Premium
Distinct gene expression signatures in the striata of wild‐type and heterozygous c‐fos knockout mice following methamphetamine administration: Evidence from cDNA array analyses
Author(s) -
Cadet Jean Lud,
McCoy Michael T.,
Ladenheim Bruce
Publication year - 2002
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.10074
Subject(s) - meth , methamphetamine , gene knockout , knockout mouse , monoaminergic , neurotoxin , biology , gene , gene expression , microbiology and biotechnology , apoptosis , downregulation and upregulation , pharmacology , genetics , chemistry , endocrinology , serotonin , receptor , monomer , organic chemistry , acrylate , polymer
Methamphetamine (METH) is a drug of abuse which can cause apoptosis and degeneration of monoaminergic terminals in the mammalian brain. c‐fos appears to play a protective role against METH‐induced damage because METH toxicity is exacerbated in c‐fos heterozygous knockout mice. In the present study, we used the comprehensive technique of cDNA array to test the idea that heterozygous c‐fos knockout mice might show differential METH‐induced molecular responses in comparison to wild‐type (WT) animals. Of 1,176 genes examined, the expression of 195 genes in either of the two groups of mice was affected by at least 2‐fold at 2 or 12 h after METH treatment. More genes were either up‐ or downregulated in the WT mice. Moreover, there were substantial differences in the pattern of responses between the two genotypes, with more genes involved in DNA repair and protective processes being upregulated in WT mice after METH administration. These results support the idea that the c‐fos knockout genotype may render the animals unable to trigger multicomponent responses in order to protect against the multifaceted toxic effects of this illicit neurotoxin. Synapse 44:211–226, 2002. © 2002 Wiley‐Liss, Inc.