Patrick Kennerly S, Straughn Arthur B, Reeves Owen T, Bernstein Hilary, Malcolm Robert
From the *Department of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, SC; †Department of Pharmaceutical Sciences, University of Tennessee Health Sciences Center, Memphis, TN; and ‡Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC.
J Clin Psychopharmacol. 2015 Aug;35(4):464-7. doi: 10.1097/JCP.0000000000000348.
The potentiation of positive subjective responses to immediate-release dexmethylphenidate (d-MPH) or dl-methylphenidate (dl-MPH) by ethanol was investigated over the time course of maximal drug exposure after a single dose. In a 4-way, randomized, crossover study design, 12 men and 12 women normal volunteers received d-MPH (0.15 mg/kg) or dl-MPH (0.3 mg/kg) with or without ethanol (0.6 g/kg). Serial visual analog scales were used as surrogates for drug abuse liability ("high," "good," "like," "stimulated," and "any drug effect"). Combining pure d-MPH with ethanol significantly (P < 0.005) increased the area under the effect curves (AUC(0-5.25h)) of all 5 subscales. The dl-MPH-ethanol combination significantly (P < 0.05) increased these AUCs with the exception of like (P = 0.08). Effects of the pure d-MPH-ethanol combination exhibited delayed potentiation relative to dl-MPH-ethanol. A pharmacokinetic interaction between the l-isomer of dl-MPH and ethanol has previously been shown to increase early exposure to d-MPH. Administration of the pure isomer d-MPH precludes this absorption phase pharmacokinetic interaction with ethanol. This notwithstanding, the pure d-MPH-ethanol combination resulted in comparable, if not greater, cumulative stimulant potentiation than the dl-MPH-ethanol combination. These findings provide evidence of a pharmacodynamic component to d-MPH-ethanol synergistic interactions and carry implications for the rational drug individualization in the treatment of attention-deficit/hyperactivity disorder.
在单次给药后最大药物暴露的时间进程中,研究了乙醇对速释右哌甲酯(d-MPH)或消旋哌甲酯(dl-MPH)阳性主观反应的增强作用。在一项4组随机交叉研究设计中,12名男性和12名女性正常志愿者接受d-MPH(0.15 mg/kg)或dl-MPH(0.3 mg/kg),同时给予或不给予乙醇(0.6 g/kg)。采用系列视觉模拟量表作为药物滥用倾向(“兴奋”、“良好”、“喜欢”、“兴奋感”和“任何药物效应”)的替代指标。将纯d-MPH与乙醇联合使用显著(P < 0.005)增加了所有5个分量表的效应曲线下面积(AUC(0 - 5.25h))。dl-MPH与乙醇联合使用显著(P < 0.05)增加了这些AUC,但“喜欢”分量表除外(P = 0.08)。与dl-MPH-乙醇组合相比,纯d-MPH-乙醇组合的效应表现出延迟增强。先前已证明dl-MPH的l-异构体与乙醇之间存在药代动力学相互作用,可增加早期d-MPH暴露。给予纯异构体d-MPH可避免这种与乙醇的吸收相药代动力学相互作用。尽管如此,纯d-MPH-乙醇组合产生的累积兴奋增强作用与dl-MPH-乙醇组合相当,甚至更大。这些发现为d-MPH-乙醇协同相互作用中的药效学成分提供了证据,并对注意力缺陷/多动障碍治疗中的合理药物个体化具有启示意义。