Korean J Physiol Pharmacol.
2001 Aug;5(4):299-305.
Regulation of phosphorylated cAMP response element-binding protein, Fos-related antigen and FosB expression by dopamine agonists in rat striatum
- Affiliations
-
- 1Department of Physiology, Yeungnam University College of Medicine, Daegu, South Korea. jykim@med.yu.ac.kr
Abstract
- Activation of D1-like dopamine receptors by psychostimulants,
such as amphetamine, upregulates the expression of immediate early gene
and opioid peptide gene in the striatum. The genomic changes are
regulated by phosphorylated transcription factors via complicated
intracellular events. To evaluate temporal expression of the
transcription factors by dopaminergic stimulation, the D1-like dopamine
agonist, amphetamine or SKF82958, was systematically delivered. As
intracellular markers in response to the agonist, phosphorylated cAMP
response element-binding protein (pCREB), Fos-related antigens (FRA) and
FosB immunoreactivity (IR) was compared at 20 and 120 min time points in
the selected areas of the striatum. Semi-quantitative immunocytochemistry
showed that amphetamine (5 mg/kg, i.p.) significantly increased pCREB-IR
at 20 min, sustained up to 60 min and decreased at 120 min after the
infusion. Like amphetamine, the full D1 agonist, SKF82958 (0.5 mg/kg,
s.c.), also increased pCREB-IR at 20 min, but not at 120 min after the
infusion in the dorsal striatum (caudoputaman, CPu) and shell of ventral
striatum (nucleus accumbens, NAc). In contrast, FRA- and FosB-IR induced
by SKF82958 was significantly increased at 120 min, but not at 20 min
after the administration. These data indicate that SKF82958 mimics
induction of CREB phosphorylation by amphetamine and differentially
regulates temporal induction of pCREB, and FRA and FosB expression in the
striatum.