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常用镇咳药物对人乙醚 - 去极化激活钾离子通道电流的影响。

Effects of common antitussive drugs on the hERG potassium channel current.

作者信息

Deisemann Heike, Ahrens Nadine, Schlobohm Irene, Kirchhoff Christian, Netzer Rainer, Möller Clemens

机构信息

Evotec AG, Hamburg, Germany.

出版信息

J Cardiovasc Pharmacol. 2008 Dec;52(6):494-9. doi: 10.1097/FJC.0b013e31818eec8d.

Abstract

A common over-the-counter (OTC) non-opioid antitussive drug, clobutinol, was recently withdrawn from the market due to its potential to induce cardiac arrhythmias by a blockade of the potassium channel coded by the human ether-à-go-go-related gene (hERG). In this study, we investigated the effects of a number of antitussive compounds on the hERG ion channel current using patch-clamp electrophysiology, and compared the effects to that of clobutinol. The compounds clobutinol, pentoxyverine, dextromethorphan, and codeine inhibited the outward current in hERG transfected cells with half-maximal inhibition concentrations (IC50) of 1.9 microM, 3.0 microM, 5.1 microM, and 97 microM, respectively. For theobromine, no significant effect on the hERG current at a concentration up to 100 microM was detected. Safety margins between the effects of the drugs on the hERG ion channel current and their calculated maximal free therapeutic plasma concentration were calculated. These results were compared to assess potential risks of the compounds to induce torsade de pointes-type arrhythmias.

摘要

一种常见的非处方(OTC)非阿片类镇咳药氯丁诺尔,最近因其可能通过阻断人类醚 - 去极化相关基因(hERG)编码的钾通道而诱发心律失常,已从市场上撤下。在本研究中,我们使用膜片钳电生理学研究了多种镇咳化合物对hERG离子通道电流的影响,并将其与氯丁诺尔的影响进行了比较。氯丁诺尔、喷托维林、右美沙芬和可待因等化合物抑制hERG转染细胞中的外向电流,其半数最大抑制浓度(IC50)分别为1.9微摩尔、3.0微摩尔、5.1微摩尔和97微摩尔。对于可可碱,在浓度高达100微摩尔时未检测到对hERG电流有显著影响。计算了药物对hERG离子通道电流的影响与其计算出的最大游离治疗血浆浓度之间的安全边际。比较这些结果以评估化合物诱发尖端扭转型心律失常的潜在风险。

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