首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The early changes in behavior and the myelinated fibers of the white matter in the Tg2576 transgenic mouse model of Alzheimer's disease
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The early changes in behavior and the myelinated fibers of the white matter in the Tg2576 transgenic mouse model of Alzheimer's disease

机译:Tg2576转基因阿尔茨海默氏病小鼠模型中行为的早期变化和白质的髓鞘纤维

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摘要

Recently, increasing evidences have indicated that abnormal behavior and white matter changes had appeared before senile plaques were formed in Alzheimer's disease (AD). However, the exact nature of these changes in behavior and white matter structure in early AD are unclear. This study used the Morris water maze, an ELISA assay, a transmission electron microscopic technique and new stereological methods to investigate the behavior, Aβ protein expression and white matter structure of Tg2576 transgenic mice at four ages. Only 10 months of age, the time latency in the Morris water maze tasks for Tg2576 transgenic mice were significantly longer than that of wild-type mice. The concentration of Aβ40 protein in the white matter of the Tg2576 transgenic mice was significantly increased in four ages mice, but the Aβ42 protein was significantly increased only in the 6-month-old mice. In 10-month-old mice, the axon volume in the white matter of the Tg2576 transgenic mice was significantly decreased when compared to the wild-type mice. These results suggest that the deposition of Aβ in the white matter of Tg2576 transgenic mice appeared before the spatial memory decline. The early detection of the Aβ content in the white matter of AD might help diagnose suspected AD. In addition, the axon changes in the white matter of AD might be one of the morphological causes of the behavioral deficits observed in 10-month-old transgenic mouse models of AD, and protecting the axons in the white matter might be an important method for delaying the progression of AD.
机译:最近,越来越多的证据表明在阿尔茨海默氏病(AD)中形成老年斑之前,已经出现了异常行为和白质变化。然而,尚不清楚AD早期这些行为和白质结构改变的确切性质。这项研究使用莫里斯水迷宫,ELISA分析,透射电子显微镜技术和新的体视学方法研究了四个年龄的Tg2576转基因小鼠的行为,Aβ蛋白表达和白质结构。仅10个月大时,Tg2576转基因小鼠的Morris水迷宫任务中的时间潜伏期明显长于野生型小鼠。 Tg2576转基因小鼠白质中Aβ40蛋白的浓度在四个年龄小鼠中显着增加,但是Aβ42蛋白仅在6个月大的小鼠中显着增加。与野生型小鼠相比,在10个月大的小鼠中,Tg2576转基因小鼠的白质中轴突体积显着减少。这些结果表明,Tg2576转基因小鼠的白质中Aβ的沉积出现在空间记忆下降之前。及早发现AD白质中Aβ含量可能有助于诊断可疑AD。此外,AD白质的轴突变化可能是在10个月大的AD转基因小鼠模型中观察到的行为缺陷的形态学原因之一,保护白质中的轴突可能是一种重要的方法。延缓AD的发展。

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