Disruption of zinc homeostasis in Alzheimer's disease

被引:11
作者
Robertson, JD [1 ]
Crafford, AM
Markesbery, WR
Lovell, MA
机构
[1] Univ Missouri, Dept Chem, Columbia, MO 65211 USA
[2] Univ Kentucky, Dept Neurol, Lexington, KY 40536 USA
[3] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
[4] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[5] Univ Missouri, Missouri Res Reactor, Columbia, MO 65211 USA
[6] Univ Kentucky, Dept Pathol, Lexington, KY 40536 USA
关键词
zinc; brain; Alzheimer's disease; micro-PIXE; LA-ICP-MS;
D O I
10.1016/S0168-583X(01)01124-7
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The basic hypothesis being tested is that, in Alzheimer's disease (AD), the delicate balance of brain Zn is disrupted and may play a role in the pathogenesis of neuron degeneration. Micro-PIXE measurements reveal a significant elevation of Zn in senile plaques (SP) in AD brain compared with adjacent neuropil and a significant increase in AD neuropil compared to control neuropil. The observation of elevated Zn in SP is of interest because the amyloid precursor protein contains a Zn binding site that may prevent normal cleavage leading to the generation of a toxic fragment of beta amyloid, the constituent of SP, The potential of using laser-ablation inductively coupled plasma mass spectrometry as a complimentary microprobe technique is also presented. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:454 / 458
页数:5
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