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首页> 外文期刊>Current opinion in nephrology and hypertension >New aspects of the renin-angiotensin system: angiotensin-converting enzyme 2 - a potential target for treatment of hypertension and diabetic nephropathy.
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New aspects of the renin-angiotensin system: angiotensin-converting enzyme 2 - a potential target for treatment of hypertension and diabetic nephropathy.

机译:肾素-血管紧张素系统的新方面:血管紧张素转化酶2-一种治疗高血压和糖尿病肾病的潜在靶标。

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PURPOSE OF REVIEW: 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. RECENT FINDINGS: 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. SUMMARY: 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.
机译:审查目的:血管紧张素转化酶促进血管紧张素II的形成,而血管紧张素转化酶2促进血管紧张素II降解为血管紧张素-(1-7)。我们回顾了有关肾脏疾病和高血压中血管紧张素转化酶2的最新研究,并讨论了增加血管紧张素转化酶2活性在这些疾病的治疗中的潜在治疗益处。最近的发现:在糖尿病小鼠的肾小球中,血管紧张素转化酶2的表达被下调,并且对血管紧张素转化酶2的药理抑制导致白蛋白尿恶化,肾小球系膜基质沉积和纤连蛋白表达。小鼠中血管紧张素转化酶2基因的缺失导致血管紧张素II诱导的高血压恶化,并且还显示出它会导致衰老的雄性小鼠肾小球硬化。简介:血管紧张素转换酶2是肾素-血管紧张素系统中的关键酶,有助于降解血管紧张素I和血管紧张素II。通过药理学方法和基因缺失抑制血管紧张素转化酶2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活性的策略可能会通过增强血管紧张素II降解来提供一种新的治疗靶标,从而补充肾素-血管紧张素II系统,从而补充目前抑制血管紧张素II形成和作用的方法。放大血管紧张素转换酶2活性可能对肾脏疾病和高血压具有潜在的治疗作用。

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