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血管紧张素受体-脑啡肽酶抑制剂双重作用。

Dual-acting angiotensin receptor-neprilysin inhibition.

机构信息

Hypertension Unit, Hospital 12 de Octubre, Av. Córdoba s/n, Madrid, Spain.

出版信息

Curr Hypertens Rep. 2011 Feb;13(1):74-8. doi: 10.1007/s11906-010-0166-7.

DOI:10.1007/s11906-010-0166-7
PMID:21046489
Abstract

Lowering blood pressure by pharmacologic intervention reduces the incidence of cardiovascular events. Nevertheless, despite the widespread availability of effective antihypertensive medications, the vast majority of hypertensive patients worldwide continue to have inadequate blood pressure control. The development of new antihypertensive drugs could contribute to improving the hypertension control rate, and the blockade of new pathophysiologic pathways involved in blood pressure regulation would offer additional benefits. The dual inhibition of the angiotensin II receptor and neprilysin could provide clinical benefits in a range of cardiovascular diseases, including hypertension and heart failure.

摘要

通过药物干预降低血压可减少心血管事件的发生。然而,尽管有广泛可用的有效降压药物,全世界绝大多数高血压患者的血压控制仍不理想。开发新的降压药物可能有助于提高高血压控制率,而阻断新的参与血压调节的病理生理途径将带来额外的益处。血管紧张素 II 受体和 Neprilysin 的双重抑制可能为包括高血压和心力衰竭在内的一系列心血管疾病提供临床获益。

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Dual-acting angiotensin receptor-neprilysin inhibition.血管紧张素受体-脑啡肽酶抑制剂双重作用。
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1
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Lancet. 2010 Apr 10;375(9722):1255-66. doi: 10.1016/S0140-6736(09)61966-8. Epub 2010 Mar 16.
2
Pharmacokinetics and pharmacodynamics of LCZ696, a novel dual-acting angiotensin receptor-neprilysin inhibitor (ARNi).LCZ696 的药代动力学和药效学研究,一种新型的双重作用的血管紧张素受体-脑啡肽酶抑制剂(ARNi)。
J Clin Pharmacol. 2010 Apr;50(4):401-14. doi: 10.1177/0091270009343932. Epub 2009 Nov 23.
3
Novel antihypertensive agents for resistant hypertension: what does the future hold?新型抗高血压药物治疗耐药性高血压:未来如何?
Hypertens Res. 2022 Dec;45(12):1918-1928. doi: 10.1038/s41440-022-01025-9. Epub 2022 Sep 27.
4
Efficacy of sacubitril/valsartan versus olmesartan in Japanese patients with essential hypertension: a randomized, double-blind, multicenter study.沙库巴曲缬沙坦对比奥美沙坦治疗日本原发性高血压患者的疗效:一项随机、双盲、多中心研究。
Hypertens Res. 2022 May;45(5):824-833. doi: 10.1038/s41440-021-00819-7. Epub 2022 Jan 21.
5
Expanded algorithm for managing patients with acute decompensated heart failure.急性失代偿性心力衰竭患者管理的扩展算法。
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Genetics. 2014 Mar;196(3):781-97. doi: 10.1534/genetics.113.160945. Epub 2014 Jan 6.
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