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氯氮平增加成年雄性大鼠海马巢蛋白浓度:一项初步研究。

Clozapine Increases Nestin Concentration in the Adult Male Rat Hippocampus: A Preliminary Study.

机构信息

Department of Biomedical Sciences, Ontario Veterinary College, University of Guelph, Guelph, ON N1G 2W1, Canada.

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada.

出版信息

Int J Mol Sci. 2022 Mar 22;23(7):3436. doi: 10.3390/ijms23073436.

Abstract

Patients with schizophrenia, and rodent models of the disease, both exhibit suppressed neurogenesis, with antipsychotics possibly enhancing neurogenesis in pre-clinical models. Nestin, a cytoskeletal protein, is implicated in neuronal differentiation and adult neurogenesis. We hypothesized that schizophrenia pathogenesis involves nestin downregulation; however, few studies have related nestin to schizophrenia. We assessed nestin protein concentration, prepulse inhibition (PPI), and social interaction in the MK-801 model of schizophrenia, with or without antipsychotic (clozapine) treatment. Adult male Sprague-Dawley rats were intraperitoneally administered saline or MK-801 (0.1 mg/kg) to produce a schizophrenia-like phenotype, with concomitant subcutaneous injections of vehicle or clozapine (5 mg/kg). PPI was assessed on days 1, 8, and 15, and social interaction was assessed on day 4. Hippocampus tissue samples were dissected for Western blotting of nestin concentration. MK-801 alone did not alter nestin concentration, while clozapine alone enhanced hippocampal nestin concentration; this effect was not apparent in animals with MK-801 and clozapine co-administration. MK-801 also produced schizophrenia-like PPI disruptions, some of which were reversed by clozapine. Social interaction deficits were not detected in this model. This is the first report of clozapine-induced enhancements of hippocampal nestin concentration that might be mediated by NMDA receptors. Future studies will explore the impact of neurodevelopmental nestin concentration on symptom onset and antipsychotic treatment.

摘要

精神分裂症患者和疾病的啮齿动物模型均表现出神经发生受抑制,而抗精神病药物可能会增强临床前模型中的神经发生。巢蛋白是一种细胞骨架蛋白,与神经元分化和成年神经发生有关。我们假设精神分裂症的发病机制涉及巢蛋白下调;然而,很少有研究将巢蛋白与精神分裂症联系起来。我们评估了 MK-801 精神分裂症模型中巢蛋白蛋白浓度、预脉冲抑制(PPI)和社会互动,以及有无抗精神病药物(氯氮平)治疗。成年雄性 Sprague-Dawley 大鼠腹腔内给予生理盐水或 MK-801(0.1mg/kg)以产生类似精神分裂症的表型,同时皮下注射载体或氯氮平(5mg/kg)。在第 1、8 和 15 天评估 PPI,在第 4 天评估社会互动。分离海马组织样本,用于巢蛋白浓度的 Western 印迹分析。MK-801 单独使用不会改变巢蛋白浓度,而氯氮平单独使用会增强海马巢蛋白浓度;在 MK-801 和氯氮平共同给药的动物中,这种作用并不明显。MK-801 还导致类似精神分裂症的 PPI 中断,其中一些中断可被氯氮平逆转。在这种模型中未检测到社会互动缺陷。这是首次报道氯氮平诱导的海马巢蛋白浓度增加,可能由 NMDA 受体介导。未来的研究将探讨神经发育巢蛋白浓度对症状发作和抗精神病药物治疗的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c31/8998718/1c4aba2f27af/ijms-23-03436-g001.jpg

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