Newhouse P A, Potter A, Corwin J, Lenox R
Department of Psychiatry, University of Vermont College of Medicine, Burlington 05401.
Psychopharmacology (Berl). 1992;108(4):480-4. doi: 10.1007/BF02247425.
Single oral doses of the central and peripheral nicotinic antagonist mecamylamine were administered to healthy young normal males in doses of 5, 10, and 20 mg in a placebo-controlled, double-blind study. The 20 mg dose caused a significant increase in errors in the learning condition of the Repeated Acquisition task, producing a slower acquisition curve. The lower doses produced less errors, but more than in the placebo condition. There was no effect of drug on the performance component (retrieval of previously learned information). On the recognition memory task, dose-related increases in false-alarms during the delay period were seen, with little effect on misses or hits. Reaction time measures suggested a dose-related slowing of RT on several tasks. Behavioral effects were minimal and physiologic measures were consistent with dose-related ganglionic blockade. We interpret these results to indicate that acute blockade of nicotinic receptor function can produce measurable and significant cognitive impairment, even in non-smoking normals.
在一项安慰剂对照的双盲研究中,对健康年轻正常男性单次口服中枢和外周烟碱拮抗剂美加明,剂量分别为5毫克、10毫克和20毫克。20毫克剂量导致重复习得任务学习条件下的错误显著增加,产生了更慢的习得曲线。较低剂量产生的错误较少,但比安慰剂组多。药物对表现成分(检索先前学习的信息)没有影响。在识别记忆任务中,在延迟期内与剂量相关的错误警报增加,对漏报或命中的影响很小。反应时间测量表明,在几项任务中与剂量相关的反应时间减慢。行为影响最小,生理测量结果与剂量相关的神经节阻滞一致。我们将这些结果解释为表明,即使在不吸烟的正常人中,烟碱受体功能的急性阻断也会产生可测量的显著认知障碍。