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首页> 外文期刊>Journal of neuroinflammation >Microglial activation in the hippocampus of hypercholesterolemic rabbits occurs independent of increased amyloid production
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Microglial activation in the hippocampus of hypercholesterolemic rabbits occurs independent of increased amyloid production

机译:高胆固醇血症兔海马中的小胶质细胞激活发生,而与淀粉样蛋白产生增加无关

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Background Rabbits maintained on high-cholesterol diets are known to show increased immunoreactivity for amyloid beta protein in cortex and hippocampus, an effect that is amplified by presence of copper in the drinking water. Hypercholesterolemic rabbits also develop sporadic neuroinflammatory changes. The purpose of this study was to survey microglial activation in rabbits fed cholesterol in the presence or absence of copper or other metal ions, such as zinc and aluminum. Methods Vibratome sections of the rabbit hippocampus and overlying cerebral cortex were examined for microglial activation using histochemistry with isolectin B4 from Griffonia simplicifolia. Animals were scored as showing either focal or diffuse microglial activation with or without presence of rod cells. Results Approximately one quarter of all rabbits fed high-cholesterol diets showed evidence of microglial activation, which was always present in the hippocampus and not in the cortex. Microglial activation was not correlated spatially with increased amyloid immunoreactivity or with neurodegenerative changes and was most pronounced in hypercholesterolemic animals whose drinking water had been supplemented with either copper or zinc. Controls maintained on normal chow were largely devoid of neuroinflammatory changes, but revealed minimal microglial activation in one case. Conclusion Because the increase in intraneuronal amyloid immunoreactivity that results from administration of cholesterol occurs in both cerebral cortex and hippocampus, we deduce that the microglial activation reported here, which is limited to the hippocampus, occurs independent of amyloid accumulation. Furthermore, since neuroinflammation occurred in the absence of detectable neurodegenerative changes, and was also not accompanied by increased astrogliosis, we conclude that microglial activation occurs because of metabolic or biochemical derangements that are influenced by dietary factors.
机译:背景技术已知以高胆固醇饮食喂养的兔子在皮质和海马中对淀粉样β蛋白的免疫反应性增强,饮用水中铜的存在会放大这种效应。高胆固醇血症的兔子也会出现偶发的神经炎症改变。这项研究的目的是调查在有或没有铜或其他金属离子(如锌和铝)存在的情况下,饲喂胆固醇的兔子的小胶质细胞活化。方法采用单纯花葛异叶凝集素B4的组织化学方法,检测家兔海马及上覆大脑皮层的Vibratome小胶质细胞的活化。将动物评分为显示有或没有杆状细胞存在的局灶性或弥散性小胶质细胞活化。结果喂高胆固醇饮食的所有兔子中约有四分之一显示出小胶质细胞活化的迹象,该现象始终存在于海马而不是皮层中。小胶质细胞活化在空间上与淀粉样蛋白免疫反应性增加或神经退行性变化无关,在高胆固醇血症动物的饮用水中补充了铜或锌的情况下,小胶质细胞的激活最为明显。维持正常饮食的对照组在很大程度上没有神经炎症的改变,但是在一个病例中显示出最小的神经胶质细胞激活。结论由于施用胆固醇引起的神经内淀粉样蛋白免疫反应性增加发生在大脑皮层和海马体中,我们推断此处报道的仅限于海马体的小胶质细胞激活独立于淀粉样蛋白的积累而发生。此外,由于神经发炎是在没有可检测到的神经退行性变化的情况下发生的,并且也没有伴有星形胶质细胞增多症,因此我们得出结论,小胶质细胞活化的发生是由于受饮食因素影响的代谢或生化异常。

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