Hashimoto Kenji, Fujita Yuko, Shimizu Eiji, Iyo Masaomi
Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, 1-8-1 Inohana, Chiba 260-8670, Japan.
Eur J Pharmacol. 2005 Sep 5;519(1-2):114-7. doi: 10.1016/j.ejphar.2005.07.002.
This study was undertaken to examine the effects of subsequent administration of antipsychotic drugs (clozapine and haloperidol) on cognitive deficits in mice after repeated administration of phencyclidine (PCP). In the novel object recognition test, repeated administration of PCP (10 mg/kg) significantly decreased exploratory preference in the retention test session but not in the training test session. PCP-induced deficits were significantly improved by subsequent subchronic (2 weeks) administration of clozapine (5 mg/kg), but not haloperidol (0.1 mg/kg). These findings suggest that PCP-induced cognitive deficits using the novel object recognition test may be a potential animal model of atypical antipsychotic activity.
本研究旨在探讨在小鼠反复给予苯环利定(PCP)后,后续给予抗精神病药物(氯氮平和氟哌啶醇)对认知缺陷的影响。在新颖物体识别测试中,反复给予PCP(10mg/kg)显著降低了在记忆测试阶段的探索偏好,但在训练测试阶段未出现此现象。PCP诱导的缺陷通过后续亚慢性(2周)给予氯氮平(5mg/kg)得到显著改善,但给予氟哌啶醇(0.1mg/kg)则无此效果。这些发现表明,使用新颖物体识别测试的PCP诱导认知缺陷可能是一种非典型抗精神病活性的潜在动物模型。