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利用慢性房室传导阻滞食蟹猴作为体内模型评估药物相互作用相关尖端扭转型室性心动过速。

Utilization of the chronic atrioventricular block cynomolgus monkey as an in vivo model to evaluate drug interaction-associated torsade de pointes.

机构信息

Department of Pharmacology, Toho University Graduate School of Medicine, 5-21-16 Omori-nishi, Ota-ku, Tokyo, 143-8540, Japan.

Ina Research Inc., 2148-188 Nishiminowa, Ina-shi, Nagano, 399-4501, Japan.

出版信息

J Pharmacol Sci. 2020 Apr;142(4):172-175. doi: 10.1016/j.jphs.2019.12.007. Epub 2020 Jan 7.

Abstract

It has been difficult to experimentally reproduce synergistic effects of ketoconazole on terfenadine-induced torsade de pointes. We assessed proarrhythmic effects of terfenadine (30 mg/kg, p.o.) with/without ketoconazole (100 mg/kg, p.o.) pretreatment using the chronic atrioventricular block cynomolgus monkeys with repeated-measured design (n = 4). Terfenadine with ketoconazole pretreatment repeatedly induced non-sustained torsade de pointes in each animal, although terfenadine alone did not induce it at all. Thus, the chronic atrioventricular block cynomolgus monkeys can be used for studying drug interaction-associated torsade de pointes, providing a non-clinical strategy to circumvent untoward drug interactions in patients specially under polypharmacy.

摘要

实验重现酮康唑增强特非那定致尖端扭转型室性心动过速的协同作用一直存在困难。我们采用重复测量设计(n=4),利用慢性房室传导阻滞食蟹猴评估特非那定(30mg/kg,po)联合/不联合酮康唑(100mg/kg,po)预处理的致心律失常作用。虽然特非那定单用根本不会诱发,但酮康唑预处理后特非那定可反复诱发非持续尖端扭转型室性心动过速。因此,慢性房室传导阻滞食蟹猴可用于研究药物相互作用相关尖端扭转型室性心动过速,为避免多药治疗患者出现不良药物相互作用提供一种非临床策略。

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