Microarray analysis of gene expression in rat hippocampus after chronic ethanol treatment

被引:65
作者
Saito, M
Smiley, J
Toth, R
Vadasz, C
机构
[1] Nathan S Kline Inst Psychiat Res, Lab Neurobehav Genet, Orangeburg, NY 10962 USA
[2] NYU, Med Ctr, New York, NY 10016 USA
[3] Nathan S Kline Inst Psychiat Res, Program Cognit Neurol & Schizophrenia, Orangeburg, NY 10962 USA
关键词
chronic ethanol; high-density cDNA array; gene expression; hippocampus;
D O I
10.1023/A:1020937728506
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is thought that changes in gene expression in the brain mediate chronic ethanol-induced complex behaviors such as tolerance, dependence, and sensitization, and also relate to ethanol-induced brain toxicity. Using high-density filter-based cDNA microarrays (GeneFilters), we analyzed the expression of over 5000 genes in the dorsal hippocampus of rats treated with 12% ethanol or tap water for 15 months. Ethanol-induced changes in gene expression were particularly prominent in two groups of genes. One group consisted of oxidoreductases, including ceruloplasmin, uricase, branched-chain alpha-keto acid dehydrogenase, NADH ubiquinone oxidoreductase, P450, NAD(+)-isocitrate dehydrogenase, and cytochrome c oxidase, which may be related to ethanol-induced oxidative stress. The other group of genes included ADP-ribosylation factor, RAS related protein rab10, phosphatidylinositol 4-kinase, dynein-associated polypeptides, and dynamin-1, which seem to be involved in membrane trafficking. The results may reveal some of the pathways involved in ethanol-induced pathophysiological changes.
引用
收藏
页码:1221 / 1229
页数:9
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