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血管紧张素转换酶抑制剂的比较特性:与组织血管紧张素转换酶抑制作用的关系及潜在临床意义。

Comparative properties of angiotensin-converting enzyme inhibitors: relations with inhibition of tissue angiotensin-converting enzyme and potential clinical implications.

作者信息

Nash D T

出版信息

Am J Cardiol. 1992 Apr 2;69(10):26C-32C. doi: 10.1016/0002-9149(92)90278-7.

Abstract

This review summarizes the evidence indicating that local synthesis of angiotensin II, and interference with this process by inhibition of angiotensin-converting enzyme (ACE), may be important in the treatment of hypertension. Inhibition of tissue converting enzyme generally has a stronger correlation with the hemodynamic effects of ACE inhibitors than inhibition of ACE in plasma. Reported differences in the ability of ACE inhibitors to penetrate tissues and to bind to the converting enzyme may be closely related to the relative lipophilicity of these agents. Finally, correlation of data from clinical studies with results provided by laboratory experimentation suggests that the efficacy of different ACE inhibitors in hypertensive patients may be predicted from differences among the actions of these drugs in vitro and in whole animals.

摘要

本综述总结了相关证据,表明血管紧张素II的局部合成以及通过抑制血管紧张素转换酶(ACE)对这一过程的干扰在高血压治疗中可能具有重要意义。与抑制血浆中的ACE相比,抑制组织转换酶通常与ACE抑制剂的血流动力学效应具有更强的相关性。据报道,ACE抑制剂穿透组织和与转换酶结合的能力差异可能与这些药物的相对亲脂性密切相关。最后,临床研究数据与实验室实验结果的相关性表明,不同ACE抑制剂在高血压患者中的疗效可以根据这些药物在体外和整体动物中的作用差异来预测。

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