Etienne P, Robitaille Y, Wood P, Gauthier S, Nair N P, Quirion R
Neuroscience. 1986 Dec;19(4):1279-91. doi: 10.1016/0306-4522(86)90142-9.
All our advanced, severe cases of Alzheimer's disease have dramatic cholinergic cell losses in the nucleus basalis of Meynert even after correction for cell or nucleoli shrinkage. There is a good correlation between choline acetyltransferase activity and "healthy" cell number in the nucleus basalis of Meynert. Half of the Alzheimer disease cases have markedly reduced cortical choline acetyltransferase activity in spite of preserved nucleus basalis of Meynert choline acetyltransferase activity, suggesting a deficiency of cortical origin and/or of axonal transport in Alzheimer disease. The relationship between cell loss in the various sub-divisions of the nucleus basalis of Meynert and plaque counts in corresponding and non-corresponding projection areas of the cortex has also been examined. Globally, this relation appears more obvious when cell loss in a sub-division of the nucleus basalis of Meynert is compared to plaque counts in its cortical projection area. However, the relation is discontinuous with few or no data to document the intermediary stages of the process, probably reflecting the severity of our Alzheimer disease cases.
我们所有晚期重度阿尔茨海默病患者,即使在对细胞或核仁萎缩进行校正后,其Meynert基底核中胆碱能细胞仍有显著丢失。胆碱乙酰转移酶活性与Meynert基底核中的“健康”细胞数量之间存在良好的相关性。尽管Meynert基底核胆碱乙酰转移酶活性保持正常,但半数阿尔茨海默病患者的皮质胆碱乙酰转移酶活性显著降低,这表明阿尔茨海默病存在皮质起源缺陷和/或轴突运输缺陷。研究人员还检测了Meynert基底核各个亚区的细胞丢失与皮质相应及非相应投射区域的斑块计数之间的关系。总体而言,将Meynert基底核一个亚区的细胞丢失与其皮质投射区域的斑块计数进行比较时,这种关系似乎更为明显。然而,这种关系并不连续,几乎没有数据记录该过程的中间阶段,这可能反映了我们所研究的阿尔茨海默病病例的严重程度。