首页> 外文期刊>Behavioural Brain Research: An International Journal >Effects of risperidone, clozapine and the 5-HT6 antagonist GSK-742457 on PCP-induced deficits in reversal learning in the two-lever operant task in male Sprague Dawley rats
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Effects of risperidone, clozapine and the 5-HT6 antagonist GSK-742457 on PCP-induced deficits in reversal learning in the two-lever operant task in male Sprague Dawley rats

机译:利培酮,氯氮平和5-HT6拮抗剂GSK-742457对雄性Sprague Dawley大鼠双杠杆操作中PCP诱导的逆向学习缺陷的影响

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Reasoning and problem solving deficits have been reported in schizophrenic patients. In the present study, we have tested rats in a two-lever reversal learning task in a Skinner box to model these deficits. In other studies using the Skinner box, atypical antipsychotics fully reversed phencyclidine (PCP)-induced impairments in reversal learning which is in contrast to clinical observations where antipsychotics lack the ability to fully reverse cognitive deficits in schizophrenia. Therefore, it can be argued that the outcome of these tests may lack predictive value.In the present study, after training on a spatial discrimination between two levers, rats were exposed to a reversal of the previously learned stimulus-response contingency during 5 days. We first investigated the effects of sub-chronic treatment with the non-competitive N-methyl-d-aspartate (NMDA) antagonists dizocilpine (MK-801) and PCP on reversal learning and extinction in male Sprague Dawley rats. Subsequently, we studied the effects of different PCP treatment regimes. Then, we investigated whether the atypical antipsychotics risperidone and clozapine and the 5-hydroxytryptamine6 (5-HT6) antagonist GSK-742457 could reverse the PCP-induced deficits. All drugs were administered subcutaneously (s.c.).MK-801 did not impair reversal learning, while PCP (1.0 and 2.0. mg/kg) induced a clear deficit in reversal learning. Both compounds, however, disrupted extinction at all tested doses. Risperidone and clozapine were both ineffective in significantly ameliorating the PCP-induced deficit in reversal learning which fits well with the clinical observations. The lowest dose of clozapine (1.25. mg/kg) had an intermediate effect in ameliorating the deficit in reversal learning induced by PCP (not different from control or PCP-treated rats). The lowest dose of GSK-742457 (0.63. mg/kg) fully reversed the PCP-induced deficits while the higher dose (5.0. mg/kg) had an intermediate effect. ? 2013 Elsevier B.V.
机译:据报道,精神分裂症患者的推理能力和解决问题的能力不足。在本研究中,我们在Skinner盒中的两个杠杆逆向学习任务中对大鼠进行了测试,以模拟这些缺陷。在其他使用Skinner盒的研究中,非典型抗精神病药完全逆转了苯环利定(PCP)所致的逆向学习障碍,这与临床观察相反,其中抗精神病药缺乏完全逆转精神分裂症认知缺陷的能力。因此,可以说这些测试的结果可能缺乏预测价值。在本研究中,在对两个杠杆之间的空间区分进行训练后,大鼠在5天内经历了先前学习的刺激反应偶然性的逆转。我们首先研究了非竞争性N-甲基-d-天冬氨酸(NMDA)拮抗剂地佐西平(MK-801)和PCP对亚慢性治疗对雄性Sprague Dawley大鼠逆向学习和消退的影响。随后,我们研究了不同PCP治疗方案的效果。然后,我们调查了非典型抗精神病药利培酮和氯氮平以及5-羟色胺6(5-HT6)拮抗剂GSK-742457是否可以逆转PCP诱导的缺陷。所有药物均皮下给药(s.c。)。MK-801不会损害逆向学习,而PCP(1.0和2.0.mg/kg)导致逆向学习明显不足。然而,这两种化合物在所有测试剂量下都破坏了灭绝。利培酮和氯氮平均不能有效改善PCP所致的逆向学习障碍,这与临床观察非常吻合。最低剂量的氯氮平(1.25。mg / kg)在缓解PCP诱导的逆向学习缺陷方面具有中间作用(与对照组或PCP处理的大鼠没有区别)。最低剂量的GSK-742457(0.63。mg / kg)完全逆转了PCP引起的缺陷,而较高的剂量(5.0。mg / kg)具有中等作用。 ? 2013 Elsevier B.V.

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