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奥氮平通过阻断延迟整流钾电流的快速成分来延长心脏复极化。

Olanzapine prolongs cardiac repolarization by blocking the rapid component of the delayed rectifier potassium current.

作者信息

Morissette Pierre, Hreiche Raymond, Mallet Louise, Vo Dean, Knaus Edward E, Turgeon Jacques

机构信息

Faculty of Pharmacy, Université de Montréal, Montréal, Québec, Canada.

出版信息

J Psychopharmacol. 2007 Sep;21(7):735-41. doi: 10.1177/0269881106072669. Epub 2006 Nov 8.

Abstract

Prolongation of the QT interval has been observed during treatment with olanzapine, a thienobenzodiazepine antipsychotic agent. Our objectives were 1) to characterize the effects of olanzapine on cardiac repolarization and 2) to evaluate effects of olanzapine on the major time-dependent outward potassium current involved in cardiac repolarization, namely I(Kr) (I(Kr): rapid component of the delayed rectifier potassium current).Isolated, buffer-perfused guinea pig hearts (n = 40) were stimulated at different pacing cycle lengths (150-250 msec) and exposed to olanzapine at concentrations ranging from 1 to 100 microM. Olanzapine increased monophasic action potential duration measured at 90% repolarization (MAPD90) in a concentration-dependent manner by 6.7 +/- 0.7 msec at 3 microM but by 26.0 +/- 4.3 msec at 100 microM (250 msec cycle length). Increase in MAPD(90) was also reverse frequency dependent; 30 microM olanzapine increased MAPD90 by 28.0 +/- 6.2 msec at a pacing cycle length of 250 msec but by only 18.9 +/- 2.2 msec at a pacing cycle length of 150 msec. Experiments in HERG-transfected (HERG: human ether-a-gogo-related gene) HEK293 cells (n = 36) demonstrated concentration-dependent block of the rapid component (I(Kr)) of the delayed rectifier potassium current: tail current was decreased 50% at olanzapine 3.8 microM. Olanzapine possesses direct cardiac electrophysiological effects similar to those of class III anti-arrhythmic drugs. These effects were observed at concentrations that can be measured in patients under conditions of impaired drug elimination such as renal or hepatic insufficiency, during co-administration of other CYP1A2 substrates/inhibitors or after drug overdose. These results offer a new potential explanation for QT prolonging effects observed during olanzapine treatment in patients.

摘要

在使用噻吨苯二氮䓬类抗精神病药物奥氮平治疗期间,观察到QT间期延长。我们的目标是:1)描述奥氮平对心脏复极化的影响;2)评估奥氮平对参与心脏复极化的主要时间依赖性外向钾电流,即I(Kr)(I(Kr):延迟整流钾电流的快速成分)的影响。

将分离的、用缓冲液灌注的豚鼠心脏(n = 40)以不同的起搏周期长度(150 - 250毫秒)进行刺激,并暴露于浓度范围为1至100微摩尔的奥氮平中。奥氮平以浓度依赖性方式增加在90%复极化时测量的单相动作电位持续时间(MAPD90),在3微摩尔时增加6.7±0.7毫秒,但在100微摩尔时(250毫秒周期长度)增加26.0±4.3毫秒。MAPD(90)的增加也是反向频率依赖性的;30微摩尔奥氮平在250毫秒起搏周期长度时使MAPD90增加28.0±6.2毫秒,但在150毫秒起搏周期长度时仅增加18.9±2.2毫秒。在转染了人类ether-a-gogo相关基因(HERG)的HEK293细胞(n = 36)中进行的实验表明,奥氮平对延迟整流钾电流的快速成分(I(Kr))具有浓度依赖性阻断作用:在3.8微摩尔奥氮平作用下,尾电流降低50%。奥氮平具有与III类抗心律失常药物相似的直接心脏电生理作用。在药物消除受损的患者(如肾功能或肝功能不全患者)、在同时使用其他CYP1A2底物/抑制剂或药物过量后可测量到的浓度下观察到了这些作用。这些结果为在奥氮平治疗患者期间观察到的QT延长效应提供了一个新的潜在解释。

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