Mann D M, Yates P O
Hum Neurobiol. 1986;5(3):147-58.
The evidence for deficiencies in neurotransmitters in Alzheimer's disease is reviewed. Major losses occur in the subcortical afferent projection systems based on acetylcholine, noradrenaline and serotonin. Within the cortex, somatostatin containing neurones and the large pyramidal cells, presumed to use glutamate/aspartate as transmitters, are the most severely damaged cells. The anatomical distribution of cell loss is explainable if the primary site of damage lies within the cortex; nerve cells are damaged by virtue of their presence within or their connections to this region. The senile plaque may represent the site of this damage and neurofibrillary tangle formation and accumulation may lead to cell death. In patients with Down's syndrome who live past 40 years, changes in transmitters apparently identical to those in Alzheimer's disease occur. The dementia of Parkinson's disease appears related to damage to cholinergic, noradrenergic and dopaminergic systems and may reflect a failure of these subcortical regions to sufficiently "activate" an otherwise undamaged cortex.
本文综述了阿尔茨海默病中神经递质缺乏的证据。基于乙酰胆碱、去甲肾上腺素和5-羟色胺的皮质下传入投射系统出现重大损失。在皮质内,含有生长抑素的神经元和被认为以谷氨酸/天冬氨酸为递质的大锥体细胞是受损最严重的细胞。如果损伤的主要部位在皮质内,那么细胞丢失的解剖分布是可以解释的;神经细胞因其存在于该区域内或与该区域的连接而受损。老年斑可能代表了这种损伤的部位,神经原纤维缠结的形成和积累可能导致细胞死亡。在活到40岁以上的唐氏综合征患者中,明显出现了与阿尔茨海默病中相同的递质变化。帕金森病性痴呆似乎与胆碱能、去甲肾上腺素能和多巴胺能系统的损伤有关,可能反映了这些皮质下区域未能充分“激活”原本未受损的皮质。