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血管紧张素 II 信号转导:对生理和病理生理学机制的最新研究。

Angiotensin II Signal Transduction: An Update on Mechanisms of Physiology and Pathophysiology.

机构信息

Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University , Philadelphia, Pennsylvania ; Department of Pharmacology and Toxicology, School of Medicine, University of Mississippi Medical Center , Jackson, Mississippi ; Department of Pharmacology, Center for Hypertension Research, Roy J. and Lucille A. Carver College of Medicine, University of Iowa , Iowa City, Iowa ; and Duke-NUS, Singapore and Department of Medicine, Duke University Medical Center , Durham, North Carolina.

出版信息

Physiol Rev. 2018 Jul 1;98(3):1627-1738. doi: 10.1152/physrev.00038.2017.

Abstract

The renin-angiotensin-aldosterone system plays crucial roles in cardiovascular physiology and pathophysiology. However, many of the signaling mechanisms have been unclear. The angiotensin II (ANG II) type 1 receptor (ATR) is believed to mediate most functions of ANG II in the system. ATR utilizes various signal transduction cascades causing hypertension, cardiovascular remodeling, and end organ damage. Moreover, functional cross-talk between ATR signaling pathways and other signaling pathways have been recognized. Accumulating evidence reveals the complexity of ANG II signal transduction in pathophysiology of the vasculature, heart, kidney, and brain, as well as several pathophysiological features, including inflammation, metabolic dysfunction, and aging. In this review, we provide a comprehensive update of the ANG II receptor signaling events and their functional significances for potential translation into therapeutic strategies. ATR remains central to the system in mediating physiological and pathophysiological functions of ANG II, and participation of specific signaling pathways becomes much clearer. There are still certain limitations and many controversies, and several noteworthy new concepts require further support. However, it is expected that rigorous translational research of the ANG II signaling pathways including those in large animals and humans will contribute to establishing effective new therapies against various diseases.

摘要

肾素-血管紧张素-醛固酮系统在心血管生理学和病理生理学中起着至关重要的作用。然而,许多信号机制尚不清楚。血管紧张素 II(ANG II)受体 1(ATR)被认为介导了该系统中 ANG II 的大多数功能。ATR 利用各种信号转导级联反应导致高血压、心血管重塑和终末器官损伤。此外,ATR 信号通路与其他信号通路之间的功能串扰已得到认可。越来越多的证据揭示了 ANG II 信号转导在血管、心脏、肾脏和大脑的病理生理学中的复杂性,以及包括炎症、代谢功能障碍和衰老在内的几种病理生理特征。在这篇综述中,我们全面更新了 ANG II 受体信号事件及其在潜在转化为治疗策略中的功能意义。ATR 仍然是该系统介导 ANG II 生理和病理生理功能的核心,特定信号通路的参与变得更加清晰。仍然存在一定的局限性和许多争议,一些值得注意的新概念需要进一步的支持。然而,预计包括大型动物和人类在内的 ANG II 信号通路的严格转化研究将有助于建立针对各种疾病的有效新疗法。

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