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血管紧张素-(1-9)在高血压中的作用。

Angiotensin-(1-9) in hypertension.

机构信息

Advanced Center for Chronic Diseases (ACCDiS), Faculty of Chemical & Pharmaceutical Sciences and Faculty of Medicine, University of Chile, Santiago, Chile.

Advanced Center for Chronic Diseases (ACCDiS), Faculty of Chemical & Pharmaceutical Sciences and Faculty of Medicine, University of Chile, Santiago, Chile; Network for the Study of High-lethality Cardiopulmonary Diseases (REECPAL), Universidad de Chile, Santiago, Chile.

出版信息

Biochem Pharmacol. 2022 Sep;203:115183. doi: 10.1016/j.bcp.2022.115183. Epub 2022 Jul 21.

DOI:10.1016/j.bcp.2022.115183
PMID:35870482
Abstract

Angiotensin-(1-9) [Ang-(1-9)] is a peptide of the non-canonical renin-angiotensin system (RAS) synthesized from angiotensin I by the monopeptidase angiotensin-converting enzyme type 2 (ACE2). Using osmotic minipumps, infusion of Ang-(1-9) consistently reduces blood pressure in several rat hypertension models. In these animals, hypertension-induced end-organ damage is also decreased. Several pieces of evidence suggest that Ang-(1-9) is the endogenous ligand that binds and activates the type-2 angiotensin II receptor (AT2R). Activation of AT2R triggers different tissue-specific signaling pathways. This phenomenon could be explained by the ability of AT2R to form different heterodimers with other G protein-coupled receptors. Because of the antihypertensive and protective effects of AT2R activation by Ang-(1-9), associated with a short half-life of RAS peptides, several synthetic AT2R agonists have been synthesized and assayed. Some of them, particularly CGP42112, C21 and novokinin, have demonstrated antihypertensive properties. Only two synthetic AT2R agonists, C21 and LP2-3, have been tested in clinical trials, but none of them like an antihypertensive. Therefore, Ang-(1-9) is a promising antihypertensive drug that reduces hypertension-induced end-organ damage. However, further research is required to translate this finding successfully to the clinic.

摘要

血管紧张素-(1-9)[Ang-(1-9)]是由血管紧张素 I 通过单肽酶血管紧张素转换酶 2 (ACE2) 合成的非经典肾素-血管紧张素系统 (RAS) 的一种肽。使用渗透微型泵,血管紧张素-(1-9) 的输注可一致降低几种大鼠高血压模型中的血压。在这些动物中,高血压引起的靶器官损伤也减少。有几项证据表明,Ang-(1-9) 是与型 2 血管紧张素 II 受体 (AT2R) 结合并激活其的内源性配体。AT2R 的激活触发不同的组织特异性信号通路。这种现象可以通过 AT2R 与其他 G 蛋白偶联受体形成不同的异二聚体的能力来解释。由于 Ang-(1-9) 激活 AT2R 具有降压和保护作用,以及 RAS 肽的半衰期短,因此已经合成并检测了几种合成的 AT2R 激动剂。其中一些,特别是 CGP42112、C21 和 novokinin,已被证明具有降压作用。只有两种合成的 AT2R 激动剂,C21 和 LP2-3,已经在临床试验中进行了测试,但它们都没有像降压药那样有效。因此,Ang-(1-9) 是一种有前途的降压药物,可降低高血压引起的靶器官损伤。然而,需要进一步的研究才能成功将这一发现转化为临床应用。

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