Faculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
J Pharm Sci. 2011 Jun;100(6):2469-81. doi: 10.1002/jps.22437. Epub 2010 Dec 23.
Block of I(Kr) is of major concern in drug safety. The objective of this study was to assess prolongation of cardiac repolarization during the combined use of two I(Kr) blockers when administered concomitantly or sequentially. (1) When isolated hearts from male guinea pigs were perfused concomitantly with two I(Kr) blockers, prolongation of monophasic action potential duration measured at 90% (MAPD(90)) was less than the summation of effects observed for each drug perfused alone. (2) In sequential administration, when ketoconazole or erythromycin was perfused first, they antagonized MAPD(90)-prolonging effects of domperidone. This effect was absent when domperidone or dofetilide was perfused first. Patch-clamp experiments confirmed that the order of sequential perfusion impacts the decrease in HERG tail amplitude. In conclusion, this study does not support the concept that potentiation of drug effects is observed during the combined administration of two I(Kr) blockers. Furthermore, order of administration of two I(Kr) blockers together may be an important factor in drug-induced long QT syndrome.
I(Kr) 阻断是药物安全性的主要关注点。本研究的目的是评估当两种 I(Kr) 阻断剂同时或序贯给药时,心脏复极的延长。(1)当同时灌流两种 I(Kr) 阻断剂时,雄性豚鼠离体心脏的单相动作电位时程(MAPD(90))延长小于单独灌流每种药物时观察到的效应总和。(2)在序贯给药时,酮康唑或红霉素首先灌流时,拮抗了多潘立酮的 MAPD(90)延长作用。当首先灌流多潘立酮或决奈达隆时,这种作用不存在。膜片钳实验证实,序贯灌流的顺序影响 HERG 尾波幅度的降低。总之,本研究不支持两种 I(Kr) 阻断剂同时给药时观察到药物效应增强的概念。此外,两种 I(Kr) 阻断剂联合给药的顺序可能是药物引起长 QT 综合征的一个重要因素。