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血管紧张素 II 型受体激动剂:它们应该应用在哪些地方?

Angiotensin II type 2 receptor agonists: where should they be applied?

机构信息

Erasmus Medical Center, Division of Vascular Medicine and Pharmacology, Department of Internal Medicine, Rotterdam, The Netherlands.

出版信息

Expert Opin Investig Drugs. 2012 Apr;21(4):501-13. doi: 10.1517/13543784.2012.664131. Epub 2012 Feb 21.

Abstract

INTRODUCTION

Angiotensin II, the active endproduct of the renin-angiotensin system (RAS), exerts its effects via angiotensin II type 1 and type 2 (AT(1), AT(2)) receptors. AT(1) receptors mediate all well-known effects of angiotensin II, ranging from vasoconstriction to tissue remodeling. Thus, to treat cardiovascular disease, RAS blockade aims at preventing angiotensin II-AT(1) receptor interaction. Yet RAS blockade is often accompanied by rises in angiotensin II, which may exert beneficial effects via AT(2) receptors.

AREAS COVERED

This review summarizes our current knowledge on AT(2) receptors, describing their location, function(s), endogenous agonist(s) and intracellular signaling cascades. It discusses the beneficial effects obtained with C21, a recently developed AT(2) receptor agonist. Important questions that are addressed are do these receptors truly antagonize AT(1) receptor-mediated effects? What about their role in the diseased state and their heterodimerization with other receptors?

EXPERT OPINION

The general view that AT(2) receptors exclusively exert beneficial effects has been challenged, and in pathological models, their function sometimes mimics that of AT(1) receptors, for example, inducing vasoconstriction and cardiac hypertrophy. Yet given its upregulation in various pathological conditions, the AT(2) receptor remains a promising target for treatment, allowing effects beyond blood pressure-lowering, for example, in stroke, aneurysm formation, inflammation and myocardial fibrosis.

摘要

简介

血管紧张素 II(Angiotensin II)是肾素-血管紧张素系统(Renin-Angiotensin System,RAS)的活性终产物,通过血管紧张素 II 型 1 和 2(AT(1), AT(2))受体发挥作用。AT(1) 受体介导血管紧张素 II 的所有已知作用,从血管收缩到组织重塑。因此,为了治疗心血管疾病,RAS 阻断旨在防止血管紧张素 II-AT(1)受体相互作用。然而,RAS 阻断通常伴随着血管紧张素 II 的升高,血管紧张素 II 可能通过 AT(2)受体发挥有益作用。

涵盖领域

本综述总结了我们目前对 AT(2)受体的认识,描述了其位置、功能、内源性激动剂和细胞内信号转导级联。它讨论了最近开发的 AT(2)受体激动剂 C21 所获得的有益效果。所涉及的重要问题是这些受体是否真的拮抗 AT(1)受体介导的作用?它们在疾病状态下的作用及其与其他受体的异二聚化如何?

专家意见

AT(2)受体仅发挥有益作用的普遍观点受到了挑战,在病理模型中,其功能有时类似于 AT(1)受体,例如引起血管收缩和心肌肥厚。然而,鉴于其在各种病理条件下的上调,AT(2)受体仍然是治疗的有前途的靶点,除了降低血压外,还能产生影响,例如在中风、动脉瘤形成、炎症和心肌纤维化中。

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