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非典型抗精神病药物瑞莫必利增强大鼠的潜伏抑制。

Enhancement of latent inhibition in the rat by the atypical antipsychotic agent remoxipride.

作者信息

Trimble K M, Bell R, King D J

机构信息

Department of Therapeutics and Pharmacology, Queen's University of Belfast, Northern Ireland.

出版信息

Pharmacol Biochem Behav. 1997 Apr;56(4):809-16. doi: 10.1016/s0091-3057(96)00483-2.

Abstract

Latent inhibition (LI) is a behavioural paradigm in which repeated nonreinforced preexposure to a stimulus inhibits the formation of subsequent associations to that stimulus. LI is believed to reflect learning to ignore irrelevant stimuli. Disrupted LI has been suggested as an animal model for the attentional deficits observed in schizophrenia. Remoxipride, a selective dopamine D, antagonist, is an effective antipsychotic with an atypical clinical profile. We investigated the effects of remoxipride (1.0, 5.0, and 10.0 mg/kg) and haloperidol (0.1 mg/kg) administration on LI in rats. A three-stage conditioned emotional response procedure was employed: a) preexposure: preexposed rats received 10 presentations of a flashing light stimulus without reinforcement, and nonpreexposed rats received no exposure: b) conditioning; the preexposed stimulus was paired with a foot shock over a number of trials: c) test: LI was expressed by the extent of suppression of water licking during flashing light presentation. Animals receiving 0.1 mg/kg of haloperidol or 1.0 or 5.0 mg/kg (but not 10.0 mg/kg) of remoxipride treated the preexposed stimulus as irrelevant after a low number of preexposed. These results illustrate that the LI model is equally sensitive to typical and atypical antipsychotics and reemphasises its utility as a test model for detecting the antipsychotic potential of novel drugs.

摘要

潜伏抑制(LI)是一种行为范式,其中对刺激的重复非强化预暴露会抑制随后与该刺激形成的关联。LI被认为反映了学会忽略无关刺激。LI破坏已被提议作为精神分裂症中观察到的注意力缺陷的动物模型。瑞莫必利是一种选择性多巴胺D拮抗剂,是一种具有非典型临床特征的有效抗精神病药物。我们研究了给予大鼠瑞莫必利(1.0、5.0和10.0mg/kg)和氟哌啶醇(0.1mg/kg)对LI的影响。采用三阶段条件性情绪反应程序:a)预暴露:预暴露组大鼠接受10次无强化的闪光刺激呈现,未预暴露组大鼠未接受暴露;b)条件化:在多次试验中将预暴露的刺激与足部电击配对;c)测试:通过闪光呈现期间舔水抑制的程度来表示LI。接受0.1mg/kg氟哌啶醇或1.0或5.0mg/kg(但不是10.0mg/kg)瑞莫必利的动物在少量预暴露后将预暴露的刺激视为无关刺激。这些结果表明,LI模型对典型和非典型抗精神病药物同样敏感,并再次强调了其作为检测新药抗精神病潜力的测试模型的效用。

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