MK-801 inhibits the induction of immediate early genes in cerebral cortex, thalamus, and hippocampus, but not in substantia nigra following middle cerebral artery occlusion

Neurosci Lett. 1994 Sep 26;179(1-2):111-4. doi: 10.1016/0304-3940(94)90947-4.

Abstract

Middle cerebral artery (MCA) occlusion in rats induced c-fos and junB mRNA 4h later in all ipsilateral cortex outside the MCA distribution and in many subcortical structures: medial striatum; most of thalamus including medial and lateral geniculate nuclei: substantia nigra; and hippocampus. The N-methyl-D-aspartate (NMDA) antagonist, MK-801 (4 mg/kg, i.p.) inhibited c-fos and junB mRNA induction in the cortex, striatum, thalamus, and hippocampus but not in the substantia nigra. These data show that c-fos and junB mRNA induction in cortex, striatum, thalamus, hippocampus involves the activation of NMDA receptors whereas different receptors must be implicated in the induction in substantia nigra.

MeSH terms

  • Animals
  • Brain Chemistry / drug effects*
  • Brain Ischemia / metabolism*
  • Cerebral Arteries / physiology
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism
  • Dizocilpine Maleate / pharmacology*
  • Gene Expression / drug effects*
  • Genes, Immediate-Early / drug effects*
  • Genes, fos / drug effects
  • Genes, jun / drug effects
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Male
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Substantia Nigra / drug effects
  • Substantia Nigra / metabolism
  • Thalamus / drug effects
  • Thalamus / metabolism

Substances

  • RNA, Messenger
  • Dizocilpine Maleate