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猴免疫缺陷病毒脑病的神经元基质

Neuronal substrates for SIV encephalopathy.

作者信息

da Cunha A, Eiden L E, Rausch D M

机构信息

Section on Molecular Neuroscience, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.

出版信息

Adv Neuroimmunol. 1994;4(3):265-71. doi: 10.1016/s0960-5428(06)80266-4.

Abstract

Prior to the onset of immunodeficiency disease, neurochemical and neuropathological events associated with motor and/or cognitive impairment can be identified in rhesus monkeys infected with simian immunodeficiency virus (SIV). These are astrocytosis, up-regulation of mRNA encoding the neuropeptide somatostatin (SRIF) and an increased expression of MHC Class II antigen. End-stage immunodeficiency disease has been associated with robust viral expression in the CNS frequently observed as multinucleated giant cell formation. SIV encephalitis has not been observed in animals whose only clinical signs of SIV disease were motor and/or cognitive impairment. These data suggest that neuronal dysfunction discernable as altered neuropeptide expression in cortical neurons precedes frank structural damage to the CNS in SIV encephalopathy. This model is consistent with the mechanism of neuropathogenesis in human HIV encephalopathy that can be partially inferred from neurochemical and neuropathological examination of autopsy material in HIV disease.

摘要

在免疫缺陷疾病发作之前,感染猿猴免疫缺陷病毒(SIV)的恒河猴中可识别出与运动和/或认知障碍相关的神经化学和神经病理学事件。这些事件包括星形细胞增生、编码神经肽生长抑素(SRIF)的mRNA上调以及MHC II类抗原表达增加。终末期免疫缺陷疾病与中枢神经系统中强烈的病毒表达有关,这经常表现为多核巨细胞形成。在仅表现出SIV疾病的运动和/或认知障碍等临床症状的动物中未观察到SIV脑炎。这些数据表明,在SIV脑病中,可辨别为皮质神经元中神经肽表达改变的神经元功能障碍先于中枢神经系统出现明显的结构损伤。该模型与人类HIV脑病的神经发病机制一致,这可以从HIV疾病尸检材料的神经化学和神经病理学检查中部分推断出来。

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