Kroboth P D, McAuley J W, Derry C L
Department of Pharmacy and Therapeutics, University of Pittsburgh, Pennsylvania, 15261, USA.
J Clin Psychopharmacol. 1995 Jun;15(3):192-6. doi: 10.1097/00004714-199506000-00007.
Evidence of time-dependent sensitization (TDS) to triazolam was observed in three separate clinical studies. Study 1 was conducted in 12 normal-weight and 12 obese men; an intravenous bolus dose of triazolam, 0.5 mg, was administered on two occasions. Study 2 was a balanced crossover of three 0.25-mg oral doses and one 0.20-mg oral dose of triazolam in 11 men. Study 3 was a balanced crossover of one placebo, one 0.5-mg, and two 0.4-mg oral doses of triazolam. In all three studies, treatments were separated by 6 days and included serial blood sampling for characterization of pharmacokinetics. Psychomotor response was assessed with the Digit Symbol Substitution Test and the Continuous Performance Test (CPT). Sedation was rated by an observer. For each measure, an effect ratio was calculated as the area under the effect curve divided by the area under the triazolam concentration curve; this parameter relates the extent of response relative to drug concentration in plasma. Effect ratios increased progressively by week for CPT; the percentage increase ranged from 31.9% in the study 1 normal subjects (week 1 to week 2; p = 0.08) to 631% in study 2 (week 1 to week 4; p = 0.0013). Similar increases were observed for other responses. Overall, the effect ratio data demonstrate increasing responsiveness per unit of triazolam concentration when triazolam was administered as a single dose at 1-week intervals. This observation was incidental to the original objectives of the studies. However, the data suggest that definitive studies to verify the occurrence of this phenomenon need to be conducted.(ABSTRACT TRUNCATED AT 250 WORDS)
在三项独立的临床研究中观察到了对三唑仑的时间依赖性致敏(TDS)证据。研究1对12名体重正常的男性和12名肥胖男性进行;分两次静脉推注0.5毫克三唑仑。研究2是11名男性中三种0.25毫克口服剂量和一种0.20毫克口服剂量三唑仑的平衡交叉试验。研究3是一种安慰剂、一种0.5毫克和两种0.4毫克口服剂量三唑仑的平衡交叉试验。在所有三项研究中,治疗间隔为6天,包括进行系列血样采集以表征药代动力学。通过数字符号替换测试和连续性能测试(CPT)评估精神运动反应。由一名观察者对镇静程度进行评分。对于每项测量,计算效应比,即效应曲线下面积除以三唑仑浓度曲线下面积;该参数将反应程度与血浆中药物浓度相关联。CPT的效应比逐周逐渐增加;增加百分比范围从研究1正常受试者中的31.9%(第1周与第2周;p = 0.08)到研究2中的631%(第1周与第4周;p = 0.0013)。其他反应也观察到类似增加。总体而言,当三唑仑以1周的间隔作为单剂量给药时,效应比数据表明每单位三唑仑浓度的反应性增加。这一观察结果是这些研究最初目标之外的偶然发现。然而,数据表明需要进行确定性研究以验证这一现象的发生。(摘要截于250字)