Geula C, Mesulam M M
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Alzheimer Dis Assoc Disord. 1995;9 Suppl 2:23-8. doi: 10.1097/00002093-199501002-00005.
Alzheimer disease (AD) is accompanied by a marked loss of acetylcholinesterase (AChE) activity associated with cortical cholinergic axons and cholinoceptive neurons. Simultaneous with this loss, cholinesterase (ChE) activity emerges in AD cortex in the form of AChE and butyrylcholinesterase activity associated with plaques, tangles, and amyloid angiopathy. Our observations have shown that the ChEs associated with the pathological lesions of AD (ADChEs) possess different enzymatic properties and quite possibly are of a different source as compared with the ChEs associated with normal neurons and axons. The ADChEs most likely have noncholinergic functions involved in the pathogenesis of AD. The postulated functions include acting as proteases/peptidases, participating directly in the amyloidogenic processing of the amyloid precursor protein, and causing aberrant growth of neuronal processes. The therapeutic and diagnostic implications of ADChEs are discussed.
阿尔茨海默病(AD)伴随着与皮质胆碱能轴突和胆碱能感受神经元相关的乙酰胆碱酯酶(AChE)活性显著丧失。与此同时,胆碱酯酶(ChE)活性以与斑块、缠结和淀粉样血管病相关的AChE和丁酰胆碱酯酶活性的形式出现在AD皮质中。我们的观察表明,与AD病理病变相关的ChE(ADChE)具有不同的酶学特性,并且与正常神经元和轴突相关的ChE相比,很可能来源不同。ADChE最有可能具有参与AD发病机制的非胆碱能功能。推测的功能包括作为蛋白酶/肽酶,直接参与淀粉样前体蛋白的淀粉样生成过程,并导致神经元突起异常生长。本文讨论了ADChE在治疗和诊断方面的意义。