Naderi Mobin, Ghazvini Hamed, Maleksabet Amir, Ghalehnoei Hossein, Khajavi Rezvan
Student Research Committee, Faculty of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
J Mol Neurosci. 2025 Aug 12;75(3):106. doi: 10.1007/s12031-025-02403-x.
Schizophrenia, a severe neuropsychiatric disorder, is characterized by significant impairments in neurological function. The disease includes a spectrum of symptoms that are divided into four main categories: positive, negative, cognitive, and mood symptoms. In this study, 32 male Wistar rats, approximately 10 to 12 weeks old, were randomly separated into four groups: vehicle (saline), ketamine (30 mg/kg), aripiprazole (0.75 mg/kg), and risperidone (1 mg/kg). Twenty-four hours following the final ketamine or saline administration, social interaction test (SIT), open field test (OFT), novel object recognition (NOR), and elevated plus-maze (EPM) were performed on the animals. Hippocampal tissue was used for molecular analysis using Real-Time PCR technique. Behavioral tests revealed that both risperidone and aripiprazole reduced anxiety-like behaviors and enhanced cognitive discrimination. At the molecular level, hippocampal expression of DRD2 and HTR2A did not differ significantly across groups. However, the ketamine-treated group exhibited elevated AKT1 expression relative to the vehicle group, whereas risperidone administration downregulated AKT1 compared to the ketamine group. Notably, CACNA1C expression was upregulated in the aripiprazole group compared to both the ketamine and vehicle groups. The findings of this study showed that the antipsychotic drugs risperidone and aripiprazole have the ability to moderately alleviate cognitive deficits in rats. The results also indicated that this treatment may affect the gene expression of AKT1, and CACNA1C genes.
精神分裂症是一种严重的神经精神障碍,其特征是神经功能存在显著损害。该疾病包括一系列症状,这些症状分为四个主要类别:阳性、阴性、认知和情绪症状。在本研究中,32只雄性Wistar大鼠,年龄约10至12周,被随机分为四组:溶剂对照组(生理盐水)、氯胺酮(30毫克/千克)、阿立哌唑(0.75毫克/千克)和利培酮(1毫克/千克)。在最后一次给予氯胺酮或生理盐水24小时后,对动物进行社会互动测试(SIT)、旷场试验(OFT)、新物体识别测试(NOR)和高架十字迷宫试验(EPM)。使用实时PCR技术对海马组织进行分子分析。行为测试表明,利培酮和阿立哌唑均可减少焦虑样行为并增强认知辨别能力。在分子水平上,各组间DRD2和HTR2A的海马表达无显著差异。然而,与溶剂对照组相比,氯胺酮处理组的AKT1表达升高,而与氯胺酮组相比,利培酮给药使AKT1表达下调。值得注意的是,与氯胺酮组和溶剂对照组相比,阿立哌唑组的CACNA1C表达上调。本研究结果表明,抗精神病药物利培酮和阿立哌唑有能力适度减轻大鼠的认知缺陷。结果还表明,这种治疗可能会影响AKT1和CACNA1C基因的表达。