Davis M P, Homsi J
Harry R. Horvitz Center for Palliative Medicine, Cleveland Clinic Foundation, OH 44195, USA.
Support Care Cancer. 2001 Sep;9(6):442-51. doi: 10.1007/s005200000222.
The enzymes in the cytochrome p450 monooxygenase system (CYP) are the major enzymes responsible for metabolizing medications. The CYP2D6 isomer is responsible for metabolizing certain opioids, neuroleptics, antidepressants and cardiac medications. Owing to CYP2D6's low capacity and high affinity it is easily saturated by substrate and/or inhibited, resulting in pharmacokinetic interactions. Polymorphisms of the structural gene are common, leading to wide inter-individual and ethnic differences in drug metabolism. Clinically important drug interactions, which may be anticipated in the palliative medicine population, are reviewed.
细胞色素P450单加氧酶系统(CYP)中的酶是负责药物代谢的主要酶。CYP2D6异构体负责某些阿片类药物、抗精神病药物、抗抑郁药物和心脏药物的代谢。由于CYP2D6的低容量和高亲和力,它很容易被底物饱和和/或受到抑制,从而导致药代动力学相互作用。结构基因的多态性很常见,导致个体间和种族间在药物代谢方面存在很大差异。本文综述了在姑息治疗人群中可能出现的具有临床重要性的药物相互作用。