Kuitunen T, Mattila M J, Seppala T
Department of Pharmacology, University of Helsinki, Finland.
Int Clin Psychopharmacol. 1990 Apr;5 Suppl 2:115-30.
Actions and interactions with ethanol (0.8 g/kg) of triazolam (TRZ, 0.25 mg) and zopiclone (ZOP, 7.5 mg) on performance and memory were studied with 12 healthy young subjects. The randomized double-blind and crossover test sessions were carried out at 1-week intervals. Each time a set of performance tests and self-assessments on visual analogue scales were done before the treatment and 1.5, 3, 4.5, 6 and 8 h after it. The clinical test for drunkenness (CTD) was done 2 and 5 h after drug intake. Venous blood was sampled after each set of tests. Both TRZ and ZOP impaired coordinative and reactive skills, but not peripheral attention or body balance. They also impaired cognitive test performance (digit substitution, symbol copying), and lowered flicker fusion threshold. The psychomotor effects of the two hypnotics and measures of subjective sedation peaked at 1.5 and 3 h. Spatial memory was impaired by TRZ at 4.5 h. Cognitive tests and tracking were most sensitive to alcohol. Furthermore alcohol impaired both motor and vestibular aspects of the CTD while both ZOP and TRZ alone had only minor effects. Alcohol enhanced and prolonged the effects of both hypnotics without modifying their plasma concentrations. Drug-alcohol interactions were mainly additive though more obvious with TRZ. Interactions were evident also on the CTD. The hypnotics were free from residual psychomotor and cognitive effects at 8 h even after the coadministration of alcohol. It is concluded that ZOP and TRZ have a mainly additive interaction with alcohol but pharmacokinetic mechanisms do not seem to contribute essentially to this.
以12名健康青年受试者为对象,研究了三唑仑(TRZ,0.25毫克)和佐匹克隆(ZOP,7.5毫克)与乙醇(0.8克/千克)对行为表现和记忆的作用及相互作用。随机双盲交叉试验在1周的间隔期进行。每次在治疗前以及治疗后1.5、3、4.5、6和8小时进行一组行为表现测试和视觉模拟量表的自我评估。在服药后2和5小时进行醉酒临床测试(CTD)。每组测试后采集静脉血样。TRZ和ZOP均损害协调和反应技能,但不影响外周注意力或身体平衡。它们还损害认知测试表现(数字替代、符号抄写),并降低闪烁融合阈值。两种催眠药的精神运动效应和主观镇静指标在1.5和3小时达到峰值。TRZ在4.5小时损害空间记忆。认知测试和追踪对酒精最为敏感。此外,酒精损害CTD的运动和前庭方面,而单独使用ZOP和TRZ只有轻微影响。酒精增强并延长了两种催眠药的作用,而不改变其血浆浓度。药物-酒精相互作用主要是相加性的,尽管TRZ的相互作用更明显。在CTD上也有明显的相互作用。即使在同时给予酒精后,催眠药在8小时时也没有残留的精神运动和认知效应。结论是,ZOP和TRZ与酒精主要存在相加性相互作用,但药代动力学机制似乎对此没有实质性贡献。