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瘙痒病感染小鼠海马CA3区锥体神经元中神经肽Y信使核糖核酸的异常诱导

Aberrant induction of neuropeptide Y mRNA in hippocampal CA3 pyramidal neurones in scrapie-infected mice.

作者信息

Diez M, Koistinaho J, DeArmond S J, Camerino A P, Groth D, Caytano J C, Prusiner S B, Hökfelt T

机构信息

Department of Neuroscience, Karolinska Institute, Stockholm, Sweden.

出版信息

Neuroreport. 1996 Aug 12;7(12):1887-92. doi: 10.1097/00001756-199608120-00003.

Abstract

The neurochemical alterations preceding neurological dysfunction and neuronal death in prion diseases are not well characterized. Here we examined, using in situ hybridization histochemistry, the expression of neuropeptide Y (NPY), an inducible and abundant neuropeptide in mammalian brain with known neuroregulatory functions, and glial fibrillary acidic protein (GFAP), a marker for astroglial activation, in the hippocampus at different time points following intracerebral prion inoculation in male CD-1 mice. Between 110 and 140 days postinoculation NPY mRNA expression was specifically up-regulated in CA3 pyramidal neurones, whereas expression of NPY in hilar neurones remained unaltered. Up-regulation of GFAP mRNA was observed in the CA1 stratum radiatum at 60 days, and spread throughout the hippocampus, cortex and thalamus between 110 and 140 days, suggesting early accumulation of scrapie prion protein in these regions. The clinical symptoms were first manifested 120 days postinoculation. Aberrant induction of NPY mRNA in the hippocampal CA3 pyramidal neurones preceded the onset of neurological symptoms, and may be involved in the regulation of glutamate release at the Schaffer collateral-CA1 synapses in scrapie-infected mice.

摘要

朊病毒疾病中神经功能障碍和神经元死亡之前的神经化学变化尚未得到充分表征。在此,我们使用原位杂交组织化学方法,检测了雄性CD-1小鼠脑内接种朊病毒后不同时间点海马体中神经肽Y(NPY)的表达,NPY是哺乳动物脑中一种可诱导且丰富的神经肽,具有已知的神经调节功能,以及胶质纤维酸性蛋白(GFAP),一种星形胶质细胞活化的标志物。接种后110至140天之间,CA3锥体神经元中NPY mRNA表达特异性上调,而门区神经元中NPY的表达保持不变。在60天时,CA1辐射层中观察到GFAP mRNA上调,并在110至140天之间扩散至整个海马体、皮质和丘脑,提示瘙痒病朊病毒蛋白在这些区域早期积聚。临床症状在接种后120天首次出现。海马体CA3锥体神经元中NPY mRNA的异常诱导先于神经症状的发作,可能参与了瘙痒病感染小鼠中Schaffer侧支-CA1突触处谷氨酸释放的调节。

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