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Expressions of Neuregulin 1β and ErbB4 in Prefrontal Cortex and Hippocampus of a Rat Schizophrenia Model Induced by Chronic MK-801 Administration

机译:慢性MK-801诱导的大鼠精神分裂症模型前额叶皮质和海马神经调节蛋白1β和ErbB4的表达。

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摘要

Recent human genetic studies and postmortem brain examinations of schizophrenia patients strongly indicate that dysregulation of NRG1 and ErbB4 may be important pathogenic factors of schizophrenia. However, this hypothesis has not been validated and fully investigated in animal models of schizophrenia. In this study we quantitatively examined NRG1 and ErbB4 protein expressions by immunohistochemistry and Western blot in the brain of a rat schizophrenia model induced by chronic administration of MK-801 (a noncompetitive NMDA receptor antagonist). Our data showed that NRG1β and ErbB4 expressions were significantly increased in the rat prefrontal cortex and hippocampus but in different subregions. These findings suggest that altered expressions of NRG1 and ErbB4 might be attributed to the schizophrenia. Further study in the role and mechanism of NRG1 and ErbB4 may lead to better understanding of the pathophysiology for this disorder.
机译:最近的人类遗传学研究和精神分裂症患者的事后脑部检查强烈表明NRG1和ErbB4的失调可能是精神分裂症的重要致病因素。但是,该假设尚未在精神分裂症的动物模型中得到验证和充分研究。在这项研究中,我们通过免疫组织化学和蛋白质印迹法定量检测了慢性给药MK-801(一种非竞争性NMDA受体拮抗剂)诱导的大鼠精神分裂症模型的大脑中NRG1和ErbB4蛋白的表达。我们的数据表明,在大鼠前额叶皮层和海马中,NRG1β和ErbB4的表达明显增加,但在不同的子区域中。这些发现表明,NRG1和ErbB4表达的改变可能归因于精神分裂症。进一步研究NRG1和ErbB4的作用和机制可能会导致对该疾病的病理生理学有更好的了解。

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