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他汀类药物的药物相互作用。

Drug interactions with statins.

出版信息

Acta Pharm. 2013 Sep;63(3):277-93. doi: 10.2478/acph-2013-0022.

Abstract

The 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) are generally well tolerated as monotherapy. Statins are associated with two important adverse effects, asymptomatic elevation in liver enzymes and myopathy. Myopathy is most likely to occur when statins are administered with other drugs. Statins are substrates of multiple drug transporters (including OAT- -P1B1, BCRP and MDR1) and several cytochrome P450 (CYP) enzymes (including CYP3A4, CYP2C8, CYP2C19, and CYP2C9). Possible adverse effects of statins can occur due to interactions in concomitant use of drugs that substantially inhibit or induce their methabolic pathway. This review summarizes the most important interactions of statins.

摘要

3-羟基-3-甲基戊二酰辅酶 A(HMG-CoA)还原酶抑制剂(他汀类药物)作为单一疗法通常具有良好的耐受性。他汀类药物与两种重要的不良反应有关,即无症状的肝酶升高和肌病。当他汀类药物与其他药物联合使用时,最有可能发生肌病。他汀类药物是多种药物转运体(包括 OAT-P1B1、BCRP 和 MDR1)和几种细胞色素 P450(CYP)酶(包括 CYP3A4、CYP2C8、CYP2C19 和 CYP2C9)的底物。由于同时使用的药物在很大程度上抑制或诱导其代谢途径,他汀类药物可能会发生不良反应。本文综述了他汀类药物最重要的相互作用。

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