Neurotransmitter deficits in Alzheimer's disease and in other dementing disorders.

Human neurobiology Pub Date : 1986-01-01
D M Mann, P O Yates
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Abstract

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.

阿尔茨海默病和其他痴呆症的神经递质缺陷。
综述了阿尔茨海默病中神经递质缺乏的证据。以乙酰胆碱、去甲肾上腺素和血清素为基础的皮层下传入投射系统发生重大损失。在皮层中,含有生长抑素的神经元和大锥体细胞是受损最严重的细胞,它们被认为使用谷氨酸/天冬氨酸作为递质。如果损伤的原发部位位于皮层内,细胞损失的解剖分布是可以解释的;神经细胞由于在这个区域内或与这个区域的连接而受损。老年斑可能代表这种损伤的部位,神经原纤维缠结的形成和积累可能导致细胞死亡。活过40岁的唐氏综合症患者体内的递质变化与阿尔茨海默氏症患者明显相同。帕金森病的痴呆似乎与胆碱能、去甲肾上腺素能和多巴胺能系统的损伤有关,可能反映了这些皮层下区域未能充分“激活”原本未受损的皮层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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