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阿尔茨海默病中神经原纤维缠结的皮质分布与成人大脑中保留可塑性重塑能力的神经元模式相匹配。

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.

作者信息

Arendt T, Brückner M K, Gertz H J, Marcova L

机构信息

Paul Flechsig Institute of Brain Research, Department of Neuroanatomy, Leipzig, Germany.

出版信息

Neuroscience. 1998 Apr;83(4):991-1002. doi: 10.1016/s0306-4522(97)00509-5.

Abstract

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.

摘要

阿尔茨海默病中神经原纤维缠结的形成显示出某些细胞结构定义的皮质区域优先受累,这表明区域神经元易损性存在系统性差异。这种遵循特定脑组织结构层次的选择性神经元易损性的细胞和分子本质在很大程度上尚不清楚。在本研究中,我们将阿尔茨海默病中缠结密度的区域模式与在衰老过程和阿尔茨海默病中均可观察到的神经元可塑性的系统性区域差异进行了比较。对12个皮质区域经三维重建后的高尔基染色锥体神经元的树突长度和分支变化进行了分析。在衰老过程以及阿尔茨海默病中观察到的树突重塑强度存在区域差异,且按以下顺序降低:嗅周区域>边缘区域(内嗅区域、海马体)>非初级联合区域(37、40、46)>初级感觉联合区域(7、18、22)>初级感觉和运动皮质(17、41、4)。神经元可塑性的这些区域差异与阿尔茨海默病中缠结形成的区域易损性遵循相同模式。本研究结果提供了证据,即高度的神经元结构可塑性可能使神经元易形成缠结。

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