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阿尔茨海默病脑中海马神经元脂褐素和神经原纤维缠结的定量分析。

Quantitative analysis of lipofuscin and neurofibrillary tangles in the hippocampal neurons of Alzheimer disease brains.

作者信息

Stojanovic A, Roher A E, Ball M J

机构信息

Department of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201.

出版信息

Dementia. 1994 Sep-Oct;5(5):229-33. doi: 10.1159/000106728.

Abstract

Using computer-enhanced image analysis, the amount of lipofuscin was measured in 500 hippocampal pyramidal neurons (regions CA2 and CA3) with and without neurofibrillary tangles (NFT), in brains of 10 patients with Alzheimer's disease (AD), as well as in 6 age-matched controls. The average content of lipofuscin in those cells from AD brains carrying NFT is only 10% of the total perikaryal area, whereas in the AD neurons free of NFT, and in age matched controls, lipofuscin amounted to 31 and 33% of cellular area, respectively. Measurements of lipofuscin's intrinsic autofluorescence confirmed this material to be three times more abundant in AD neurons without NFT and in controls. We propose that a breakdown in the capacity for making lipofuscin may result in the neuronal inability to store toxic waste. Such a defect could be responsible for the generation of NFT and ultimately may contribute to neuronal demise.

摘要

利用计算机增强图像分析技术,在10例阿尔茨海默病(AD)患者以及6例年龄匹配的对照者的大脑中,对500个有无神经原纤维缠结(NFT)的海马锥体神经元(CA2和CA3区)中的脂褐素含量进行了测量。携带NFT的AD脑区中那些细胞内脂褐素的平均含量仅占核周总面积的10%,而在无NFT的AD神经元以及年龄匹配的对照者中,脂褐素分别占细胞面积的31%和33%。对脂褐素固有自发荧光的测量证实,这种物质在无NFT的AD神经元和对照者中含量要多三倍。我们提出,脂褐素生成能力的破坏可能导致神经元无法储存有毒废物。这样一种缺陷可能是NFT产生的原因,最终可能导致神经元死亡。

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