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奈普利肽抑制治疗心力衰竭:一个关于科学、机缘巧合和第二次机会的故事。

Neprilysin inhibition to treat heart failure: a tale of science, serendipity, and second chances.

机构信息

BHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

出版信息

Eur J Heart Fail. 2015 Mar;17(3):242-7. doi: 10.1002/ejhf.250.

Abstract

This review describes the role of neprilysin (also known as neutral endopeptidase or enkephalinase) in the degradation of natriuretic and other vasoactive peptides, including bradykinin and adrenomedullin. The initial development of neprilysin inhibitors, then angiotensin converting enzyme-neprilysin inhibitors and, most recently, the angiotensin receptor neprilysin inhibitor (ARNI) LCZ696 (sacubitril valsartan) as an extension of the nurohumoral basis for the treatment of heart failure is also summarised. Finally, the implications of the compelling benefits of LCZ696 compared with enalapril in the Prospective comparison of ARNI with ACEI to Determine Impact on Global Mortality and morbidity in Heart Failure trial (PARADIGM-HF) is discussed.

摘要

这篇综述描述了 Neprilysin(也称为中性内肽酶或脑啡肽酶)在降解利钠肽和其他血管活性肽(包括缓激肽和肾上腺髓质素)中的作用。还总结了 Neprilysin 抑制剂的最初发展,然后是血管紧张素转换酶 Neprilysin 抑制剂,以及最近的血管紧张素受体 Neprilysin 抑制剂(ARNI)LCZ696(沙库巴曲缬沙坦),作为治疗心力衰竭的神经激素基础的扩展。最后,讨论了与依那普利相比,LCZ696 在 Prospective comparison of ARNI with ACEI to Determine Impact on Global Mortality and morbidity in Heart Failure trial(PARADIGM-HF)中具有令人信服的益处的意义。

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