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长期给予苯巴比妥对酚红肝胆转运的影响:通过统计矩分析进行评估。

Effect of chronic administration of phenobarbital on the hepatobiliary transport of phenol red: assessment by statistical moment analysis.

作者信息

Kakutani T, Endo K, Nara E, Nakazora S, Hashida M

机构信息

Faculty of Pharmaceutical Sciences, Kyoto University, Japan.

出版信息

Pharm Res. 1992 Jul;9(7):908-14. doi: 10.1023/a:1015852916524.

Abstract

The effect of enzyme induction on the hepatobiliary transport of phenol red (PR) in rats was investigated by application of a new analytical system to determine local drug disposition based on statistical moment theory (T. Kakutani et al., J. Pharmacokin. Biopharm. 13:609-631, 1985). Employing the moment parameters obtained from the time courses of plasma and biliary concentrations of PR and its metabolite after intravenous injection, the hepatobiliary transport of PR was theoretically assessed by separating it into component subprocesses such as hepatic uptake, hepatobiliary transfer, and intrahepatic metabolism. The results demonstrated that the acceleration of plasma disappearance of PR caused by pretreatment with phenobarbital (PB), known to induce hepatic enzyme systems, could be attributed to elevation of both hepatic and extrahepatic clearances. While PB did cause bile flow elevation (choleresis) and increased metabolism, these effects were shown to make little contribution to accelerated plasma disappearance of PR, since it was shown that the hepatobiliary excretion of PR was rate-limited by the intrahepatic transfer process, which was unaffected by PB treatment. From the results of this study, this experimental/analysis methodology seems to be useful in obtaining detailed information about hepatobiliary transport of the drug from in vivo data.

摘要

通过应用一种基于统计矩理论的新型分析系统来测定局部药物处置情况,研究了酶诱导对大鼠中酚红(PR)肝胆转运的影响(T. Kakutani等人,《药代动力学与生物药剂学杂志》13:609 - 631,1985年)。利用静脉注射后PR及其代谢产物的血浆和胆汁浓度随时间变化过程获得的矩参数,通过将PR的肝胆转运分离为肝摄取、肝胆转运和肝内代谢等组成子过程,从理论上对其进行了评估。结果表明,已知可诱导肝酶系统的苯巴比妥(PB)预处理导致PR血浆消失加速,这可归因于肝清除率和肝外清除率的升高。虽然PB确实导致胆汁流量升高(利胆作用)和代谢增加,但这些作用对PR血浆消失加速的贡献很小,因为已表明PR的肝胆排泄受肝内转运过程的限速,而该过程不受PB处理的影响。从本研究结果来看,这种实验/分析方法似乎有助于从体内数据中获取有关药物肝胆转运的详细信息。

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