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Age and Environment Influences on Mouse Prion Disease Progression: Behavioral Changes and Morphometry and Stereology of Hippocampal Astrocytes

机译:年龄和环境对小鼠Pri病毒疾病进展的影响:海马星形胶质细胞的行为变化以及形态学和体视学

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摘要

Because enriched environment (EE) and exercise increase and aging decreases immune response, we hypothesized that environmental enrichment and aging will, respectively, delay and increase prion disease progression. Mice dorsal striatum received bilateral stereotaxic intracerebral injections of normal or ME7 prion infected mouse brain homogenates. After behavior analysis, animals were euthanized and their brains processed for astrocyte GFAP immunolabeling. Our analysis related to the environmental influence are limited to young adult mice, whereas age influence refers to aged mice raised on standard cages. Burrowing activity began to reduce in ME7-SE two weeks before ME7-EE, while no changes were apparent in ME7 aged mice (ME7-A). Object placement recognition was impaired in ME7-SE, NBH-A, and ME7-A but normal in all other groups. Object identity recognition was impaired in ME7-A. Cluster analysis revealed two morphological families of astrocytes in NBH-SE animals, three in NBH-A and ME7-A, and four in NBH-EE, ME7-SE, and ME7-EE. As compared with control groups, astrocytes from DG and CA3 prion-diseased animals show significant numerical and morphological differences and environmental enrichment did not reverse these changes but induced different morphological changes in GFAP+ hippocampal astroglia. We suggest that environmental enrichment and aging delayed hippocampal-dependent behavioral and neuropathological signs of disease progression.
机译:由于丰富的环境(EE)和运动增加以及衰老会降低免疫反应,因此我们假设环境的丰富化和衰老会分别延迟和增加increase病毒疾病的进展。小鼠背侧纹状体接受正常或ME7 ion病毒感染的小鼠脑匀浆的双侧立体定向脑内注射。行为分析后,对动物实施安乐死并对其大脑进行星形胶质细胞GFAP免疫标记处理。我们与环境影响有关的分析仅限于成年小鼠,而年龄影响则是指在标准笼中饲养的老年小鼠。在ME7-EE出现前两周,ME7-SE中的挖穴活动开始减少,而在ME7衰老小鼠(ME7-A)中则没有明显变化。对象放置识别在ME7-SE,NBH-A和ME7-A中受损,但在所有其他组中均正常。 ME7-A中的对象身份识别受到损害。聚类分析显示,NBH-SE动物中有两个星形胶质细胞形态家族,NBH-A和ME7-A中三个,NBH-EE,ME7-SE和ME7-EE中四个。与对照组相比,来自DG和CA3 ion病毒病动物的星形胶质细胞显示出明显的数字和形态差异,环境富集并不能逆转这些变化,但会诱发GFAP +海马星形胶质细胞的形态变化。我们建议环境丰富和衰老延迟了疾病进展的海马依赖性行为和神经病理学迹象。

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