Tata N V, Subbotina N, Burckart G, Swaminathan A, Gusev A I, Hercules D M, Venkataramanan R
School of Pharmacy, University of Pittsburgh, PA 15261, USA.
Res Commun Mol Pathol Pharmacol. 1997 Apr;96(1):107-10.
The in vitro metabolism of tacrolimus (TAC, FK 506) was investigated in the liver microsomes prepared from normal rats as well as rats treated with dexamethasone (DEX) and rifampin (RIF). The rate of tacrolimus metabolism was similar in control and RIF treated rat liver microsomes, whereas it significantly increased in microsomes obtained from dexamethasone treated rats. Seven different possible metabolites were identified in the microsomal preparations from rats treated with rifampin or dexamethasone whereas the microsomes from the control rats failed to produce the mono-demethylated and monohydroxylated metabolite of TAC (TAC+2, m/z = 805.5). There was an apparent difference in the amount of individual metabolites formed in different groups. This indicates quantitative differences in the induction of cytochrome P450 3A, an enzyme sub family known to be primarily responsible for tacrolimus metabolism. Lack of induction of tacrolimus metabolism by rifampin can be attributed to the lack of effect of rifampin in inducing cytochrome P450 3A in rats.
在从正常大鼠以及用 dexamethasone(DEX)和 rifampin(RIF)处理过的大鼠制备的肝微粒体中研究了他克莫司(TAC,FK 506)的体外代谢。在对照和 RIF 处理的大鼠肝微粒体中,他克莫司的代谢速率相似,而在地塞米松处理的大鼠获得的微粒体中其代谢速率显著增加。在用利福平或地塞米松处理的大鼠的微粒体制剂中鉴定出七种不同的可能代谢物,而对照大鼠的微粒体未能产生 TAC 的单去甲基化和单羟基化代谢物(TAC+2,m/z = 805.5)。不同组中形成的各个代谢物的量存在明显差异。这表明细胞色素 P450 3A 诱导的定量差异,细胞色素 PZ50 3A 是已知主要负责他克莫司代谢的一个酶亚家族。利福平对他克莫司代谢缺乏诱导作用可归因于利福平对大鼠细胞色素 P450 3A 诱导缺乏作用。