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心力衰竭中中性肽链内切酶与利钠肽调节

Neprilysin and Natriuretic Peptide Regulation in Heart Failure.

作者信息

Bayes-Genis Antoni, Morant-Talamante Nuria, Lupón Josep

机构信息

Heart Failure Clinic, Cardiology Service, Department of Medicine, UAB, Hospital Universitari Germans Trias i Pujol, Carretera del Canyet, 08916, Badalona, Barcelona, Spain.

Department of Medicine, Universitat Autonoma de Barcelona, Barcelona, Spain.

出版信息

Curr Heart Fail Rep. 2016 Aug;13(4):151-7. doi: 10.1007/s11897-016-0292-x.

Abstract

Neprilysin is acknowledged as a key player in neurohormonal regulation, a cornerstone of modern drug therapy in chronic heart failure. In the cardiovascular system, neprilysin cleaves numerous vasoactive peptides, some with mainly vasodilating effects (natriuretic peptides, adrenomedullin, bradykinin) and other with mainly vasoconstrictor effects (angiotensin I and II, endothelin-1). For decades, neprilysin has been an important biotarget. Academia and industry have combined active efforts to search for neprilysin inhibitors (NEPIs) that might be useful in clinical practice. NEPI monotherapy was initially tested with little success due to efficacy issues. Next, combination of NEPI and ACE-inhibiting activity agents were abandoned due to safety concerns. Recently, the combination of NEPI and ARB, also known as ARNI, has shown better than expected results in heart failure with reduced ejection fraction, and multitude of ongoing studies are set to prove its value across the heart failure spectrum.

摘要

中性肽链内切酶被认为是神经激素调节中的关键角色,而神经激素调节是慢性心力衰竭现代药物治疗的基石。在心血管系统中,中性肽链内切酶可裂解多种血管活性肽,其中一些主要具有血管舒张作用(利钠肽、肾上腺髓质素、缓激肽),另一些主要具有血管收缩作用(血管紧张素I和II、内皮素-1)。几十年来,中性肽链内切酶一直是一个重要的生物靶点。学术界和产业界共同积极努力寻找可能在临床实践中有用的中性肽链内切酶抑制剂(NEPIs)。由于疗效问题,NEPIs单药治疗最初的试验收效甚微。接下来,由于安全问题,NEPIs与ACE抑制活性药物的联合应用被放弃。最近,NEPIs与ARB的联合应用,即ARNI,在射血分数降低的心力衰竭中显示出比预期更好的效果,并且众多正在进行的研究将证明其在整个心力衰竭范围内的价值。

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