Cohen A F, Ashby L, Crowley D, Land G, Peck A W, Miller A A
Br J Clin Pharmacol. 1985 Dec;20(6):619-29. doi: 10.1111/j.1365-2125.1985.tb05120.x.
Twelve healthy male volunteers received phenytoin 0.5 and 1 g, lamotrigine (a new anticonvulsant) 120 and 240 mg, diazepam 10 mg and placebo orally in a double-blind, cross-over, randomized trial. Maximum drug concentrations at 4 h, measured in plasma were 11.5 +/- 2.2 micrograms ml-1 for phenytoin and 2.7 +/- 0.4 micrograms ml-1 for lamotrigine. These levels were in the therapeutic range for phenytoin and the putative therapeutic range for lamotrigine. Side effects after diazepam (mainly sedation) and phenytoin (mainly unsteadiness) differed markedly from lamotrigine which produced no important side effects. Subjective effects as measured by visual analogue scales were caused by phenytoin and diazepam but not by lamotrigine. Diazepam impaired eye movements, adaptive tracking and body sway. Phenytoin impaired adaptive tracking, increased body sway and impaired smooth pursuit eye movement. Lamotrigine produced only a possible slight increase in body sway. There were significant correlations between performance and saliva levels of phenytoin and diazepam. It was concluded that the tests used were suitable for monitoring CNS effects of anticonvulsants and that lamotrigine possibly could have a more favourable CNS side effect profile than phenytoin.
在一项双盲、交叉、随机试验中,12名健康男性志愿者口服了0.5克和1克苯妥英、120毫克和240毫克拉莫三嗪(一种新型抗惊厥药)、10毫克地西泮以及安慰剂。血浆中4小时测得的苯妥英最大药物浓度为11.5±2.2微克/毫升,拉莫三嗪为2.7±0.4微克/毫升。这些水平处于苯妥英的治疗范围内以及拉莫三嗪的假定治疗范围内。地西泮(主要是镇静作用)和苯妥英(主要是步态不稳)后的副作用与拉莫三嗪明显不同,拉莫三嗪未产生重要副作用。通过视觉模拟量表测量的主观效应由苯妥英和地西泮引起,而非拉莫三嗪。地西泮损害眼球运动、适应性跟踪和身体摆动。苯妥英损害适应性跟踪、增加身体摆动并损害平稳跟踪眼球运动。拉莫三嗪仅可能使身体摆动略有增加。苯妥英和地西泮的表现与唾液水平之间存在显著相关性。得出的结论是,所使用的测试适用于监测抗惊厥药的中枢神经系统效应,并且拉莫三嗪可能比苯妥英具有更有利的中枢神经系统副作用谱。