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肾素-血管紧张素系统 ACE2/Ang(1-7)/Mas 受体轴在心肌缺血再灌注损伤中的作用。

The function of the ACE2/Ang(1-7)/Mas receptor axis of the renin-angiotensin system in myocardial ischemia reperfusion injury.

机构信息

Institute of Cardiovascular Disease, Key Laboratory for Arteriosclerology of Hunan Province, Hunan International Scientific and Technological Cooperation Base of Arteriosclerotic Disease, Hengyang Medical College, University of South China, Hengyang, Hunan, PR China.

出版信息

Eur Rev Med Pharmacol Sci. 2022 Mar;26(6):1852-1859. doi: 10.26355/eurrev_202203_28330.

Abstract

OBJECTIVE

Angiotensin-converting enzyme 2(ACE2) is a critical element of the renin-angiotensin system (RAS), which can convert angiotensin (Ang)II to Ang(1-7), followed by binding Mas receptor (MasR) and subsequently produces cardioprotective effects through various signal transduction pathways. It has been discovered in research that activation of the RAS contributes a crucial influence during the myocardial ischemia reperfusion injury (MIRI) development. The features of ACE2, Ang(1-7), and MasR, as well as the function of the ACE2/Ang(1-7)/MasR axis in MIRI, are discussed in our review, with the therapeutic potential of this axis as a new treatment option for MIRI patients shown.

MATERIALS AND METHODS

To retrieve a thorough collection of studies, we performed a search in PubMed using the following combination of keywords: (ACE2) or (Ang1-7) or (Mas receptor) and (Myocardial Ischemia reperfusion injury). The time limits used for the search were 1986 to 2021.

RESULTS

In total, 367 articles were included. Titles and abstracts of articles were screened for relevance, and all relevant articles published in English were included.

CONCLUSIONS

ACE2, a prominent member of the RAS, performs a crucial regulatory function in the cardiovascular system. ACE2 regulates the RAS inversely mainly by hydrolyzing the harmful AngII to the beneficial Ang(1-7). Increasing or activating ACE2 or Ang(1-7) may help prevent and treat MIRI. However, additional research into the specific processes behind the ACE2/Ang(1-7)/MasR axis in MIRI is necessary, as well as the performance of additional in-depth studies to go from basic research to clinical translation.

摘要

目的

血管紧张素转换酶 2(ACE2)是肾素-血管紧张素系统(RAS)的关键组成部分,它可以将血管紧张素(Ang)II 转化为 Ang(1-7),然后与 Mas 受体(MasR)结合,随后通过各种信号转导途径产生心脏保护作用。研究发现,RAS 的激活对心肌缺血再灌注损伤(MIRI)的发展有至关重要的影响。本文综述了 ACE2、Ang(1-7)和 MasR 的特征,以及 ACE2/Ang(1-7)/MasR 轴在 MIRI 中的作用,并展示了该轴作为 MIRI 患者新的治疗选择的治疗潜力。

材料和方法

为了全面检索研究,我们在 PubMed 中使用以下关键词组合进行搜索:(ACE2)或(Ang1-7)或(Mas 受体)和(心肌缺血再灌注损伤)。搜索时间限制为 1986 年至 2021 年。

结果

共纳入 367 篇文章。筛选文章的标题和摘要以确定相关性,并纳入所有以英文发表的相关文章。

结论

ACE2 是 RAS 的重要成员,在心血管系统中发挥着关键的调节作用。ACE2 主要通过水解有害的 AngII 产生有益的 Ang(1-7)来调节 RAS。增加或激活 ACE2 或 Ang(1-7)可能有助于预防和治疗 MIRI。然而,需要进一步研究 MIRI 中 ACE2/Ang(1-7)/MasR 轴的具体过程,以及从基础研究到临床转化的进一步深入研究。

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