Department of Therapeutics and Pharmacology, The Queen's University of Belfast.
J Psychopharmacol. 1995 Jan;9(2):143-9. doi: 10.1177/026988119500900209.
Fifteen healthy male volunteers received single doses of 100 mg immediate release remoxipride (IR), 150 mg controlled release remoxipride (CR), 50 mg chlorpromazine (CPZ), 2 mg lorazepam (LZ), and placebo in a randomised, five-period cross-over study. Both saccadic (SEM) and smooth pursuit eye movements (SPEM) as well as a battery of psychomotor performance tests were assessed at 1.5-h intervals over 9 h following drug administration. The areas under the response-time curves and the maximum effect during the study period were analysed by analysis of variance. The most consistent impairments were produced by LZ. The neuroleptics caused impairments to SEM, and tended to impair critical flicker fusion, continuous attention and both paced and unpaced versions of the digit-symbol substitution test as well as subjective measures of sedation. Only LZ impaired SPEM. Neither paced nor unpaced psychomotor tests distinguished between neuroleptics and benzodiazepines. The low therapeutic doses of IR and CR produced similar impairments to a sub-therapeutic dose of CPZ. Selectivity of pharmacological action does not appear to predict selectivity of effect on psychomotor function.
15 名健康男性志愿者接受了单剂量 100mg 即刻释放型罗美昔朋(IR)、150mg 控释型罗美昔朋(CR)、50mg 氯丙嗪(CPZ)、2mg 劳拉西泮(LZ)和安慰剂的随机、五周期交叉研究。在给药后 9 小时内,每隔 1.5 小时评估扫视(SEM)和平滑追踪眼球运动(SPEM)以及一系列运动表现测试。通过方差分析分析反应时间曲线下面积和研究期间的最大效应。LZ 产生的影响最一致。神经安定剂导致 SEM 受损,并且倾向于损害临界闪烁融合、连续注意力以及数字符号替代测试的有节奏和无节奏版本以及镇静的主观测量。只有 LZ 损害了 SPEM。有节奏和无节奏的精神运动测试都不能区分神经安定剂和苯二氮䓬类药物。IR 和 CR 的低治疗剂量与 CPZ 的亚治疗剂量产生类似的损伤。药理作用的选择性似乎不能预测对精神运动功能的影响的选择性。