D2 dopamine receptor but not AMPA and kainate glutamate receptor genes show altered expression in response to long term treatment with trans- and cis-flupenthixol in the rat brain

Brain Res Mol Brain Res. 1999 May 7;68(1-2):14-21. doi: 10.1016/s0169-328x(99)00037-6.

Abstract

Glutamate receptor function has been hypothesized as an important factor in both the aetiology and treatment of schizophrenia. We have used a multiprobe oligonucleotide solution hybridization (MOSH) technique to examine the regulation of gene expression of the GluR1-7, KA1, and KA2 glutamate receptor subunits in the left rat brain following treatment with the optical isomers of flupenthixol at a dose of 0.2 mg kg-1 day-1 over a period of 4, 12, 24 weeks in order to understand how specific glutamate receptor genes are involved in the treatment of schizophrenia. The GluR2/3 and GluR6/7 subunit immunoreactivity in the right brain following 4 and 24 weeks of drug treatment was also examined by Western blotting. Neither trans- nor cis-flupenthixol was found to alter the gene expression of any of the 9 non-NMDA glutamate receptor subunits. On the other hand, we found a nearly two-fold increase in gene expression of the D2 dopamine receptor in specific brain regions. These results suggest that non-NMDA types of glutamate receptor subunits, in contrast to NMDA receptors, are less likely to have a role in the action of antipsychotic drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antipsychotic Agents / pharmacology*
  • Brain / drug effects*
  • Brain / metabolism
  • Dopamine Antagonists / pharmacology*
  • Flupenthixol / pharmacology
  • Gene Expression Regulation / drug effects*
  • Male
  • Molecular Sequence Data
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, AMPA / genetics
  • Receptors, Dopamine D2 / genetics*
  • Receptors, Glutamate / genetics*
  • Receptors, Kainic Acid / genetics
  • Stereoisomerism
  • Time Factors

Substances

  • Antipsychotic Agents
  • Dopamine Antagonists
  • Receptors, AMPA
  • Receptors, Dopamine D2
  • Receptors, Glutamate
  • Receptors, Kainic Acid
  • Flupenthixol