Ferrario C M, Iyer S N
The Hypertension and Vascular Disease Center, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1032, USA.
Regul Pept. 1998 Nov 30;78(1-3):13-8. doi: 10.1016/s0167-0115(98)00134-7.
Accumulating evidence suggests that angiotensin-(1-7) [Ang-(1-7)] is an important component of the renin-angiotensin system. As the most pleiotropic metabolite of angiotensin I (Ang I) it manifest actions which are most often the opposite of those described for angiotensin II (Ang II). Ang-(1-7) is produced from Ang I bypassing the prerequisite formation of Ang II. The generation of Ang-(1-7) is under the control of at least three enzymes, which include neprilysin, thimet oligopeptidase, and prolyl oligopeptidase depending on the tissue compartment. Both neprilysin and thimet oligopeptidase are also involved in the metabolism of bradykinin and the atrial natriuretic peptide. Moreover, recent studies suggest that in addition to Ang I and bradykinin, Ang-(1-7) is an endogenous substrate for angiotensin converting enzyme. This suggests that there is a complex relationship between the enzymatic pathways forming angiotensin II and other various vasodepressor peptides from either the renin-angiotensin system or other peptide systems. The antihypertensive actions of angiotensin-(1-7) are mediated by an angiotensin receptor that is distinct from the pharmacologically characterized AT1 or AT2 receptor subtypes. Ang-(1-7) mediates it antihypertensive effects by stimulating synthesis and release of vasodilator prostaglandins, and nitric oxide and potentiating the hypotensive effects of bradykinin.
越来越多的证据表明,血管紧张素 -(1 - 7)[Ang -(1 - 7)]是肾素 - 血管紧张素系统的重要组成部分。作为血管紧张素I(Ang I)最具多效性的代谢产物,它所表现出的作用往往与血管紧张素II(Ang II)的作用相反。Ang -(1 - 7)由Ang I生成,绕过了Ang II的必要形成过程。Ang -(1 - 7)的生成受至少三种酶的控制,这三种酶根据组织部位不同包括中性内肽酶、硫醇内肽酶和脯氨酰寡肽酶。中性内肽酶和硫醇内肽酶也参与缓激肽和心房利钠肽的代谢。此外,最近的研究表明,除了Ang I和缓激肽外,Ang -(1 - 7)还是血管紧张素转换酶的内源性底物。这表明在形成血管紧张素II以及肾素 - 血管紧张素系统或其他肽系统中其他各种血管舒张肽的酶促途径之间存在复杂的关系。血管紧张素 -(1 - 7)的降压作用由一种不同于药理学上已明确的AT1或AT2受体亚型的血管紧张素受体介导。Ang -(1 - 7)通过刺激血管舒张性前列腺素和一氧化氮的合成与释放以及增强缓激肽的降压作用来介导其降压效果。