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在兔尖端扭转型室速心脏模型中抗精神病药物舍吲哚的电生理特性:尽管QT间期延长,但致尖端扭转型室速潜力较低。

Electrophysiologic characterization of the antipsychotic drug sertindole in a rabbit heart model of torsade de pointes: low torsadogenic potential despite QT prolongation.

作者信息

Eckardt Lars, Breithardt Günter, Haverkamp Wilhelm

机构信息

Hospital of the Westfälische Wilhelms-University, Department of Cardiology and Angiology and Institute for Arteriosclerosis Research, Münster, Germany.

出版信息

J Pharmacol Exp Ther. 2002 Jan;300(1):64-71. doi: 10.1124/jpet.300.1.64.

Abstract

There is growing concern that antipsychotic drugs that prolong the QT interval almost always increase the risk for patients to develop life-threatening ventricular tachyarrhythmias (VTs) of the torsade de pointes type. We therefore sought to compare the electrophysiologic effects of the psychotropic agent sertindole, which prolongs cardiac repolarization by inhibiting the rapid component of the delayed rectifier potassium current (I(Kr)) but has a low torsadogenic potential to the antiarrhythmic agent dl-sotalol. In 18 Langendorff-perfused rabbit hearts, sotalol (10 microM, n = 8) and sertindole (0.5, 1.0, and 1.5 microM; n = 10) led to significant and comparable QT prolongation. In the presence of sotalol, torsade de pointes reproducibly occurred in atrioventricular node-blocked hearts after lowering the potassium concentration to 1.5 mM. High doses of sertindole (1.5 microM) only caused monomorphic VT (n = 4) and nonsustained polymorphic VT (n = 2) in the presence of QRS prolongation. Multiple simultaneous epi- and endocardial monophasic action potentials and a volume-conducted ECG demonstrated widening of the T/U wave, early afterdepolarizations, and increased dispersion of repolarization in the presence of dl-sotalol. In contrast to sotalol, QT and monophasic action potential prolongation were cycle length-independent in the presence of sertindole. Sertindole had no significant effect on transmural or interventricular dispersion of repolarization. Early afterdepolarizations did not occur. Despite comparable QT prolongation, sertindole did not display the proarrhythmic profile typical of other blockers of I(Kr) such as dl-sotalol. It is likely that a different mode of interaction between sertindole and the channel and/or additional pharmacological effects of sertindole, e.g., its ability to inhibit I(Na) and/or its ability to block alpha(1)-receptors, play a role.

摘要

人们越来越担心,延长QT间期的抗精神病药物几乎总是会增加患者发生危及生命的尖端扭转型室性心动过速(VT)的风险。因此,我们试图比较精神药物舍吲哚与抗心律失常药物dl-索他洛尔的电生理效应。舍吲哚通过抑制延迟整流钾电流(I(Kr))的快速成分来延长心脏复极化,但致尖端扭转的可能性较低。在18个Langendorff灌注兔心脏中,索他洛尔(10 microM,n = 8)和舍吲哚(0.5、1.0和1.5 microM;n = 10)导致QT间期显著且相当程度的延长。在索他洛尔存在的情况下,将钾浓度降至1.5 mM后,房室结阻滞的心脏中可重复性地出现尖端扭转型室性心动过速。高剂量的舍吲哚(1.5 microM)仅在QRS波增宽的情况下导致单形性室性心动过速(n = 4)和非持续性多形性室性心动过速(n = 2)。多个同时记录的体表和心内膜单相动作电位以及容积传导心电图显示,在dl-索他洛尔存在的情况下,T/U波增宽、早期后除极以及复极化离散度增加。与索他洛尔不同,在舍吲哚存在的情况下,QT间期和单相动作电位的延长与心动周期长度无关。舍吲哚对复极化的跨壁或心室内离散度没有显著影响。未出现早期后除极。尽管QT间期延长程度相当,但舍吲哚并未表现出其他I(Kr)阻滞剂(如dl-索他洛尔)典型的促心律失常特征。舍吲哚与通道之间不同的相互作用模式和/或舍吲哚的其他药理作用,例如其抑制I(Na)的能力和/或阻断α(1)受体的能力,可能起了作用。

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