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Haloperidol Impairs Learning and Error-related Negativity in Humans

机译:氟哌啶醇损害人类的学习和与错误相关的负性

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摘要

Humans are able to monitor their actions for behavioral conflicts and performance errors. Growing evidence suggests that the error-related negativity (ERN) of the event-related cortical brain potential (ERP) may index the functioning of this response monitoring system and that the ERN may depend on dopaminergic mechanisms. We examined the role of dopamine in ERN and behavioral indices of learning by administering either 3 mg of the dopamine antagonist (DA) haloperidol (n = 17); 25 mg of diphenhydramine (n = 16), which has a similar CNS profile but without DA properties; or placebo (n = 18) in a randomized, double-blind manner to healthy volunteers. Three hours after drug administration, participants performed a goo-go Continuous Performance Task, the Eriksen Flanker Task, and a learning-dependent Time Estimation Task. Haloperidol significantly attenuated ERN amplitudes recorded during the flanker task, impaired learning of time intervals, and tended to cause more errors of commission, compared to placebo, which did not significantly differ from diphenhydramine. Drugs had no significant effects on the stimulus-locked P1 and N2 ERPs or on behavioral response latencies, but tended to affect post-error reaction time (RT) latencies in opposite ways (haloperidol decreased and diphenhydramine increased RTs). These findings support the hypothesis that the DA system is involved in learning and the generation of the ERN.
机译:人类能够监控自己的行为,以发现行为冲突和性能错误。越来越多的证据表明,与事件相关的皮质脑电势(ERP)的与错误相关的负电性(ERN)可能会指示该反应监测系统的功能,并且ERN可能取决于多巴胺能机制。我们通过服用3 mg多巴胺拮抗剂(DA)氟哌啶醇(n = 17)来检查多巴胺在ERN和学习行为指数中的作用; 25 mg苯海拉明(n = 16),具有相似的中枢神经系统特征,但无DA特性;或安慰剂(n = 18),以随机,双盲方式向健康志愿者提供。服药三小时后,参与者执行了继续执行的连续表现任务,Eriksen Flanker任务和依赖于学习的时间估计任务。与安慰剂相比,氟哌啶醇显着降低了在侧翼任务期间记录的ERN振幅,削弱了时间间隔的学习,并倾向于引起更多的委托错误,与苯海拉明没有显着差异。药物对刺激锁定的P1和N​​2 ERPs或行为反应潜伏期均无显着影响,但倾向于以相反的方式影响错误后反应时间(RT)潜伏期(氟哌啶醇减少,苯海拉明增加,RTs)。这些发现支持了DA系统参与学习和ERN生成的假设。

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