Kirk T, Roache J D, Griffiths R R
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Clin Psychopharmacol. 1990 Jun;10(3):160-7.
The effects of placebo, triazolam (0.25, 0.5, and 0.75 mg), and pentobarbital (100, 200, and 300 mg) were examined in seven normal male volunteers using a double-blind, Latin Square, balanced crossover design. Before and at hourly intervals after oral drug administration at approximately 10 a.m., subjects completed subject ratings of drug effects, psychomotor performance tasks, and two versions of a number recall task in which eight-digit number stimuli were recalled by reproduction on a numeric keypad. In one version, number stimuli were displayed on a video screen for varying lengths of time (3, 6, or 9 seconds) before immediate recall. In another version, subjects initially reproduced a continuously displayed number and then recalled the number following an immediate or a 16-second delay interval. Both triazolam and pentobarbital produced dose-related effects on all measures. Relative potency comparisons showed that triazolam was 270-384 times more potent than pentobarbital on subject ratings and psychomotor measures but was 406-647 times more potent than pentobarbital on measures of recall impairment. Recall performance deficits produced by both triazolam and pentobarbital at short (3-second) stimulus presentation times were attenuated at longer presentation times. With the variable delay task, triazolam but not pentobarbital interacted with the delay interval and produced impairments only at the 16-second delay condition. These data indicate that both triazolam and pentobarbital quantitatively impair acquisitional processes involved in short-term recall performance. Furthermore, triazolam may have a greater potential than pentobarbital to produce memory impairment, as reflected by its greater relative potency on these measures and its tendency to interfere with retention over short delay intervals.
采用双盲、拉丁方、平衡交叉设计,在7名正常男性志愿者中研究了安慰剂、三唑仑(0.25、0.5和0.75毫克)和戊巴比妥(100、200和300毫克)的效果。在上午10点左右口服药物之前及之后,每隔一小时,受试者完成对药物效果、精神运动表现任务的主观评分,以及数字回忆任务的两个版本,其中通过在数字键盘上再现来回忆八位数的刺激。在一个版本中,数字刺激在视频屏幕上显示不同的时长(3、6或9秒)后立即回忆。在另一个版本中,受试者首先再现持续显示的数字,然后在立即或16秒延迟间隔后回忆该数字。三唑仑和戊巴比妥对所有测量指标均产生剂量相关效应。相对效价比较表明,在主观评分和精神运动测量方面,三唑仑的效力比戊巴比妥高270 - 384倍,但在回忆损害测量方面,三唑仑的效力比戊巴比妥高406 - 647倍。在短(3秒)刺激呈现时间下,三唑仑和戊巴比妥产生的回忆表现缺陷在较长呈现时间下会减弱。在可变延迟任务中,三唑仑而非戊巴比妥与延迟间隔相互作用,仅在16秒延迟条件下产生损害。这些数据表明,三唑仑和戊巴比妥在数量上都会损害短期回忆表现中涉及的获取过程。此外,三唑仑可能比戊巴比妥有更大的产生记忆损害的潜力,这体现在其在这些测量指标上更高的相对效力以及在短延迟间隔内干扰记忆保持的倾向。