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Regulation of Myelin Genes Implicated in Psychiatric Disorders by Functional Activity in Axons

机译:通过轴突的功能活动对精神疾病中涉及的髓磷脂基因的调节。

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摘要

Myelination is a highly dynamic process that continues well into adulthood in humans. Several recent gene expression studies have found abnormal expression of genes involved in myelination in the prefrontal cortex of brains from patients with schizophrenia and other psychiatric illnesses. Defects in myelination could contribute to the pathophysiology of psychiatric illness by impairing information processing as a consequence of altered impulse conduction velocity and synchrony between cortical regions carrying out higher level cognitive functions. Myelination can be altered by impulse activity in axons and by environmental experience. Psychiatric illness is treated by psychotherapy, behavioral modification, and drugs affecting neurotransmission, raising the possibility that myelinating glia may not only contribute to such disorders, but that activity-dependent effects on myelinating glia could provide one of the cellular mechanisms contributing to the therapeutic effects of these treatments. This review examines evidence showing that genes and gene networks important for myelination can be regulated by functional activity in axons.
机译:髓鞘形成是一个高度动态的过程,一直持续到人类成年。最近的几项基因表达研究发现,精神分裂症和其他精神疾病患者的大脑前额叶皮层中涉及髓鞘形成的基因表达异常。由于冲动传导速度的改变和执行更高水平的认知功能的皮层区域之间的同步性降低,信息处理受到损害,髓鞘化的缺陷可能有助于精神疾病的病理生理。髓鞘的冲动和环境经验可以改变髓鞘形成。精神疾病通过心理治疗,行为改变和影响神经传递的药物进行治疗,这增加了髓鞘神经胶质不仅可能导致此类疾病的可能性,而且对髓鞘神经胶质的活动依赖性作用可能提供了有助于治疗作用的细胞机制之一这些治疗方法。这项审查审查证据表明,对髓鞘形成重要的基因和基因网络可以通过轴突的功能活性来调节。

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