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环孢素与地尔硫䓬之间的药代动力学相互作用。

Pharmacokinetic interaction between cyclosporin and diltiazem.

作者信息

Brockmöller J, Neumayer H H, Wagner K, Weber W, Heinemeyer G, Kewitz H, Roots I

机构信息

Institute of Clinical Pharmacology, Freie Universität Berlin, FRG.

出版信息

Eur J Clin Pharmacol. 1990;38(3):237-42. doi: 10.1007/BF00315023.

Abstract

Previous reports have indicated that administration of the calcium antagonist diltiazem results in major changes in the pharmacokinetics of cyclosporin A (CyA). A new clinical trial was undertaken in 22 renal transplant patients receiving a constant dose of cyclosporin to further explore this interaction. Coadministration of diltiazem for one week produced an increase in the blood concentration of CyA and its metabolites 17 and 18 in almost all patients, but no increase in CyA metabolites 1 and 21. The mean whole blood CyA trough level determined by HPLC rose from 117 ng.ml-1 to 170 ng.ml-1 after one week on diltiazem, and the mean trough level of metabolite 17 rose similarly from 184 ng.ml-1 before to 336 ng.ml-1. Based on experiments with microsomes from human liver the effect of diltiazem was due to noncompetitive inhibition of CyA-metabolism by diltiazem, and the increased concentration of metabolite 17 might have been due to stronger inhibition of its secondary metabolism steps.

摘要

先前的报告表明,给予钙拮抗剂地尔硫䓬会导致环孢素A(CyA)的药代动力学发生重大变化。在22名接受恒定剂量环孢素的肾移植患者中进行了一项新的临床试验,以进一步探究这种相互作用。地尔硫䓬联合用药一周后,几乎所有患者的CyA及其代谢物17和18的血药浓度均升高,但CyA代谢物1和21未升高。通过高效液相色谱法测定,服用地尔硫䓬一周后,全血CyA的平均谷浓度从117 ng.ml-1升至170 ng.ml-1,代谢物17的平均谷浓度也类似地从之前的184 ng.ml-1升至336 ng.ml-1。基于用人肝微粒体进行的实验,地尔硫䓬的作用是由于其对CyA代谢的非竞争性抑制,代谢物17浓度的升高可能是由于其二级代谢步骤受到更强抑制。

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