Batlle Daniel, Soler María José, Wysocki Jan
Division of Nephrology and Hypertension, Department of Medicine, The Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Curr Opin Nephrol Hypertens. 2008 May;17(3):250-7. doi: 10.1097/MNH.0b013e3282f945c2.
Whereas angiotensin-converting enzyme promotes the formation of angiotensin II, angiotensin-converting enzyme 2 promotes the degradation of angiotensin II to angiotensin-(1-7). We review recent studies dealing with angiotensin-converting enzyme 2 in kidney disease and hypertension, and discuss the potential therapeutic benefit of increasing angiotensin-converting enzyme 2 activity in the treatment of these diseases.
In glomeruli from diabetic mice, angiotensin-converting enzyme 2 expression is downregulated, and pharmacological inhibition of angiotensin-converting enzyme 2 leads to worsening of albuminuria, increased mesangial matrix deposition and fibronectin expression. The deletion of the angiotensin-converting enzyme 2 gene in mice leads to worsening of angiotensin II-induced hypertension and has also been shown to cause glomerulosclerosis in aging male mice.
Angiotensin-converting enzyme 2 is a key enzyme in the renin-angiotensin system that favors the degradation of angiotensin I and angiotensin II. Angiotensin-converting enzyme 2 inhibition by pharmacological means and by genetic deletion worsens kidney disease in diabetic mice. Strategies geared to increasing angiotensin-converting enzyme 2 activity may provide a novel therapeutic target within the renin-angiotensin system by enhancing angiotensin II degradation that may complement the current approach of inhibiting angiotensin II formation and action. Amplifying angiotensin-converting enzyme 2 activity may have a potential therapeutic role for kidney disease and hypertension.
血管紧张素转换酶促进血管紧张素II的形成,而血管紧张素转换酶2则促进血管紧张素II降解为血管紧张素 -(1 - 7)。我们综述了近期有关血管紧张素转换酶2在肾脏疾病和高血压方面的研究,并讨论了增加血管紧张素转换酶2活性在治疗这些疾病中的潜在治疗益处。
在糖尿病小鼠的肾小球中,血管紧张素转换酶2的表达下调,对血管紧张素转换酶2进行药理抑制会导致蛋白尿恶化、系膜基质沉积增加和纤连蛋白表达增多。小鼠体内血管紧张素转换酶2基因的缺失会导致血管紧张素II诱导的高血压恶化,并且在老年雄性小鼠中还会导致肾小球硬化。
血管紧张素转换酶2是肾素 - 血管紧张素系统中的关键酶,有利于血管紧张素I和血管紧张素II的降解。通过药理手段和基因缺失抑制血管紧张素转换酶2会使糖尿病小鼠的肾脏疾病恶化。旨在增加血管紧张素转换酶2活性的策略可能通过增强血管紧张素II的降解为肾素 - 血管紧张素系统提供一个新的治疗靶点,这可能补充目前抑制血管紧张素II形成和作用的方法。增强血管紧张素转换酶2的活性可能对肾脏疾病和高血压具有潜在的治疗作用。