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首页> 外文期刊>British Journal of Pharmacology >Long-term bradycardia caused by atrioventricular block can remodel the canine heart to detect the histamine H_1 blocker terfenadine-induced torsades de pointes arrhythmias
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Long-term bradycardia caused by atrioventricular block can remodel the canine heart to detect the histamine H_1 blocker terfenadine-induced torsades de pointes arrhythmias

机译:房室传导阻滞引起的长期心动过缓可以重塑犬心脏,以检测组胺H_1阻滞剂替非那定引起的点性心律失常

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1 Although a second-generation histamine H_1 blocker terfenadine induced torsades de pointes (TdP) arrhythmias in patients via the blockade of a rapid component of delayed rectifier K~+ current (I_(Kr)), such action of terfenadine has not been detected in previous animal models. 2 We analysed the potential of the canine persistent atrioventricular block heart, a new in vivo proarrhythmia model, to detect a torsadogenic effect of terfenadine of an oral dose of 3 or 30 mg kg~(-1). The doses can provide therapeutic to supra-therapeutic plasma concentrations as an anti-histamine. 3 In 2 weeks of bradycardiac heart model, there were no significant changes in any of the electrocardiogram parameters after the administration of both doses of terfenadine. 4 In 4-6 weeks of bradycardiac heart model, the low dose of terfenadine hardly affected any of the electrocardiogram parameters except that it induced TdP in one out of six animals. The high dose significantly decreased the atrial rate and ventricular rate, prolonged the QT interval, and induced TdP in five out of six animals. Moreover, temporal variability of repolarization increased after the high-dose administration. 5 These results suggest that long-term bradycardia caused by atrioventricular block can remodel the canine heart to detect terfenadine-induced TdP.
机译:1尽管第二代组胺H_1阻滞剂特非那定通过阻断快速整流器K〜+电流的快速成分(I_(Kr))引起患者的扭转性心律失常(TdP),但尚未在患者中检测到这种特非那定的作用以前的动物模型。 2我们分析了一种新的体内心律失常模型犬持续性房室传导阻滞心脏检测口服剂量为3或30 mg kg〜(-1)的替非那定具有致畸作用的潜力。所述剂量可以提供治疗上至治疗上的血浆浓度作为抗组胺药。 3在心动过缓的心脏模型的2周中,两种剂量的非非那定给药后,任何心电图参数均无明显变化。 4在心动过缓心脏模型的4到6周内,低剂量的fenfenadine几乎不会影响任何心电图参数,只是它会在六分之一的动物中诱发TdP。高剂量显着降低了六只动物中五只的心房率和心室率,延长了QT间隔,并诱导了TdP。此外,大剂量给药后复极的时间变异性增加。 5这些结果表明,由房室传导阻滞引起的长期心动过缓可以重塑犬的心脏,以检测特非那定诱导的TdP。

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