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血管紧张素-(1-7)的中枢和外周作用。

Central and peripheral actions of angiotensin-(1-7).

作者信息

Santos R A, Campagnole-Santos M J

机构信息

Departamento de Fisiologia e Biofísica, Universidade Federal de Minas Gerais, Belo Horizonte, Brasil.

出版信息

Braz J Med Biol Res. 1994 Apr;27(4):1033-47.

PMID:8087084
Abstract
  1. In this article we review the physiological actions of the heptapeptide angiotensin-(1-7) [Ang-(1-7)] at the periphery and on central pathways involved in the control of arterial pressure. Peripherally Ang-(1-7) has been shown to present a potent antidiuretic effect on water-loaded rats. Microinjection of pmol amounts of Ang-(1-7) into the dorsomedial or ventrolateral medulla (VLM) of anesthetized rats produces cardiovascular effects comparable to Ang II. In addition, in vitro experiments have shown that Ang-(1-7) has a potent vasopressin and prostaglandin releasing activity and excites neuronal activity in the hypothalamus and medulla. 2. Evidence for the existence of a new angiotensin receptor subtype that mediates the central cardiovascular actions of this active peptide of the renin-angiotensin system (RAS) is also provided. Neither the AT1 receptor antagonist DUP 753 or the AT2 receptor antagonist CGP 42112A blocked the pressor response produced by microinjection of Ang-(1-7) into the rostral VLM. However, the effect of Ang-(1-7) on VLM was completely abolished by the non-specific angiotensin receptor antagonist, Sar1-Thr8-Ang II. 3. The data presented here reinforce the hypothesis of the existence of complex site-specific interactions between multiple angiotensins and multiple receptors in the mediation of important central and peripheral effects of the RAS.
摘要
  1. 在本文中,我们综述了七肽血管紧张素 -(1 - 7)[Ang -(1 - 7)]在周围组织以及参与动脉血压控制的中枢途径中的生理作用。在周围组织中,Ang -(1 - 7)已被证明对水负荷大鼠具有强大的抗利尿作用。向麻醉大鼠的背内侧或腹外侧延髓(VLM)微量注射pmol量的Ang -(1 - 7)会产生与血管紧张素II相当的心血管效应。此外,体外实验表明,Ang -(1 - 7)具有强大的血管加压素和前列腺素释放活性,并能刺激下丘脑和延髓的神经元活动。2. 本文还提供了证据,证明存在一种新的血管紧张素受体亚型,该亚型介导肾素 - 血管紧张素系统(RAS)中这种活性肽的中枢心血管作用。AT1受体拮抗剂DUP 753或AT2受体拮抗剂CGP 42112A均不能阻断向延髓头端VLM微量注射Ang -(1 - 7)所产生的升压反应。然而,非特异性血管紧张素受体拮抗剂Sar1 - Thr8 - Ang II可完全消除Ang -(1 - 7)对VLM的作用。3. 本文所呈现的数据强化了以下假说:在介导RAS重要的中枢和外周效应过程中,多种血管紧张素与多种受体之间存在复杂的位点特异性相互作用。

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