Hamos J E, DeGennaro L J, Drachman D A
Department of Neurology, University of Massachusetts Medical Center, Worcester 01655.
Neurology. 1989 Mar;39(3):355-61. doi: 10.1212/wnl.39.3.355.
The extent and location of neuronal losses necessary or sufficient to produce dementia in patients with Alzheimer's Disease (AD) is unknown. To approach this question, we studied synaptic terminals in postmortem brain tissue utilizing immunohistochemical techniques. We used antibodies against two proteins found in synaptic terminals--synapsin I and synaptophysin--as synaptic markers in the hippocampal complexes of eight patients with autopsy-proven AD and eight nondemented control subjects. Quantitative microscopy measured the regional density of synaptic staining. All AD patients showed a striking decrease in synaptic staining in the outer half of the molecular layer of the dentate gyrus compared with control brains, where the density of synaptic terminals was uniform throughout. In an additional patient with progressive degenerative dementia but without plaques or tangles on neuropathologic examination, similar depletion of synaptic staining was seen in the dentate gyrus. Quantitative densitometric analyses confirmed the focal decrease in synaptic staining in the outer half of the molecular layer in demented patients. We also found a slight increase in synaptic staining in the inner half of this layer.
在阿尔茨海默病(AD)患者中,导致痴呆所需或足以导致痴呆的神经元损失的程度和位置尚不清楚。为了解决这个问题,我们利用免疫组织化学技术研究了死后脑组织中的突触终末。我们使用针对在突触终末发现的两种蛋白质——突触素I和突触囊泡蛋白——的抗体,作为8例经尸检证实为AD的患者和8例非痴呆对照受试者海马复合体中的突触标记物。定量显微镜测量突触染色的区域密度。与对照脑相比,所有AD患者齿状回分子层外半部分的突触染色均显著减少,对照脑中突触终末的密度在整个区域是均匀的。在另一例进行性退行性痴呆患者中,神经病理学检查未发现斑块或缠结,但在齿状回中也观察到类似的突触染色减少。定量密度分析证实了痴呆患者分子层外半部分突触染色的局灶性减少。我们还发现该层内半部分的突触染色略有增加。