Mesulam M M, Geula C
Division of Neuroscience and Behavioral Neurology, Harvard Medical School, Boston, Massachusetts.
J Comp Neurol. 1988 Sep 8;275(2):216-40. doi: 10.1002/cne.902750205.
The nucleus basalis (NB) of the human brain is a large, complex, and highly differentiated structure. Many of its neurons are magnocellular, hyperchromic, isodendritic, acetylcholinesterase-rich, and choline-acetyltransferase-positive. Concurrent histochemical and immunological staining demonstrated that all choline-acetyltransferase-positive NB neurons in the human brain also contain acetylcholinesterase enzyme activity. Only a small minority of acetylcholinesterase-rich magnocellular cell bodies in the NB failed to show choline acetyltransferase immunoreactivity. Sections that were counterstained for Nissl substance showed that 80-90% of all magnocellular neurons in the NB were choline-acetyltransferase-positive and therefore cholinergic. These characteristics, which are very similar to those of the NB in the monkey brain, justified the designation of these cholinergic neurons in the human brain as the Ch4 (or NB-Ch4) complex. On morphological grounds, the compact parts of the human NB-Ch4 complex were divided into distinct sectors which appeared to show a greater level of differentiation than in the monkey brain. In addition to the compact sectors, interstitial elements of NB Ch4 were embedded within adjacent fiber bundles. The putative cortical projections from NB-Ch4 were identified in the form of acetylcholinesterase-rich fibers. These fibers formed a dense plexus in all cortical regions but also displayed laminar and regional variations. Limbic and paralimbic areas had higher concentrations of these fibers than the immediately adjacent neocortical association areas. Alzheimer's disease was associated with a marked depletion of cortical acetylcholinesterase. Two cases of Alzheimer's disease with relatively selective NB-Ch4 cell loss supported the hypothesis that the corticopetal cholinergic pathways in the human brain may have a topographical organization similar to that in the monkey brain.
人脑的基底核(NB)是一个大型、复杂且高度分化的结构。其许多神经元是大细胞性、嗜染质增多、等树突状、富含乙酰胆碱酯酶且胆碱乙酰转移酶呈阳性的。同时进行的组织化学和免疫染色表明,人脑中所有胆碱乙酰转移酶呈阳性的NB神经元也都含有乙酰胆碱酯酶活性。NB中仅一小部分富含乙酰胆碱酯酶的大细胞胞体未显示胆碱乙酰转移酶免疫反应性。用尼氏物质进行复染的切片显示,NB中所有大细胞神经元的80 - 90%是胆碱乙酰转移酶呈阳性的,因此是胆碱能的。这些与猴脑NB非常相似的特征,为人脑中这些胆碱能神经元被命名为Ch4(或NB - Ch4)复合体提供了依据。基于形态学原因,人NB - Ch4复合体的致密部分被分为不同的区域,这些区域似乎比猴脑表现出更高程度的分化。除了致密区域外,NB Ch4的间质成分嵌入相邻的纤维束中。来自NB - Ch4的假定皮质投射以富含乙酰胆碱酯酶的纤维形式被识别。这些纤维在所有皮质区域形成密集的丛,但也表现出层状和区域差异。边缘和边缘旁区域这些纤维的浓度高于紧邻的新皮质联合区域。阿尔茨海默病与皮质乙酰胆碱酯酶的显著减少有关。两例具有相对选择性NB - Ch4细胞丢失的阿尔茨海默病病例支持了这样的假说,即人脑中向皮质的胆碱能通路可能具有与猴脑相似的拓扑组织。