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No effect of short-term omeprazole intake on acenocoumarol pharmacokinetics and pharmacodynamics

机译:短期摄入奥美拉唑对乙酰香豆酚的药代动力学和药效学没有影响

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摘要

> Aims To investigate the effect of omeprazole on the pharmacokinetics of R- and S-acenocoumarol and on their combined anticoagulant activity. > Methods Eight healthy male subjects completed a double-blind, randomized, placebo-controlled, two-way cross-over study. Subjects were given either omeprazole 40 mg or placebo once daily for 3 days. On day 2 of each study period, a single 10 mg oral dose of racemic acenocoumarol was administered and venous blood samples were collected for pharmacokinetic and pharmacodynamic assessments. A wash-out period of 2 weeks separated the two study periods. > Results The pharmacokinetics of R- and S-acenocoumarol (AUC 3016±221 and 233±14 ng ml−1 h, respectively) did not change after omeprazole (AUC 2929±256 and 220±18 ng ml−1 h, respectively). Anticoagulant activity (INRmax 1.7±0.1) was unaffected by co-administration of omeprazole (INRmax 1.7±0.1). > Conclusions The short-term intake of omeprazole does not affect acenocoumarol pharmacokinetics or pharmacodynamics. These data differ from the results of previous studies on the effect of omeprazole on warfarin, suggesting a different in vivo interaction profile of omeprazole on acenocoumarol than on warfarin. Drug interaction studies with oral anticoagulants should not be restricted to the use of warfarin.
机译:> 目的:研究奥美拉唑对R-和S-乙酰香豆酚的药代动力学及其联合抗凝活性的影响。 > 方法:八名健康的男性受试者完成了一项双盲,随机,安慰剂对照,双向交叉研究。每天一次给受试者服用奥美拉唑40mg或安慰剂,持续3天。在每个研究期的第2天,口服单剂量10μmg消旋乙酰香豆酚,并收集静脉血样本进行药代动力学和药效学评估。 2周的淘汰期将两个研究期分开。 > 结果:奥美拉唑(AUC 2929±)后,R-和S-乙酰香豆酚(分别为AUC 3016±221和233±14μngml -1 h)的药代动力学没有变化。分别为256和220±18 ng ml -1 h)。抗凝活性(INRmax 1.7±0.1)不受奥美拉唑(INRmax 1.7±0.1)的共同给药的影响。 > 结论:短期摄入奥美拉唑不会影响乙酰香豆酚的药代动力学或药效学。这些数据与先前关于奥美拉唑对华法林的作用的研究结果不同,表明奥美拉唑对乙酰香豆酚的体内相互作用与对华法林的相互作用不同。口服抗凝药的药物相互作用研究不应局限于使用华法林。

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