文章基本信息

标题：Hepatic Extraction of Tacrolimus in Rats with Experimental Liver Diseases
本地全文：下载
作者：Hiroaki SASA ; Yukiya HASHIMOTO ; Takako SHIMIZU 等
期刊名称：Biological and Pharmaceutical Bulletin
印刷版ISSN：0918-6158
电子版ISSN：1347-5215
出版年度：1998
卷号：21
期号：6
页码：610-614
DOI：10.1248/bpb.21.610
出版社：The Pharmaceutical Society of Japan
摘要：Tacrolimus, an immunosuppressive agent, is metabolized mainly in the liver and has shown large intra- and interindividual pharmacokinetic variability. We investigated the effect of liver dysfunctions on the pharmacokinetics of tacrolimus in rats with experimental liver diseases. Experimental hepatic failure was induced by CCl₄-treatment or bile duct ligation. Tacrolimus (1 or 0.3 mg/kg) was administered intravenously or intraportally to the rats (n=5-6 per group), and blood samples were collected over a 240-min period. The tacrolimus concentrations in the blood were then measured by a high-performance liquid chromatography-enzyme immunoassay. In the normal rats, the hepatic extraction ratio of tacrolimus (E_H) was dose-independent, ranging from 0.566-0.598 at 0.3 and 1.0 mg/kg doses. The E_H were dose-dependent in the CCl₄-treated rats and in the bile duct-ligated rats : the E_H at 1.0 mg/kg dose were 0.158-0.170 and those at 0.3 mg/kg dose were 0.329-0.394. The intermediate E_H of tacrolimus suggested that the clearance of tacrolimus depends not only on hepatic intrinsic clearance but also on hepatic blood flow. The present pharmacokinetic study also suggested that the decrease of E_H and the dose-dependence of E_H contribute to the elevation of blood tacrolimus concentrations and to the large variability in the pharmacokinetics of tacrolimus after oral administration in hepatic dysfunctions.
关键词：tacrolimus;pharmacokinetics;hepatic extraction ratio;hepatic dysfunction