Rogers J, Morrison J H
J Neurosci. 1985 Oct;5(10):2801-8. doi: 10.1523/JNEUROSCI.05-10-02801.1985.
Senile (neuritic) plaques are one of the two major neuropathologic hallmarks of Alzheimer's disease. Despite their obvious importance (e.g., they are significantly correlated with severity of dementia), there is little present information about their etiology, the specific neuronal elements that form them, or a quantitative definition of where in cortex they occur. We have sought clues to these issues by quantifying regional and laminar distributions of neocortical plaques and setting these data against the present wealth of information on neocortical cytoarchitecture and neurotransmitter-specific circuitry. Senile plaques are significantly more numerous in associative regions of neocortex than in sensory areas and are significantly more numerous in cortical laminae dominated by their role in corticocortical, associative relations. Plaques are also largest in those laminae characterized by large pyramidal cells subserving input/output functions. The quantitative distribution of senile plaques in Alzheimer's disease does not necessarily correspond to innervation patterns for any known subcortical afferent system. This, coupled with the finding that several different neurotransmitters can be immunocytochemically co-localized with plaques, casts doubts on a primary role of cholinergic deterioration in plaque etiology, and opens the possibility that neocortical senile plaques may derive from pathologic events initiated in the neocortex.
老年(神经炎性)斑是阿尔茨海默病两大主要神经病理学特征之一。尽管它们具有明显的重要性(例如,它们与痴呆严重程度显著相关),但目前关于其病因、形成它们的特定神经元成分或其在皮质中出现位置的定量定义的信息很少。我们通过量化新皮质斑的区域和层状分布,并将这些数据与目前关于新皮质细胞结构和神经递质特异性回路的丰富信息进行对比,来寻找这些问题的线索。老年斑在新皮质的联合区域比在感觉区域明显更多,并且在以其在皮质 - 皮质联合关系中的作用为主导的皮质层中明显更多。斑在以具有执行输入/输出功能的大锥体细胞为特征的那些层中也最大。阿尔茨海默病中老年斑的定量分布不一定与任何已知皮质下传入系统的神经支配模式相对应。这一点,再加上几种不同神经递质可与斑免疫细胞化学共定位这一发现,使人对胆碱能退化在斑病因中的主要作用产生怀疑,并开启了新皮质老年斑可能源自新皮质中引发的病理事件的可能性。