肾素-血管紧张素系统
受体
血管紧张素II
血管活性
血管紧张素1
化学
肽
机制(生物学)
药理学
内科学
内分泌学
生物
医学
生物化学
物理
血压
量子力学
作者
Daniel C. Villela,Danielle G. Passos-Silva,Robson A.S. Santos
出处
期刊:Current Opinion in Nephrology and Hypertension
[Ovid Technologies (Wolters Kluwer)]
日期:2014-01-03
卷期号:23 (2): 130-134
被引量:76
标识
DOI:10.1097/01.mnh.0000441052.44406.92
摘要
Purpose of review In this article, we review the recent findings regarding a new derivative of angiotensin-(1–7) [Ang-(1–7)], alamandine, and its receptor, the Mas-related G-coupled receptor type D (MrgD) with a special emphasis on its role and how it can be formed. Recent findings Over the last decade, there have been significant conceptual changes regarding the understanding of the renin-angiotensin system (RAS). A cardioprotective axis has been elucidated by the discovery of the Mas receptor for the biologically active Ang-(1–7), and the angiotensin-converting enzyme 2 (ACE2) that coverts Ang II into Ang-(1–7). In addition, several components of the system, such as Ang-(1–12), Angiotensin A (Ang A) and the newly discovered peptide, alamandine, have been identified. Alamandine is generated by catalysis of Ang A via ACE2 or directly from Ang-(1–7). Summary Alamandine is a vasoactive peptide with similar protective actions as Ang-(1–7) that acts through the MrgD and may represent another important counter-regulatory mechanism within the RAS.
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