Maurer Hans H, Sauer Christoph, Theobald Denis S
Department of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, University of Saarland, D-66421 Homburg (Saar), Germany.
Ther Drug Monit. 2006 Jun;28(3):447-53. doi: 10.1097/01.ftd.0000211812.27558.6e.
This review summarizes the major metabolic pathways of the drugs of abuse, tetrahydrocannabinol, cocaine, heroin, morphine, and codeine, in humans including the involvement of isoenzymes. This knowledge may be important for predicting their possible interactions with other xenobiotics, understanding pharmaco-/toxicokinetic and pharmacogenetic variations, toxicological risk assessment, developing suitable toxicological analysis procedures, and finally for understanding certain pitfalls in drug testing. The detection times of these drugs and/or their metabolites in biological samples are summarized and the implications of the presented data on the possible interactions of drugs of abuse with other xenobiotics, ie, inhibition or induction of individual polymorphic and nonpolymorphic isoenzymes, discussed.
本综述总结了人类滥用药物(四氢大麻酚、可卡因、海洛因、吗啡和可待因)的主要代谢途径,包括同工酶的参与情况。这些知识对于预测它们与其他外源化学物可能的相互作用、理解药代动力学/毒代动力学及药物遗传学变异、进行毒理学风险评估、开发合适的毒理学分析程序,以及最终理解药物检测中的某些陷阱可能具有重要意义。文中总结了这些药物及其代谢物在生物样品中的检测时间,并讨论了所呈现的数据对于滥用药物与其他外源化学物可能相互作用的影响,即对个体多态性和非多态性同工酶的抑制或诱导作用。