Glutamate receptor activation is involved in 5-HT2 agonist-induced Arc gene expression in the rat cortex

Neuropharmacology. 2004 Mar;46(3):331-9. doi: 10.1016/j.neuropharm.2003.09.017.

Abstract

Brain 5-HT regulates the expression of gene transcription factor as well as novel effector immediate early genes (IEGs). The 5-HT regulation of the gene transcription factor IEG, c-fos, involves activation of 5-HT2A and ionotropic glutamate receptors. Here, we investigate whether these receptors are also involved in the regulation of the effector IEG, Arc. In rats, the 5-HT2 agonist DOI induced a marked increase in expression of Arc mRNA in a variety of cortical regions. This effect was blocked by the selective 5-HT2A receptor antagonist, MDL 100,907, but not the 5-HT(2B/2C) receptor antagonist, SB206553. The AMPA receptor antagonist GYKI 52466 also attenuated DOI-induced Arc mRNA expression, as did the NMDA receptor antagonist MK801 in some regions. Immunofluorescence studies showed that DOI increased Arc-immunoreactivity in cortical cells that expressed AMPA and NMDA receptor subunits but not the 5-HT2A receptor. Finally, DOI-induced Arc-immunoreactivity in cortical cells was extensively co-localised with c-fos-immunoreactivity. These results suggest that, as with c-fos expression, ionotropic glutamate receptors (AMPA and NMDA) are involved in 5-HT2A receptor-induced Arc expression. This finding, together with evidence of extensive Arc and c-fos co-localisation, suggests that 5-HT2A receptor activation may induce the expression of both effector and transcription factor IEGs via common molecular and cellular substrates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cerebral Cortex / drug effects*
  • Cerebral Cortex / metabolism*
  • Cytoskeletal Proteins
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology
  • Immediate-Early Proteins / biosynthesis*
  • Immediate-Early Proteins / genetics
  • Male
  • Nerve Tissue Proteins*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Glutamate / metabolism*
  • Serotonin Antagonists / pharmacology
  • Serotonin Receptor Agonists / pharmacology*

Substances

  • Cytoskeletal Proteins
  • Immediate-Early Proteins
  • Nerve Tissue Proteins
  • Receptors, Glutamate
  • Serotonin Antagonists
  • Serotonin Receptor Agonists
  • activity regulated cytoskeletal-associated protein