MORPHINE INDUCES C-FOS AND JUNB IN STRIATUM AND NUCLEUS-ACCUMBENS VIAD-1 AND N-METHYL-D-ASPARTATE RECEPTORS

Citation
Jl. Liu et al., MORPHINE INDUCES C-FOS AND JUNB IN STRIATUM AND NUCLEUS-ACCUMBENS VIAD-1 AND N-METHYL-D-ASPARTATE RECEPTORS, Proceedings of the National Academy of Sciences of the United Statesof America, 91(18), 1994, pp. 8537-8541
Citations number
80
Categorie Soggetti
Multidisciplinary Sciences
ISSN journal
00278424
Volume
91
Issue
18
Year of publication
1994
Pages
8537 - 8541
Database
ISI
SICI code
0027-8424(1994)91:18<8537:MICAJI>2.0.ZU;2-Y
Abstract
Morphine induced the c-fos and junB immediate early genes in neurons o f the medial and ventral striatum and nucleus accumbens. Induction of c-fos and junB mRNA and Fos protein was blocked by naloxone, the D-1 d opamine (DA) receptor antagonists SCH23390 and SCH39166, and the N-met hyl-D-aspartate (NMDA) glutamate receptor antagonist MK801. SCH23390 a ttenuated morphine induction of AP-1 binding in striatum, suggesting t hat c-fos and junB contribute to AP-1 binding. SCH23390 and MK801 did not block morphine induction of c-fos and junB in septum. Since the mo rphine induction of c-fos and junB in striatum and nucleus accumbens ( NA) was similar to that observed with cocaine and amphetamine, these d ata support current concepts that limbic striatum and NA are among the brain regions that mediate drug abuse. Furthermore, since DA and NMDA receptors may mediate opiate reward and opiate induction of c-fos and junB, the DA/NMDA regulation of c-fos and junB and their target genes may produce long-term changes in the striatal and NA circuits that co ntribute to opiate drug abuse.