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血管紧张素 II 亚型 2 受体更新:聚焦肽类和非肽类激动剂。

Update on Angiotensin II Subtype 2 Receptor: Focus on Peptide and Nonpeptide Agonists.

机构信息

College of Pharmacy, Idaho State University, Pocatello, Idaho, USA.

College of Pharmacy, Idaho State University, Pocatello, Idaho, USA

出版信息

Mol Pharmacol. 2021 Jun;99(6):469-487. doi: 10.1124/molpharm.121.000236. Epub 2021 Apr 1.

DOI:10.1124/molpharm.121.000236
PMID:33795351
Abstract

Angiotensin II (Ang II) is the most dominant effector component of the renin-angiotensin system (RAS) that generally acts through binding to two main classes of G protein-coupled receptors, namely Ang II subtype 1 receptor (AT1R) and angiotensin II subtype 2 receptor (AT2R). Despite some controversial reports, the activation of AT2R generally antagonizes the effects of Ang II binding on AT1R. Studying AT2R signaling, function, and its specific ligands in cell culture or animal studies has confirmed its beneficial effects throughout the body. These characteristics classify AT2R as part of the protective arm of the RAS that, along with functions of Ang (1-7) through Mas receptor signaling, modulates the harmful effects of Ang II on AT1R in the activated classic arm of the RAS. Although Ang II is the primary ligand for AT2R, we have summarized other natural or synthetic peptide and nonpeptide agonists with critical evaluation of their structure, mechanism of action, and biologic activity. SIGNIFICANCE STATEMENT: AT2R is one of the main components of the RAS and has a significant prospective for mediating the beneficial action of the RAS through its protective arm on the body's homeostasis. Targeting AT2R offers substantial clinical application possibilities for modulating various pathological conditions. This review provided concise information regarding the AT2R peptide and nonpeptide agonists and their potential clinical applications for various diseases.

摘要

血管紧张素 II(Ang II)是肾素-血管紧张素系统(RAS)中最主要的效应成分,通常通过与两种主要的 G 蛋白偶联受体结合而发挥作用,即血管紧张素 II 亚型 1 受体(AT1R)和血管紧张素 II 亚型 2 受体(AT2R)。尽管有一些争议性的报告,但 AT2R 的激活通常拮抗 Ang II 与 AT1R 结合的作用。在细胞培养或动物研究中研究 AT2R 信号转导、功能及其特定配体,已证实其在全身具有有益作用。这些特征将 AT2R 归类为 RAS 的保护臂的一部分,与 Ang(1-7)通过 Mas 受体信号转导的功能一起,调节 RAS 的激活经典臂中 Ang II 对 AT1R 的有害作用。尽管 Ang II 是 AT2R 的主要配体,但我们已经总结了其他天然或合成肽和非肽激动剂,并对其结构、作用机制和生物活性进行了批判性评估。意义陈述:AT2R 是 RAS 的主要组成部分之一,通过其对身体内稳态的保护臂,对 RAS 的有益作用具有重要的介导作用。靶向 AT2R 为调节各种病理状况提供了大量的临床应用可能性。本综述提供了有关 AT2R 肽和非肽激动剂及其在各种疾病中的潜在临床应用的简洁信息。

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