Okamoto M, Rao S N, Aaronson L M, Walewski J L
Alcohol Clin Exp Res. 1985 Dec;9(6):516-21. doi: 10.1111/j.1530-0277.1985.tb05595.x.
Drug interactions between ethanol and pentobarbital and ethanol and chlordiazepoxide were investigated utilizing mice. At the peak of oral ethanol (0-4 g/kg), either sodium pentobarbital (1-120 mg/kg) or chlordiazepoxide hydrochloride (2-400 mg/kg) was given intraperitoneally. Blood concentrations of ethanol, pentobarbital, chlordiazepoxide, and its pharmacologically active major metabolites were monitored utilizing either gas chromatography or high performance liquid chromatography. Lethality and loss-of-righting reflex were measured as indexes of behavioral drug interactions. It was evident from the isobolographic plot that the interactions between ethanol and pentobarbital and ethanol and chlordiazepoxide were more than additive. Interaction between ethanol and pentobarbital was greater than that between ethanol and chlordiazepoxide. Furthermore, with increasing ethanol pretreatment the shift in dose-response curves for the loss-of-righting reflex was affected more than the shift in dose-response curves for lethality. Blood concentration monitoring of each drug indicated that the rate of biotransformation of pentobarbital was significantly decreased; sequential biotransformation of chlordiazepoxide was also altered, resulting in a large accumulation of demethylchlordiazepoxide in the blood.
利用小鼠研究了乙醇与戊巴比妥以及乙醇与氯氮卓之间的药物相互作用。在口服乙醇(0 - 4 g/kg)达到峰值时,腹腔注射戊巴比妥钠(1 - 120 mg/kg)或盐酸氯氮卓(2 - 400 mg/kg)。利用气相色谱法或高效液相色谱法监测乙醇、戊巴比妥、氯氮卓及其药理活性主要代谢物的血药浓度。测量致死率和翻正反射消失作为行为药物相互作用的指标。从等效应线图可以明显看出,乙醇与戊巴比妥以及乙醇与氯氮卓之间的相互作用大于相加作用。乙醇与戊巴比妥之间的相互作用大于乙醇与氯氮卓之间的相互作用。此外,随着乙醇预处理剂量的增加,翻正反射消失的剂量反应曲线的偏移比致死率剂量反应曲线的偏移受到的影响更大。每种药物的血药浓度监测表明,戊巴比妥的生物转化速率显著降低;氯氮卓的顺序生物转化也发生改变,导致去甲基氯氮卓在血液中大量蓄积。