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本文引用的文献

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THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: G protein-coupled receptors.2019/20 年药理学简明指南:G 蛋白偶联受体。
Br J Pharmacol. 2019 Dec;176 Suppl 1(Suppl 1):S21-S141. doi: 10.1111/bph.14748.
2
THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Enzymes.2019/20 年简明药理学指南:酶。
Br J Pharmacol. 2019 Dec;176 Suppl 1(Suppl 1):S297-S396. doi: 10.1111/bph.14752.
3
Polypill for Cardiovascular Disease Prevention in an Underserved Population.用于服务不足人群心血管疾病预防的复方药。
N Engl J Med. 2019 Sep 19;381(12):1114-1123. doi: 10.1056/NEJMoa1815359.
4
Effectiveness of polypill for primary and secondary prevention of cardiovascular diseases (PolyIran): a pragmatic, cluster-randomised trial.多酚丸用于心血管疾病一级和二级预防的效果(PolyIran):一项实用、整群随机试验。
Lancet. 2019 Aug 24;394(10199):672-683. doi: 10.1016/S0140-6736(19)31791-X.
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The renin-angiotensin system: going beyond the classical paradigms.肾素-血管紧张素系统:超越经典范式
Am J Physiol Heart Circ Physiol. 2019 May 1;316(5):H958-H970. doi: 10.1152/ajpheart.00723.2018. Epub 2019 Feb 1.
6
Genetic deletion of the alamandine receptor MRGD leads to dilated cardiomyopathy in mice.遗传性缺失alamandine 受体 MRGD 可导致小鼠扩张型心肌病。
Am J Physiol Heart Circ Physiol. 2019 Jan 1;316(1):H123-H133. doi: 10.1152/ajpheart.00075.2018. Epub 2018 Oct 19.
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The depressor axis of the renin-angiotensin system and brain disorders: a translational approach.肾素-血管紧张素系统的抑制轴与脑紊乱:一种转化方法。
Clin Sci (Lond). 2018 May 25;132(10):1021-1038. doi: 10.1042/CS20180189. Print 2018 May 31.

血管紧张素转换酶抑制剂如何改变肾素-血管紧张素系统。

How ACE inhibitors transformed the renin-angiotensin system.

机构信息

NHLI, Imperial College, London, UK.

出版信息

Br J Pharmacol. 2020 Jun;177(12):2657-2665. doi: 10.1111/bph.15045. Epub 2020 Apr 12.

DOI:10.1111/bph.15045
PMID:32144755
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7236071/
Abstract

The renin-angiotensin system (RAS) now underlies the successful treatment of almost 50% of the patients in cardiovascular medicine, with serious possibilities of extension to diabetes, Alzheimer's disease and cancer. This clinical transformation started just over 50 years ago, with the unexpected identification of a bradykinin-potentiating peptide from snake venom, as a potent inhibitor of ACE which led to the development of the first synthetic inhibitor, captopril, followed by the angiotensin receptor blockers. This article analyses the transformation of the RAS into its different stages, from academic experiments to clinical use and back to the laboratory, identifying the critical events involved, both clinical and scientific. The analysis also assesses the contributions of chance, coincidence, and conviction that were crucial in this transformation. Although questions remain, the transformation of the RAS over the past five decades provides a success story for medicine, for pharmacology, and, most significantly, for patients.

摘要

肾素-血管紧张素系统(RAS)目前为心血管医学中近 50%的患者的成功治疗提供了依据,并且在糖尿病、阿尔茨海默病和癌症方面具有重要的扩展可能性。这种临床转变始于 50 多年前,从蛇毒中意外发现一种缓激肽增强肽,作为 ACE 的有效抑制剂,从而导致第一种合成抑制剂卡托普利的开发,随后是血管紧张素受体阻滞剂。本文分析了 RAS 从学术实验到临床应用再到实验室的不同阶段的转变,确定了涉及的关键事件,包括临床和科学方面。该分析还评估了在这种转变中至关重要的偶然性、巧合性和信念的作用。尽管仍存在疑问,但 RAS 在过去五十年中的转变为医学、药理学,最重要的是为患者提供了一个成功的案例。