Liu Cui-Qing, Huang Yu, Lu Li-Min
Department of Physiology and Pathophysiology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Sheng Li Ke Xue Jin Zhan. 2007 Jan;38(1):43-8.
The recent identification of angiotensin-converting enzyme 2 (ACE2) and Mas receptor opened new recognition of renin-angiotensin system (RAS). ACE2, a homologue of angiotensin-converting enzyme (ACE) generates angiotensin 1-7 directly through cleaving angiotensin II, or indirectly through angiotensin I in the body. Ang 1-7 exhibits vasodilatory and antiproliferative effects, and these effects were mainly mediated by Mas receptor. So ACE2-angiotensin1-7- Mas axis was considered a negative regulation in renin angiotensin system (RAS), and its significance has been implicated into hypertension and other cardiovascular diseases. The identification of the axis opens a new potential venue for further study and understanding of RAS.
血管紧张素转换酶2(ACE2)和Mas受体的近期发现开启了对肾素-血管紧张素系统(RAS)的新认识。ACE2是血管紧张素转换酶(ACE)的同源物,在体内可直接通过切割血管紧张素II生成血管紧张素1-7,或间接通过血管紧张素I生成。血管紧张素1-7具有血管舒张和抗增殖作用,这些作用主要由Mas受体介导。因此,ACE2-血管紧张素1-7-Mas轴被认为是肾素-血管紧张素系统(RAS)中的负调节机制,其在高血压和其他心血管疾病中的意义已得到证实。该轴的发现为进一步研究和理解RAS开辟了新的潜在途径。