直接肾素抑制:aliskiren的临床研究进展。

Natale Daniele Brunetti, Luisa De Gennaro, Pier Luigi Pellegrino, Andrea Cuculo, Luigi Ziccardi, Antonio Gaglione, Matteo Di Biase
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引用次数: 1

摘要

肾素-血管紧张素-醛固酮系统(RAAS)在调节血压、体积和电解质方面起着关键作用。RAAS级联的最终产物是血管紧张素II,它通过与三种已知受体类型中的一种结合而发挥多种生物活性,并具有不同的结合后果。尽管限制血管紧张素II产生和作用的传统策略取得了成功,但这些药物促进了血浆肾素活性的反射性上升,这被认为与心血管事件的发生率增加有关。为了抵消肾素活性和RAAS激活的有害后果,已经合成了几种肾素抑制剂;Aliskiren是第一个被批准用于治疗高血压的新型非肽直接肾素抑制剂。本文综述了阿利克伦的药代动力学及其在高血压中的作用,特别是关于阿利克伦与其他降压药策略比较临床疗效的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Direct renin inhibition: update on clinical investigations with aliskiren.

The renin–angiotensin–aldosterone system (RAAS) plays a pivotal role in regulating blood pressure, volume, and electrolytes. The final product of RAAS cascade is angiotensin II, which exerts diverse biological activities via binding to one of three known receptor types, with different binding consequences. Despite the success with conventional strategies to limit angiotensin II production and action, these agents promote a reflex rise in plasma renin activity, which is thought to be associated with an increased incidence of cardiovascular events. Several renin inhibitors have been synthesized in order to counteract deleterious consequences of renin activity and RAAS activation; aliskiren is the first of these new non-peptide direct renin inhibitors to be approved for the treatment of hypertension. The paper reviews pharmacokinetics of aliskiren and its role in hypertension, with particular regard to those studies that compared clinical efficacy of aliskiren in comparison and in addition to other antihypertensive drug strategies.

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