Turner P V, Renton K W
Department of Pharmacology, Dalhousie University, Halifax, N.S., Canada.
Can J Physiol Pharmacol. 1989 Jun;67(6):582-6. doi: 10.1139/y89-093.
Erythromycin has been reported to interact with the anticonvulsant, carbamazepine, in both children and adults. Toxic serum levels of carbamazepine are observed within 24 h of antibiotic administration, suggesting a mechanism not previously described for other erythromycin-based drug interactions. In rats erythromycin significantly depressed the elimination of carbamazepine in animals induced with carbamazepine for 4 days but had no effect on carbamazepine elimination in noninduced animals. Although the in vitro metabolism of carbamazepine to its epoxide by hepatic microsomes prepared from noninduced rats was significantly inhibited by erythromycin, the inhibition of carbamazepine epoxidation was greatly enhanced in carbamazepine-induced rats. In the pig the sensitivity of carbamazepine metabolism to erythromycin was much greater than in the rat, indicating the existence of a large species difference in this particular drug interaction. It is concluded that the interaction between erythromycin and carbamazepine is caused by a direct inhibition of carbamazepine oxidation by the antibiotic.
据报道,红霉素在儿童和成人中均会与抗惊厥药卡马西平发生相互作用。在使用抗生素后的24小时内可观察到卡马西平的血清中毒水平,这表明存在一种此前未描述过的基于红霉素的药物相互作用机制。在大鼠中,红霉素显著降低了连续4天服用卡马西平的动物体内卡马西平的消除率,但对未诱导动物的卡马西平消除没有影响。尽管红霉素可显著抑制由未诱导大鼠制备的肝微粒体将卡马西平体外代谢为其环氧化物,但在卡马西平诱导的大鼠中,对卡马西平环氧化的抑制作用大大增强。在猪中,卡马西平代谢对红霉素的敏感性远高于大鼠,表明在这种特定的药物相互作用中存在很大的物种差异。得出的结论是,红霉素与卡马西平之间的相互作用是由抗生素直接抑制卡马西平氧化所致。