Early and late gene changes in MPTP mice model of Parkinson's disease employing cDNA microarray

被引:55
作者
Mundel, S
Grünblatt, E
Maor, G
Youdim, MBH
机构
[1] Technion Israel Inst Technol, Fac Med, Dept Pharmacol, IL-31096 Haifa, Israel
[2] Bruce Rappaport Family Res Inst, Eve Topf Parkinsons Fdn, Ctr Excellence Neurodegenerat Dis, Haifa, Israel
[3] Bruce Rappaport Family Res Inst, US Natl Parkinsons Fdn, Ctr Excellence Neurodegenerat Dis, Haifa, Israel
[4] Univ Wurzburg, Dept Neurochem, Clin & Polyclin Psychiat & Psychotherapy, Wurzburg, Germany
关键词
cDNA microarray; Parkinson's disease; MPTP; oxidative-stress; neurodegeneration; gene expression;
D O I
10.1023/A:1020989812576
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
Recently, we reported specific brain gene expression changes in the chronic MPTP model in the late stage of degeneration, employing cDNA expression array, which indicate a "domino" cascade of events involved in neuronal cell death. In an attempt to elucidate early gene expression profile in the region of the substantia nigra (SN) and the striatum of acute MPTP-treated mice (3-24 h), we elected a restricted number of genes affected by the long-term MPTP treatment, and their expression was examined. Specifically, we detected alterations in the expression of genes implicated in oxidative-stress, inflammatory processes, signal transduction and glutamate toxicity. These pro-toxic genes appear to be compensated by the elevated expression in trophic factors and antioxidant defenses, which are also activated by short exposure to MPTP. The time course of these gene expression changes indicates the importance of investigating the early gene cascade of events occurring prior to late nigrostriatal dopamine neuronal cell death.
引用
收藏
页码:1231 / 1243
页数:13
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