Arendt T, Bigl V, Tennstedt A, Arendt A
Neuroscience. 1985 Jan;14(1):1-14. doi: 10.1016/0306-4522(85)90160-5.
In order to substantiate the hypothesis of a cholinergic pathogenesis of neuritic plaques in Alzheimer's disease the relationship between the loss of cholinergic neurons in six subdivisions of the nucleus basalis of Meynert and density of neuritic plaques in five neocortical target areas and hippocampus was studied in five cases with Alzheimer's disease. Distribution of plaques in different cortical areas as well as degeneration pattern of neurons within the subpopulations of the nucleus basalis were markedly different in the cases of Alzheimer's disease. Quantitative evaluation of the number of neuritic plaques in the five cortical areas revealed a strong correlation with the loss of neurons in those subpopulations of the nucleus basalis which give rise to the cholinergic innervation of the affected cortical areas. The nonlinearity of this correlation may reflect two different modes of plaque formation. Either plaque formation is a self-perpetuating process with an increasing rate depending on the number of plaques already formed or additional mechanisms, with an increasing rate of influence during plaque formation are induced. The shape of the regression function is different for the various cortical regions and their corresponding subpopulations of the nucleus basalis suggesting a different dependency of neuritic plaque formation on the neuronal loss in the nucleus basalis. This might reflect a different density of cholinergic fibers within these areas, a different degree of collateralization of the fibers or other factors not yet known. The findings indicate that degeneration of cortical cholinergic afferents from the neurons of the nucleus basalis is an important feature in the pathogenesis of neuritic plaques.
为了证实阿尔茨海默病中神经炎性斑块胆碱能发病机制的假说,我们研究了5例阿尔茨海默病患者中,Meynert基底核六个亚区胆碱能神经元的丧失与五个新皮质靶区及海马中神经炎性斑块密度之间的关系。在阿尔茨海默病患者中,不同皮质区域斑块的分布以及基底核亚群内神经元的变性模式明显不同。对五个皮质区域神经炎性斑块数量的定量评估显示,其与基底核中那些为受影响皮质区域提供胆碱能神经支配的亚群中神经元的丧失密切相关。这种相关性的非线性可能反映了斑块形成的两种不同模式。要么斑块形成是一个自我延续的过程,其速率随着已形成斑块数量的增加而增加,要么是在斑块形成过程中诱导了其他机制,且其影响速率也在增加。不同皮质区域及其对应的基底核亚群的回归函数形状不同,这表明神经炎性斑块形成对基底核神经元丧失的依赖性不同。这可能反映了这些区域内胆碱能纤维的不同密度、纤维的不同侧支化程度或其他未知因素。研究结果表明,基底核神经元的皮质胆碱能传入纤维变性是神经炎性斑块发病机制中的一个重要特征。