Jentsch J D, Redmond D E, Elsworth J D, Taylor J R, Youngren K D, Roth R H
Section of Neurobiology, Yale University School of Medicine, New Haven, CT, USA.
Science. 1997 Aug 15;277(5328):953-5. doi: 10.1126/science.277.5328.953.
The effects of the psychotomimetic drug phencyclidine on the neurochemistry and function of the prefrontal cortex in vervet monkeys were investigated. Monkeys treated with phencyclidine twice a day for 14 days displayed performance deficits on a task that was sensitive to prefrontal cortex function; the deficits were ameliorated by the atypical antipsychotic drug clozapine. Repeated exposure to phencyclidine caused a reduction in both basal and evoked dopamine utilization in the dorsolateral prefrontal cortex, a brain region that has long been associated with cognitive function. Behavioral deficits and decreased dopamine utilization remained after phencyclidine treatment was stopped, an indication that these effects were not simply due to direct drug effects. The data suggest that repeated administration of phencyclidine in monkeys may be useful for studying psychiatric disorders associated with cognitive dysfunction and dopamine hypofunction in the prefrontal cortex, particularly schizophrenia.
研究了拟精神病药物苯环利定对黑长尾猴前额叶皮质神经化学和功能的影响。每天用苯环利定治疗两次,持续14天的猴子在一项对前额叶皮质功能敏感的任务上表现出行为缺陷;非典型抗精神病药物氯氮平改善了这些缺陷。反复接触苯环利定导致背外侧前额叶皮质(一个长期以来与认知功能相关的脑区)的基础和诱发多巴胺利用减少。停止苯环利定治疗后,行为缺陷和多巴胺利用减少仍然存在,这表明这些影响不仅仅是由于药物的直接作用。数据表明,在猴子中反复给予苯环利定可能有助于研究与前额叶皮质认知功能障碍和多巴胺功能减退相关的精神疾病,尤其是精神分裂症。