Chronic treatment with aripiprazole induces differential gene expression in the rat frontal cortex

Int J Neuropsychopharmacol. 2008 Mar;11(2):207-16. doi: 10.1017/S1461145707008048. Epub 2007 Sep 17.

Abstract

Chronic treatment of antipsychotic drugs can modulate gene expression in the brain, which may underscore their clinical efficacy. Aripiprazole is the first approved antipsychotic drug of the class of dopamine D2 receptor partial agonist, which has been shown to have similar efficacy and favourable side-effects profile compared to other antipsychotic drugs. This study aimed to identify differential gene expression induced by chronic treatment of aripiprazole. We used microarray-based gene expression profiling technology, real-time quantitative PCR and Western blot analysis to identify differentially expressed genes in the frontal cortex of rats under 4 wk treatment of aripiprazole (10 mg/kg). We were able to detect ten up-regulated genes, including early growth response gene 1, 2, 4 (Egr1, Egr2, Egr4), chromobox homolog 7 (Cbx7), cannabinoid receptor (Cnr1), catechol-O-methyltransferase (Comt), protein phosphatase 2c, magnesium dependent (Ppm2c), tachykinin receptor 3 (Tacr3), Wiscott-Aldrich syndrome-like gene (Wasl) and DNA methyltransferase 3a (Dnmt3a). Our data indicate that chronic administration of aripiprazole can induce differential expression of genes involved in transcriptional regulation and chromatin remodelling and genes implicated in the pathogenesis of psychosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antipsychotic Agents / pharmacology*
  • Aripiprazole
  • Blotting, Western
  • Cerebral Cortex / drug effects*
  • Cerebral Cortex / metabolism
  • Gene Expression Profiling* / methods
  • Male
  • Oligonucleotide Array Sequence Analysis
  • Piperazines / pharmacology*
  • Quinolones / pharmacology*
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transcription, Genetic / drug effects*

Substances

  • Antipsychotic Agents
  • Piperazines
  • Quinolones
  • RNA, Messenger
  • Aripiprazole