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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Cortical distribution of neurofibrillary tangles in Alzheimer's disease matches the pattern of neurons that retain their capacity of plastic remodelling in the adult brain.
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Cortical distribution of neurofibrillary tangles in Alzheimer's disease matches the pattern of neurons that retain their capacity of plastic remodelling in the adult brain.

机译:阿尔茨海默氏病中神经原纤维缠结的皮质分布与在成人大脑中保留其塑性重塑能力的神经元模式相匹配。

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The formation of neurofibrillary tangles in Alzheimer's disease shows a preferential involvement of certain cytoarchitecturally defined cortical areas suggesting systematic differences in regional neuronal vulnerability. The cellular and molecular nature of this selective neuronal vulnerability that follows a certain hierarchy of structural brain organization is largely unknown. In the present study, we compared the regional pattern of tangle density in Alzheimer's disease with systematic regional differences in neuronal plasticity that can be observed both during ageing and in Alzheimer's disease. Changes in dendritic length and arborization of Golgi-impregnated pyramidal neurons were analysed after three-dimensional reconstruction in 12 cortical areas. The intensity of dendritic remodelling that was observed during ageing as well as in Alzheimer's disease was regionally different and decreased in the following order: transentorhinal region > limbic areas (entorhinal region, hippocampus) > non-primary association areas (37, 40, 46) > primary sensory association areas (7, 18, 22) > primary sensory and motor cortex (17, 41, 4). These regional differences of neuronal plasticity follow the same pattern as the regional vulnerability to tangle formation in Alzheimer's disease. The results of the present study provide evidence that a high degree of structural neuronal plasticity might predispose neurons to tangle formation.
机译:阿尔茨海默氏病中神经原纤维缠结的形成表明某些细胞结构明确定义的皮质区域优先参与,提示区域神经元易损性存在系统性差异。选择性的神经元脆弱性遵循一定的大脑结构组织层次的细胞和分子性质在很大程度上是未知的。在本研究中,我们将阿尔茨海默氏病中缠结密度的区域模式与神经元可塑性的系统性区域差异进行了比较,这可以在衰老过程中和阿尔茨海默氏病中观察到。在12个皮质区域进行三维重建后,分析了高尔基浸渍的锥体神经元的树突长度变化和乔式化。在衰老过程中以及在阿尔茨海默氏病中观察到的树突重塑的强度在区域上有所不同,并以下列顺序降低:跨肠胃区>边缘区(肠内区,海马区)>非初级结缔组织区(37、40、46) >初级感觉关联区域(7、18、22)>初级感觉和运动皮层(17、41、4)。这些神经元可塑性的区域差异与阿尔茨海默氏病中缠结形成的区域脆弱性遵循相同的模式。本研究的结果提供了证据,表明高度的结构神经元可塑性可能使神经元易于缠结。

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