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机构地区:[1]复旦大学上海医学院生理学与病理生理学系 [2]杭州师范学院生理学教研室,杭州310018 [3]香港中文大学医学院生理学系,中国香港新界沙田
出 处:《生理科学进展》2007年第1期43-48,共6页Progress in Physiological Sciences
摘 要:血管紧张素转换酶2(ACE2)和Mas受体的发现使人们对肾素-血管紧张素(RAS)有了更全面的认识。ACE2可水解血管紧张素Ⅰ和血管紧张素Ⅱ直接或间接生成血管紧张素1-7(Ang1-7),并与高血压的形成密切相关。Ang1-7主要通过Mas受体引起血管舒张、抑制细胞增殖。ACE2-Ang1-7-Mas轴的发现为RAS的研究、高血压等心血管疾病的防治和新药开发提供了新的思路和方向。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-converring enzyme (ACE) generates angiotensin 1-7 directly through cleaving angiotensin Ⅱ, or indirectly through angiotensin Ⅰin the body. Ang 1-7 exhibits vasodilatory and antiproliferative effects, and these effects were mainly mediated by Mas receptor. So ACE2-angiotensinl-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.
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