Department of Internal Medicine, Institute of Clinical Medicine, and Biocenter Oulu, University of Oulu, Oulu, Finland.
Expert Rev Clin Pharmacol. 2012 Sep;5(5):569-85. doi: 10.1586/ecp.12.39.
The induction of drug-metabolizing enzymes is a special case of pharmacokinetic interactions with consequences for the concurrent drug therapy. The most important enzymes affecting the pharmacokinetics of pharmaceuticals are cytochrome P450 (CYP) enzymes and their induction is often of utmost importance for the effects of the metabolized drugs. This review presents the current knowledge on the inducers of the specific CYP enzymes in humans. The focus is solely on human in vivo findings; in vitro results are referenced only when needed to interpret the induction mechanisms. As the mechanisms of CYP induction are important in understanding the effects of inducers, a concise overview of the various receptors affecting the induction of human CYP enzymes is presented.
药物代谢酶的诱导是一种特殊的药代动力学相互作用情况,会对同时进行的药物治疗产生影响。影响药物代谢动力学的最重要的酶是细胞色素 P450(CYP)酶,其诱导通常对代谢药物的作用至关重要。本文综述了目前关于人类特定 CYP 酶诱导剂的知识。本文仅关注人类体内的发现;仅在需要解释诱导机制时才参考体外结果。由于 CYP 诱导的机制对于理解诱导剂的作用很重要,因此本文简要概述了影响人类 CYP 酶诱导的各种受体。