In vivo NMDA/dopamine interaction resulting in Fos production in the limbic system and basal ganglia of the mouse brain

Citation
J. Radulovic et al., In vivo NMDA/dopamine interaction resulting in Fos production in the limbic system and basal ganglia of the mouse brain, MOL BRAIN R, 75(2), 2000, pp. 271-280
Citations number
61
Categorie Soggetti
Neurosciences & Behavoir
Journal title
MOLECULAR BRAIN RESEARCH
ISSN journal
0169328X → ACNP
Volume
75
Issue
2
Year of publication
2000
Pages
271 - 280
Database
ISI
SICI code
0169-328X(20000222)75:2<271:IVNIRI>2.0.ZU;2-V
Abstract
Glutamatergic and dopaminergic Glutamatergic and dopaminergic effects on mo lecular processes have been extensively investigated in the basal ganglia. It has been demonstrated that NMDA and dopamine D-1 and D-2 receptors inter act in the regulation of signal transduction and induction of transcription factors. In the present experiments, NMDA/dopamine interactions were inves tigated in the normosensitive caudate nucleus, hippocampus and amygdala by monitoring Fos production. We demonstrated that NMDA and the D-1 receptor a gonist SKF 38393 triggered Fos levels in a distinct, non-overlapping and re gion-specific pattern. NMDA injected intraperitoneally (i.p.) elevated Fos levels in all hippocampal subfields and the central amygdala, whereas SKF 3 8393 triggered Fos production in basomedial, cortical, medial amygdala and caudate nucleus. The NMDA receptor antagonist CGS 19755 prevented NMDA- and SKF 38393-triggered Fos production in all investigated brain areas. Simila rly, the D-1 receptor antagonist SCH 23390 inhibited the effects produced b y SKF 38393 or NMDA. The D-2 receptor antagonist sulpiride exerted synergis tic and antagonistic effects on NMDA- and SKF 38393-triggered Fos productio n, in a region specific manner. These data suggest that NMDA and dopamine r eceptors regulate Fos production within I-he limbic system and basal,gangli a through regionally differentiated but interdependent actions. (C) 2000 El sevier Science B.V. All rights reserved.