Lawrence A D, Sahakian B J
Department of Psychiatry, University of Cambridge, UK.
Neurochem Res. 1998 May;23(5):787-94. doi: 10.1023/a:1022419712453.
The primary pathology in Alzheimer's disease (DAT) occurs in the basal forebrain cholinergic system (BFCS), which provides the major cholinergic innervation to the neocortex, hippocampus and amygdala. Consistent with the 'cholinergic hypothesis' of dementia in DAT, the most effective treatments so far developed for DAT are drugs which act to boost the functions of the BFCS. These include the centrally acting cholinesterase inhibitor tacrine, and the cholinergic agonist nicotine, acute administration of which leads to an improvement in attentional functions, in line with recent animal studies of the role of the BFCS in cognition. We conclude that future research should include the development of more potent, longer-lasting, less toxic cholinergic agents, which appear to be the best candidates for alleviating the cognitive symptomatology of DAT. Such drugs may also be useful in the treatment of a number of other cognitive disorders, including Lewy body dementia, attention deficit/hyperactivity disorder, and schizophrenia.
阿尔茨海默病(DAT)的主要病理变化发生在基底前脑胆碱能系统(BFCS),该系统为新皮层、海马体和杏仁核提供主要的胆碱能神经支配。与DAT痴呆的“胆碱能假说”一致,迄今为止针对DAT开发的最有效的治疗方法是作用于增强BFCS功能的药物。这些药物包括中枢作用的胆碱酯酶抑制剂他克林,以及胆碱能激动剂尼古丁,急性给予尼古丁会改善注意力功能,这与最近关于BFCS在认知中作用的动物研究结果一致。我们得出结论,未来的研究应包括开发更有效、作用更持久、毒性更小的胆碱能药物,这些药物似乎是缓解DAT认知症状的最佳候选药物。此类药物也可能有助于治疗其他一些认知障碍,包括路易体痴呆、注意力缺陷多动障碍和精神分裂症。