In vivo study of acetylcholine esterase in basal forebrain, amygdala, and cortex in mild to moderate Alzheimer disease

被引:96
作者
Herholz, K
Weisenbach, S
Zündorf, G
Lenz, O
Schröder, H
Bauer, B
Kalbe, E
Heiss, WD
机构
[1] Univ Cologne, Neurol Klin, D-50931 Cologne, Germany
[2] Max Planck Inst Neurol Res, D-50931 Cologne, Germany
[3] Univ Cologne, Dept Anat Neuroanat 2, Cologne, Germany
关键词
Alzheimer disease; nucleus basalis Meynert; acetylcholine esterase; cerebral glucose metabolism; positron emission tomography; amygdala;
D O I
10.1016/j.neuroimage.2003.09.042
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is currently unclear whether impairment of the cholinergic system is present in Alzheimer disease (AD) already at an early stage and to what extent it depends on degeneration of the nucleus basalis of Meynert (nbM). We examined acetylcholine esterase activity in vivo in the nbM, the amygdala, and cerebral neocortex. Measurements were performed in normal controls and in patients with mild to moderate AD with positron emission tomography (PET) and C-11-labeled N-methyl-4-piperidyl-acetate (MP4A) which is a specific substrate of AChE. AChE activity was reduced significantly in amygdala and cerebral cortex. In contrast, AChE activity and glucose metabolism appeared preserved or even increased in the nbM. The results support the concept that neocortical and amygdaloid functional changes of the cholinergic system are an early and leading event in AD, rather than the consequence of neurodegeneration of basal nuclei. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:136 / 143
页数:8
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