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心力衰竭的首创血管紧张素受体脑啡肽酶抑制剂。

First-in-class angiotensin receptor neprilysin inhibitor in heart failure.

机构信息

School of Pharmacy, University of Wisconsin, Madison, Wisconsin, USA.

出版信息

Clin Pharmacol Ther. 2013 Oct;94(4):445-8. doi: 10.1038/clpt.2013.146. Epub 2013 Jul 19.

Abstract

Neprilysin inhibitors augment the natriuretic peptide system by preventing the breakdown of atrial natriuretic peptide and B-type natriuretic peptide. LCZ696, an angiotensin receptor neprilysin inhibitor composed of a neprilysin inhibitor prodrug and the angiotensin receptor antagonist valsartan, has proven effective in hypertension, has shown promise in a pilot trial of heart failure with preserved ejection fraction, and is being tested in a large outcomes trial of heart failure with reduced ejection fraction. A preserved ejection fraction outcomes trial is beginning.

摘要

利钠肽系统抑制剂通过阻止心房利钠肽和 B 型利钠肽的分解来增强利钠肽系统。LCZ696 是一种血管紧张素受体脑啡肽酶抑制剂,由脑啡肽酶抑制剂前药和血管紧张素受体拮抗剂缬沙坦组成,已被证明在高血压中有效,在心衰伴射血分数保留的试验中显示出前景,并且正在心衰伴射血分数降低的大型结局试验中进行测试。一项射血分数保留结局试验正在开始。

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