SPATIOTEMPORAL INDUCTION OF IMMEDIATE-EARLY GENES IN THE RAT-BRAIN AFTER LIMBIC SEIZURES - EFFECTS OF NMDA RECEPTOR ANTAGONIST MK-801

Citation
P. Gass et al., SPATIOTEMPORAL INDUCTION OF IMMEDIATE-EARLY GENES IN THE RAT-BRAIN AFTER LIMBIC SEIZURES - EFFECTS OF NMDA RECEPTOR ANTAGONIST MK-801, European journal of neuroscience, 5(7), 1993, pp. 933-943
Citations number
89
Categorie Soggetti
Neurosciences
ISSN journal
0953816X
Volume
5
Issue
7
Year of publication
1993
Pages
933 - 943
Database
ISI
SICI code
0953-816X(1993)5:7<933:SIOIGI>2.0.ZU;2-Q
Abstract
Fos, jun and krox belong to multigene families coding for transcriptio n factors. These cellular immediate early genes (IEGs) are thought to be involved in coupling neuronal excitation to changes of target gene expression. Immunocytochemistry with specific antisera was used to ass ess regional levels of six IEG-encoded proteins (c-Fos, Fos B, Krox-24 , c-Jun, Jun B, Jun D) in the rat forebrain after kainic acid-induced limbic seizures. The results demonstrate a complex spatial pattern of IEG induction and/or suppression in limbic and non-limbic structures. The sequence of induction within hippocampal subpopulations was identi cal for all IEGs investigated, following the order dentate gyrus, CA1 and CA3, and irrespective of different temporal profiles for individua l transcription factors. Since Fos and Jun proteins act via homo- and heterodimer complexes at specific DNA sites, our data imply that the p ostictal combinatorial changes of these dimers allow a sequential and differential regulation of target gene expression in specific forebrai n regions. Pretreatment with the non-competitive NMDA receptor antagon ist MK-801 did not affect kainate-induced expression of IEGs in the li mbic system, indicating that IEG induction in these regions is mediate d by high-affinity kainate and AMPA receptors rather than NMDA recepto rs. In contrast, MK-801 abolished IEG induction in the somatosensory c ortex and striatum, suggesting that IEG expression in non-limbic neuro ns occurs transsynaptically and is mediated by NMDA receptors.