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“经典”与“非经典”抗精神病药物:对苯丙胺和阿扑吗啡诱导的新纹状体及伏隔核自发神经元活动改变的差异拮抗作用

"Classical" and "atypical" antipsychotic drugs: differential antagonism of amphetamine- and apomorphine-induced alterations of spontaneous neuronal activity in the neostriatum and nucleus accumbens.

作者信息

Rebec G V, Bashore T R, Zimmerman K S, Alloway K D

出版信息

Pharmacol Biochem Behav. 1979 Nov;11(5):529-38. doi: 10.1016/0091-3057(79)90036-4.

Abstract

The ability of clozapine and haloperidol to antagonize the depression of firing rate produced by d-amphetamine and apomorphine in the neostriatum and nucleus accumbens was tested in immobilized, locally anesthetized rats. In the neostriatum, an intraperitoneal injection of 2.5 mg/kg d-amphetamine or 1.0 mg/kg apomorphine produced a prolonged inhibition of neuronal activity that was reversed by a subjsequent injection of either 20 mg/kg clozapine or 2.0 mg/kg haloperidol. An analysis of the onset and magnitude of the blockade revealed that clozapine was more effective than haloperidol in reversing the amphetamine response but that both antipsychotic drugs produced a comparable blockade of the apomorphine-induced depression. Similar results were obtained in the nucleus accumbens. The data indicate that although clozapine acts equieffectively in the neostriatum and nucleus accumbens, this atypical antipsychotic drug, aside from blocking postsynaptic dopamine receptors, may exert at least some of its effects by preventing dopamine release.

摘要

在固定、局部麻醉的大鼠中测试了氯氮平和氟哌啶醇拮抗由d-苯丙胺和阿扑吗啡引起的新纹状体和伏隔核放电率降低的能力。在新纹状体中,腹腔注射2.5mg/kg d-苯丙胺或1.0mg/kg阿扑吗啡会产生神经元活动的长期抑制,随后注射20mg/kg氯氮平或2.0mg/kg氟哌啶醇可逆转这种抑制。对阻断的起效和程度进行分析表明,氯氮平在逆转苯丙胺反应方面比氟哌啶醇更有效,但两种抗精神病药物对阿扑吗啡诱导的抑制产生的阻断作用相当。在伏隔核中也获得了类似的结果。数据表明,尽管氯氮平在新纹状体和伏隔核中的作用效果相同,但这种非典型抗精神病药物除了阻断突触后多巴胺受体外,可能至少部分通过阻止多巴胺释放发挥其作用。

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