NAD(P)H:quinone oxidoreductase activity is increased in hippocampal pyramidal neurons of patients with Alzheimer's disease

被引:75
作者
Wang, YX
Santa-Cruz, K
DeCarli, C
Johnson, JA
机构
[1] Dept Pharmacol Toxicol & Therapeut, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66160 USA
[3] Univ Kansas, Med Ctr, Dept Pathol, Kansas City, KS 66160 USA
[4] Univ Kansas, Med Ctr, Alzheimers Dis Ctr, Kansas City, KS 66160 USA
[5] Univ Kansas, Med Ctr, Mental Retardat Res Ctr, Kansas City, KS 66160 USA
[6] Univ Kansas, Med Ctr, Ctr Environm & Occupat Hlth, Kansas City, KS 66160 USA
关键词
Alzheimer's disease; NAD(P)H : quinone oxidoreductase; neurons; oxidative stress;
D O I
10.1016/S0197-4580(00)00114-7
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
NAD(P)H:quinone oxidoreductase (QR) catalyzes the two-electron reduction of quinones, preventing their participation in redox cycling and subsequent generation of reactive oxygen species. Pretreatment of neuroblastoma cells with compounds, such as tert-butylhydroquinone and dimethyl fumarate, that increase QR expression protect cells from oxidative stress-induced cell death by glutamate, H2O2 and dopamine. The potential neuroprotective role of QR as well as the evidence for oxidative stress-induced neuronal cell death in Alzheimer's disease (AD) led us to examine the expression pattern of QR from AD and control patients. Histochemical staining of hippocampal sections from AD patients revealed QR activity in pyramidal neurons. The presence of QR protein in these neurons also was confirmed by immunoreactivity, In control patients, hippocampal pyramidal neurons were negative for both QR enzymatic activity and QR immunoreactivity. In addition, the QR positive neurons of AD patients were selectively located in areas where neuronal populations exhibited tau immunostaining. Our data demonstrate that QR is up-regulated in hippocampal pyramidal neurons of AD patients. We hypothesize that this is part of a neuroprotective system up-regulated in response to the AD process. Understanding this system may lead to further insights into the pathogenesis and potential new avenues of treatment for AD. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:525 / 531
页数:7
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