在不同的发育、组织特异性和疾病特异性条件下表达,并与不同的效应器途径偶联。通过经典的G蛋白偶联受体AT1R的信号传导已得到广泛研究且理解充分。关于通过AT2R的信号传导了解较少,AT2R通常拮抗通过AT1R的信号传导效应,但有关AT2R采用的信号传导策略和途径的有趣数据正开始出现。

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