Mitochondrial abnormalities in Alzheimer's disease

被引:1112
|
作者
Hirai, K
Aliev, G
Nunomura, A
Fujioka, H
Russell, RL
Atwood, CS
Johnson, AB
Kress, Y
Vinters, HV
Tabaton, M
Shimohama, S
Cash, AD
Siedlak, SL
Harris, PLR
Jones, PK
Petersen, RB
Perry, G
Smith, MA
机构
[1] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Neurol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[4] Takeda Chem Ind Ltd, Pharmaceut Res Labs 1, Osaka 5328686, Japan
[5] Takeda Chem Ind Ltd, Div Pharmaceut Res, Osaka 5328686, Japan
[6] Asahikawa Med Coll, Dept Psychiat & Neurol, Asahikawa, Hokkaido 0788510, Japan
[7] Yeshiva Univ Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[8] Univ Calif Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA 90024 USA
[9] Univ Genoa, Dept Neurosci, I-16132 Genoa, Italy
[10] Kyoto Univ, Dept Neurol, Kyoto 6068507, Japan
来源
JOURNAL OF NEUROSCIENCE | 2001年 / 21卷 / 09期
关键词
Alzheimer's disease; free radicals; metabolism; mitochondria; neurodegeneration; oxidative stress;
D O I
10.1523/JNEUROSCI.21-09-03017.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The finding that oxidative damage, including that to nucleic acids, in Alzheimer's disease is primarily limited to the cytoplasm of susceptible neuronal populations suggests that mitochondrial abnormalities might be part of the spectrum of chronic oxidative stress of Alzheimer's disease. In this study, we used in situ hybridization to mitochondrial DNA (mtDNA), immunocytochemistry of cytochrome oxidase, and morphometry of electron micrographs of biopsy specimens to determine whether there are mitochondrial abnormalities in Alzheimer's disease and their relationship to oxidative damage marked by 8-hydroxyguanosine and nitrotyrosine. We found that the same neurons showing increased oxidative damage in Alzheimer's disease have a striking and significant increase in mtDNA and cytochrome oxidase. Surprisingly, much of the mtDNA and cytochrome oxidase is found in the neuronal cytoplasm and in the case of mtDNA, the vacuoles associated with lipofuscin. Morphometric analysis showed that mitochondria are significantly reduced in Alzheimer's disease. The relationship shown here between the site and extent of mitochondrial abnormalities and oxidative damage suggests an intimate and early association between these features in Alzheimer's disease.
引用
收藏
页码:3017 / 3023
页数:7
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