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血管紧张素受体-中性内肽酶抑制作用

Angiotensin Receptor-Neprilysin Inhibition.

作者信息

Havakuk Ofer, Elkayam Uri

机构信息

1 Division of Cardiovascular Medicine, Department of Medicine, LAC/USC Medical Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.

出版信息

J Cardiovasc Pharmacol Ther. 2017 Jul;22(4):356-364. doi: 10.1177/1074248416683049. Epub 2016 Dec 28.

Abstract

The novel combination sacubitril/valsartan represents a new therapeutic approach in the management of heart failure. With the simultaneous blockage of the enzyme neprilysin (by sacubitril) and angiotensin II receptors (by valsartan), this combination reduces the degradation of natriuretic peptides and other counterregulatory peptide systems while avoiding the deleterious effect of angiotensin II receptors activation and thereby encompasses a beneficial impact of 2 important neurohormonal pathways activated in heart failure. As opposed to previously tested neprilysin inhibitors, sacubitril/valsartan represents a more effective method in reducing morbidity and mortality in heart failure, while preserving a safety profile comparable to well-established, standard, angiotensin-converting enzyme inhibitor's therapy.

摘要

新型组合药物沙库巴曲/缬沙坦代表了心力衰竭管理中的一种新治疗方法。通过(沙库巴曲)同时抑制中性肽链内切酶和(缬沙坦)阻断血管紧张素II受体,这种组合减少了利钠肽和其他抗调节肽系统的降解,同时避免了血管紧张素II受体激活的有害影响,从而涵盖了心力衰竭中激活的2条重要神经激素途径的有益作用。与先前测试的中性肽链内切酶抑制剂不同,沙库巴曲/缬沙坦是降低心力衰竭发病率和死亡率的更有效方法,同时保持与成熟的标准血管紧张素转换酶抑制剂疗法相当的安全性。

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