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慢性苯丙胺或氟哌啶醇诱导的超敏反应破坏大鼠的潜伏抑制:与精神分裂症注意力障碍的关系。

Disrupted latent inhibition in the rat with chronic amphetamine or haloperidol-induced supersensitivity: relationship to schizophrenic attention disorder.

作者信息

Solomon P R, Crider A, Winkelman J W, Turi A, Kamer R M, Kaplan L J

出版信息

Biol Psychiatry. 1981 Jun;16(6):519-37.

PMID:7196265
Abstract

Latent inhibition (LI) is an attentional process by which animals learn to ignore a stimulus that is repeatedly presented without reinforcement. This ability to tune out a motivationally irrelevant stimulus is disrupted by pharmacological manipulations producing hyperdopaminergic states. In Experiment I, LI was disrupted following five daily administrations of 4 mg/kg d-amphetamine. In Experiment II the disruptive effects of d-amphetamine were eliminated by concomitant administration of chlorpromazine. Experiment III showed that LI could also be disrupted with 1 mg/kg d-amphetamine coupled with dopamine receptor supersensitivity produced by prolonged pretreatment with haloperidol. These data suggest that pharmacological disruption of LI may provide an animal analogue of the defective stimulus filtering thought to characterize at least some forms of schizophrenia.

摘要

潜伏抑制(LI)是一种注意力过程,通过该过程动物学会忽略在没有强化的情况下反复呈现的刺激。这种排除动机上无关刺激的能力会因产生高多巴胺能状态的药物操作而受到干扰。在实验I中,每天给予4毫克/千克的右旋苯丙胺,连续五天后,潜伏抑制受到干扰。在实验II中,通过同时给予氯丙嗪消除了右旋苯丙胺的干扰作用。实验III表明,1毫克/千克的右旋苯丙胺与通过长期用氟哌啶醇预处理产生的多巴胺受体超敏反应相结合,也会破坏潜伏抑制。这些数据表明,潜伏抑制的药理学破坏可能提供一种动物模型,模拟被认为是至少某些形式精神分裂症特征的有缺陷的刺激过滤。

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