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6-羟基多巴胺诱导的帕金森病大鼠模型中,小胶质细胞激活及含多巴胺神经元变性的动力学研究

Kinetics of microglial activation and degeneration of dopamine-containing neurons in a rat model of Parkinson disease induced by 6-hydroxydopamine.

作者信息

Henry Vincent, Paillé Vincent, Lelan Faustine, Brachet Philippe, Damier Philippe

机构信息

Institut National de la Santé et de la Recherche Médicale, UMR 643,CHU de Nantes, Nantes Cedex 01, France.

出版信息

J Neuropathol Exp Neurol. 2009 Oct;68(10):1092-102. doi: 10.1097/NEN.0b013e3181b767b4.

Abstract

In both Parkinson disease and in animal models of Parkinson disease, there is a microglial reaction in addition to the loss of dopaminergic neurons in the ventral midbrain. To determine the pathological role of this microglial reaction, we analyzed the kinetics of microglial activation and dopaminergic cell death induced in rats with the neurotoxin 6-hydroxydopamine. As early as Day 1 after the injection, there was a decline in the motor performance of the 6-hydroxydopamine-lesioned rats that correlated with a reduction of dopaminergic innervation of the contralateral striatum. Loss of dopaminergic neurons in the ventral midbrain developed a few days later and seemed to follow a specific temporospatial pattern. Degenerating neurons and activated microglia were seen only in areas in which dopaminergic cells were no longer observed, suggesting that the loss of the dopaminergic phenotype preceded the degenerative process. In sham-lesioned rats, there was a transient activation of microglia in the vicinity of the needle tract without any cell degeneration. This chronology of events supports the hypothesis that microglial activation is a secondary rather than primary phenomenon in dopaminergic cell degeneration induced by 6-hydroxydopamine.

摘要

在帕金森病以及帕金森病动物模型中,除了中脑腹侧多巴胺能神经元丧失外,还存在小胶质细胞反应。为了确定这种小胶质细胞反应的病理作用,我们分析了用神经毒素6-羟基多巴胺诱导的大鼠小胶质细胞激活和多巴胺能细胞死亡的动力学。早在注射后第1天,6-羟基多巴胺损伤大鼠的运动能力就出现下降,这与对侧纹状体多巴胺能神经支配减少相关。中脑腹侧多巴胺能神经元的丧失在几天后出现,且似乎遵循特定的时空模式。仅在不再观察到多巴胺能细胞的区域可见退化的神经元和活化的小胶质细胞,这表明多巴胺能表型的丧失先于退化过程。在假损伤大鼠中,针道附近的小胶质细胞有短暂激活,但无任何细胞退化。这些事件的时间顺序支持这样的假说,即在6-羟基多巴胺诱导的多巴胺能细胞退化中,小胶质细胞激活是一种继发而非原发现象。

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