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药物安全性评价中药物诱导尖端扭转型室速的急性犬模型——麻醉的影响以及奎尼丁和阿司咪唑的验证

Acute canine model for drug-induced Torsades de Pointes in drug safety evaluation-influences of anesthesia and validation with quinidine and astemizole.

作者信息

Yamamoto K, Tamura T, Imai R, Yamamoto M

机构信息

Drug Safety Research Laboratories, Takeda Chemical Industries, Ltd., Drug Safety Research Labs, 17-85, Jusohonmachi 2-chome, Yodogawa-ku, Osaka 532-8686, Japan.

出版信息

Toxicol Sci. 2001 Mar;60(1):165-76. doi: 10.1093/toxsci/60.1.165.

Abstract

An acute in vivo model for drug-induced torsades de pointes (TdP) for use in safety evaluation of drugs was developed using dogs with acute complete atrioventricular (AV) block. In order to study the effects of anesthetic agents on the inducibility of TdP, arrhythmias were induced by programmed electrical stimulation (PES) before and after cumulative intravenous administration of quinidine under anesthesia with sodium pentobarbital, halothane, or isoflurane. Both prolongation of the QTc and the incidence of TdP were greatest in dogs anesthetized with halothane and were smallest in those given pentobarbital, suggesting that halothane is the most suitable anesthetic for this TdP model. To further validate this model, astemizole was administered intravenously to other dogs under halothane anesthesia. Astemizole at 0.3 mg/kg caused slight prolongation of the QT interval but did not induce any arrhythmias. At 1 mg/kg, however, TdP were induced in 5 of 10 animals and in an additional 2 animals at 3 mg/kg. Single and multiple ectopic beats preceded the induction of TdP, and the ectopic beats were observed in a dose-dependent manner. The plasma concentrations of quinidine in dogs with TdP were equivalent to or less than quinidine levels in humans with TdP, while those of astemizole were higher in dogs. In conclusion, this acute canine model of TdP with halothane anesthesia, complete AV block, PES, and simultaneous measurements of plasma drug concentration would be valuable for assessing the risk of drugs, especially I(Kr) blockers, to induce TdP in humans.

摘要

利用患有急性完全性房室传导阻滞的犬建立了一种用于药物安全性评价的药物诱导尖端扭转型室性心动过速(TdP)的急性体内模型。为了研究麻醉剂对TdP诱导性的影响,在戊巴比妥钠、氟烷或异氟烷麻醉下,对犬进行累积静脉注射奎尼丁前后,通过程控电刺激(PES)诱发心律失常。QTc延长和TdP发生率在氟烷麻醉的犬中最高,在给予戊巴比妥钠的犬中最低,这表明氟烷是该TdP模型最合适的麻醉剂。为了进一步验证该模型,在氟烷麻醉下对其他犬静脉注射阿司咪唑。0.3mg/kg的阿司咪唑使QT间期稍有延长,但未诱发任何心律失常。然而,在1mg/kg时,10只动物中有5只诱发了TdP,在3mg/kg时又有另外2只动物诱发了TdP。TdP诱发前出现单个和多个异位搏动,且异位搏动呈剂量依赖性。发生TdP的犬的奎尼丁血浆浓度等于或低于发生TdP的人的奎尼丁水平,而犬的阿司咪唑血浆浓度较高。总之,这种采用氟烷麻醉、完全性房室传导阻滞、PES以及同时测量血浆药物浓度的急性犬TdP模型,对于评估药物尤其是I(Kr)阻滞剂在人类中诱发TdP的风险具有重要价值。

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