Luurila H, Olkkola K T, Neuvonen P J
Department of Clinical Pharmacology, University of Helsinki, Finland.
Pharmacol Toxicol. 1995 Apr;76(4):255-8. doi: 10.1111/j.1600-0773.1995.tb00139.x.
Interaction between erythromycin, a strong inhibitor of CYP3A4, and nitrazepam, a long-acting benzodiazepine, was investigated in a double-blind and randomized cross-over study of two phases. Ten healthy volunteers received erythromycin (500 mg x 3) orally or placebo for 6 days. On the fourth day they were given a challenge dose of 5 mg nitrazepam. Plasma samples were collected and psychomotor effects were measured during 42 hr after intake of nitrazepam. There was a statistically significant pharmacokinetic interaction between erythromycin and nitrazepam. Erythromycin increased the area under the nitrazepam concentration-time curve by 25% (P < 0.05) and the peak concentration by 30% (P < 0.05). The concentration peak time of nitrazepam was shortened by over 50% (P < 0.05). The elimination half-lives did not change. Accordingly, as far as the metabolism of nitrazepam is concerned, erythromycin does not cause any major changes in the metabolism of nitrazepam. In psychomotor performance only minor differences were seen. It is concluded that the interaction between erythromycin and nitrazepam is of little clinical significance.
在一项分两个阶段的双盲随机交叉研究中,对强效CYP3A4抑制剂红霉素与长效苯二氮䓬类药物硝西泮之间的相互作用进行了研究。10名健康志愿者口服红霉素(500毫克×3次)或安慰剂,为期6天。在第4天,给他们服用5毫克硝西泮的激发剂量。采集血浆样本,并在服用硝西泮后的42小时内测量精神运动效应。红霉素与硝西泮之间存在具有统计学意义的药代动力学相互作用。红霉素使硝西泮浓度-时间曲线下面积增加25%(P<0.05),使峰值浓度增加30%(P<0.05)。硝西泮的浓度达峰时间缩短超过50%(P<0.05)。消除半衰期未改变。因此,就硝西泮的代谢而言,红霉素不会引起硝西泮代谢的任何重大变化。在精神运动表现方面,仅观察到微小差异。得出的结论是,红霉素与硝西泮之间的相互作用临床意义不大。