Lane E A, Guthrie S, Linnoila M
Clin Pharmacokinet. 1985 May-Jun;10(3):228-47. doi: 10.2165/00003088-198510030-00003.
Pharmacokinetic interactions of ethanol with other drugs, including its effects upon drug metabolite disposition, are reviewed in terms of clearance concepts. This approach is particularly useful in understanding the mechanisms of ethanol-drug interactions, i.e. in separating the effects of ethanol upon drug clearance, volume of distribution and plasma protein binding. The application of clearance concepts provides the basis for understanding the qualitative differences in ethanol interactions with low and high hepatic extraction ratio drugs. The effects of short and long term ethanol consumption upon different types of drug metabolism (oxidative, acetylation and glucuronidation) have been considered. Long term ethanol consumption may increase the clearance of a drug by induction of oxidative metabolism whereas short term consumption may decrease the clearance of such a drug. Clearance by N-acetylation appears to be increased in the presence of ethanol, and clearance by conjugation to glucuronic acid is decreased for some drugs by single-dose consumption of ethanol.
从清除率概念的角度综述了乙醇与其他药物的药代动力学相互作用,包括其对药物代谢产物处置的影响。这种方法在理解乙醇 - 药物相互作用机制方面特别有用,即用于区分乙醇对药物清除率、分布容积和血浆蛋白结合的影响。清除率概念的应用为理解乙醇与高、低肝提取率药物相互作用的定性差异提供了基础。还考虑了短期和长期乙醇摄入对不同类型药物代谢(氧化、乙酰化和葡萄糖醛酸化)的影响。长期乙醇摄入可能通过诱导氧化代谢增加药物清除率,而短期摄入可能降低此类药物的清除率。在乙醇存在的情况下,N - 乙酰化清除率似乎会增加,而单次摄入乙醇会使某些药物与葡萄糖醛酸结合的清除率降低。