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联合使用红霉素会增加阿托伐他汀的血浆浓度。

Erythromycin coadministration increases plasma atorvastatin concentrations.

作者信息

Siedlik P H, Olson S C, Yang B B, Stern R H

机构信息

Department of Pharmacokinetics, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, Michigan 48105, USA.

出版信息

J Clin Pharmacol. 1999 May;39(5):501-4.

Abstract

The effect of erythromycin on the pharmacokinetics of atorvastatin, an inhibitor of HMG-CoA reductase, was investigated in 12 healthy volunteers. Each subject received a single 10 mg dose of atorvastatin on two separate occasions, separated by 2 weeks. Erythromycin (500 mg qid) was given from 7 days before through 4 days after the second atorvastatin dose. Atorvastatin concentrations were determined by an enzyme inhibition assay, which measured both atorvastatin and active metabolites. When erythromycin was coadministered with atorvastatin, mean Cmax and AUC(0-infinity) increased by 37.7% and 32.5%, respectively. Mean terminal half-life was similar following each atorvastatin dose. Possible mechanisms for this interaction include erythromycin inhibition of first-pass conversion of atorvastatin to inactive metabolites and erythromycin inhibition of P-glycoprotein-mediated intestinal or biliary secretion.

摘要

在12名健康志愿者中研究了红霉素对HMG-CoA还原酶抑制剂阿托伐他汀药代动力学的影响。每位受试者在两个不同的时间点分别接受单次10mg剂量的阿托伐他汀,间隔2周。从第二次阿托伐他汀给药前7天至给药后4天给予红霉素(500mg,每日4次)。通过酶抑制试验测定阿托伐他汀浓度,该试验可同时测定阿托伐他汀及其活性代谢物。当红霉素与阿托伐他汀合用时,平均Cmax和AUC(0-∞)分别增加了37.7%和32.5%。每次阿托伐他汀给药后的平均终末半衰期相似。这种相互作用的可能机制包括红霉素抑制阿托伐他汀首过转化为无活性代谢物以及红霉素抑制P-糖蛋白介导的肠道或胆汁分泌。

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