Ekstrøm P O, Giercksky K E, Andersen A, Slørdal L
Department of Surgical Oncology, The Norwegian Radium Hospital, Oslo.
Life Sci. 1997;60(24):PL 359-64. doi: 10.1016/s0024-3205(97)00241-5.
Reports of a potentially life-threatening interaction between the antifolate methotrexate (MTX) and drugs belonging to the NSAID class instigated a study of MTX pharmacokinetics by a microdialysis technique in the presence and absence of the NSAID naproxen in anesthetized rats. After pretreatment with naproxen, the animals received either 750 or 1,000 mg/kg MTX as a 6 h continuous intravenous infusion. During infusions, microdialysis effluents were obtained from probes situated intravenously, intrahepatically and intrarenally. In all three compartments, time-concentration AUCs for both MTX and its major extracellular metabolite, 7-hydroxymethotrexate (7-OH-MTX), increased about two-fold in the presence of naproxen. The mechanisms responsible for the MTX-NSAID interaction are briefly discussed. The study demonstrate that the microdialysis technique offers a means to investigate pharmacokinetic drug-drug interactions.
有报告称,抗叶酸药物甲氨蝶呤(MTX)与非甾体抗炎药(NSAID)类药物之间可能存在危及生命的相互作用,这促使人们采用微透析技术,在麻醉大鼠体内存在和不存在非甾体抗炎药萘普生的情况下,对MTX的药代动力学进行研究。在用萘普生预处理后,动物接受750或1000 mg/kg的MTX,持续静脉输注6小时。在输注过程中,从静脉内、肝内和肾内的探针获取微透析流出液。在所有三个隔室中,在存在萘普生的情况下,MTX及其主要细胞外代谢物7-羟基甲氨蝶呤(7-OH-MTX)的时间-浓度曲线下面积(AUC)增加了约两倍。文中简要讨论了MTX与NSAID相互作用的机制。该研究表明,微透析技术为研究药代动力学药物-药物相互作用提供了一种手段。