Wright John W, Yamamoto Brent J, Harding Joseph W
Department of Psychology, Washington State University, P.O. Box 644820, Pullman, WA 99164-4820, USA.
Prog Neurobiol. 2008 Feb;84(2):157-81. doi: 10.1016/j.pneurobio.2007.10.009. Epub 2007 Nov 19.
The renin-angiotensin system (RAS) mediates several classic physiologies including body water and electrolyte homeostasis, blood pressure, cyclicity of reproductive hormones and sexual behaviors, and the regulation of pituitary gland hormones. These functions appear to be mediated by the angiotensin II (AngII)/AT(1) receptor subtype system. More recently, the angiotensin IV (AngIV)/AT(4) receptor subtype system has been implicated in cognitive processing, cerebroprotection, local blood flow, stress, anxiety and depression. There is accumulating evidence to suggest an inhibitory influence by AngII acting at the AT(1) subtype, and a facilitory role by AngIV acting at the AT(4) subtype, on neuronal firing rate, long-term potentiation, associative and spatial learning, and memory. This review initially describes the biochemical pathways that permit synthesis and degradation of active angiotensin peptides and three receptor subtypes (AT(1), AT(2) and AT(4)) thus far characterized. There is vigorous debate concerning the identity of the most recently discovered receptor subtype, AT(4). Descriptions of classic and novel physiologies and behaviors controlled by the RAS are presented. This review concludes with a consideration of the emerging therapeutic applications suggested by these newly discovered functions of the RAS.
肾素-血管紧张素系统(RAS)介导多种经典生理功能,包括机体水和电解质平衡、血压、生殖激素的周期性变化及性行为,以及垂体激素的调节。这些功能似乎由血管紧张素II(AngII)/AT(1)受体亚型系统介导。最近,血管紧张素IV(AngIV)/AT(4)受体亚型系统与认知加工、脑保护、局部血流、应激、焦虑和抑郁有关。越来越多的证据表明,AngII作用于AT(1)亚型具有抑制作用,而AngIV作用于AT(4)亚型对神经元放电频率、长时程增强、联想和空间学习及记忆具有促进作用。本综述首先描述了活性血管紧张素肽的合成和降解以及迄今已鉴定的三种受体亚型(AT(1)、AT(2)和AT(4))的生化途径。关于最近发现的受体亚型AT(4)的身份存在激烈争论。本文介绍了由RAS控制的经典和新型生理功能及行为。本综述最后考虑了RAS这些新发现功能所提示的新兴治疗应用。