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血管紧张素转换酶2-血管紧张素1-7/1-9系统:心力衰竭治疗的新的有前景的靶点。

Angiotensin-converting enzyme 2-Angiotensin 1-7/1-9 system: novel promising targets for heart failure treatment.

作者信息

Kittana Naim

机构信息

Department of Biomedical Sciences, An-Najah National University, New Campus, Pharmacy Building, 2nd Floor, Akademia Street, PO Box: 7, Nablus, West-Bank, Palestine.

出版信息

Fundam Clin Pharmacol. 2018 Feb;32(1):14-25. doi: 10.1111/fcp.12318. Epub 2017 Dec 1.

Abstract

Cardiac remodeling (cardiac hypertrophy and fibrosis) is a hallmark of heart failure (HF). It can be induced by the abnormal elevation of several endogenous factors including angiotensin II (Ang II), which is generated from its precursor angiotensin I (Ang I) by the action of angiotensin-converting enzyme. The inhibition of this enzyme or the blockade of the Ang II receptors demonstrated a high clinical value against the progression of HF. Ang I and Ang II may also be converted into angiotensin 1-7 (Ang 1-7) and angiotensin 1-9 (Ang 1-9), respectively, by the action of angiotensin-converting enzyme 2. Both derivatives demonstrated a promising anticardiac remodeling activity especially against the detrimental effects of Ang II. This manuscript thoroughly reviews the available in vitro and in vivo data on Ang 1-7 and Ang 1-9 in the context of the treatment of HF and discusses the associated molecular mechanisms and the trials to clinically utilize Ang 1-7 mimetics for the treatment of that disease.

摘要

心脏重塑(心脏肥大和纤维化)是心力衰竭(HF)的一个标志。它可由几种内源性因子异常升高所诱导,包括血管紧张素II(Ang II),其由血管紧张素I(Ang I)通过血管紧张素转换酶的作用生成。抑制该酶或阻断Ang II受体对HF的进展显示出很高的临床价值。Ang I和Ang II也可分别通过血管紧张素转换酶2的作用转化为血管紧张素1-7(Ang 1-7)和血管紧张素1-9(Ang 1-9)。这两种衍生物均显示出有前景的抗心脏重塑活性,尤其是对抗Ang II的有害作用。本手稿全面综述了在HF治疗背景下关于Ang 1-7和Ang 1-9的现有体外和体内数据,并讨论了相关分子机制以及临床上利用Ang 1-7模拟物治疗该疾病的试验。

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