结合LPS神经炎症模型突触囊泡相关蛋白和轴突转运蛋白动态变化的研究。

ISRN Neurology Pub Date : 2013-09-24 eCollection Date: 2013-01-01 DOI:10.1155/2013/496079
Rui Zhang, Ming Zhao, Hai-Jie Ji, Yu-He Yuan, Nai-Hong Chen
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引用次数: 6

摘要

小胶质细胞活化是构成神经退行性疾病特征的炎症的主要组成部分。大量研究表明,参与PD发病过程的炎症通过多种炎症因子的释放,激活作用于神经元的小胶质细胞。然而,其作用于神经元的分子机制尚不清楚。本研究表明,脑内注射LPS可诱导C57BL/6J小鼠帕金森病病理。进一步研究突触囊泡相关蛋白和轴突转运蛋白在此过程中的动态变化。结果表明,LPS给药后,大鼠脑内TNF- α和IL-1 β的炎症水平均升高,且具有时间依赖性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Study on the dynamic changes in synaptic vesicle-associated protein and axonal transport protein combined with LPS neuroinflammation model.

Study on the dynamic changes in synaptic vesicle-associated protein and axonal transport protein combined with LPS neuroinflammation model.

Study on the dynamic changes in synaptic vesicle-associated protein and axonal transport protein combined with LPS neuroinflammation model.

Study on the dynamic changes in synaptic vesicle-associated protein and axonal transport protein combined with LPS neuroinflammation model.

Microglia activation is the major component of inflammation that constitutes the characteristic of neurodegenerative disease. A large amount of researches have demonstrated that inflammation involved in the pathogenesis of PD process activated microglia acting on the neurons through the release of a variety of inflammatory factors. However, the molecular mechanism underlying how it does work on neurons is still unclear. Here, we show that intracerebral injections of LPS induced Parkinson's disease pathology in C57BL/6J mice. Furthermore, study on the dynamic changes in Synaptic vesicle-associated protein and axonal transport Protein in this process. The results indicated that after administration of LPS in the brain, the inflammatory levels of TNF- α and IL-1 β both are elevated, and have a time-dependent.

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