The effects of D-1 or D-2 dopamine receptor blockade on zif/268 and preprodynorphin gene expression in rat forebrain following a short-term cocaine binge

被引:46
作者
Daunais, JB [1 ]
McGinty, JF [1 ]
机构
[1] E CAROLINA UNIV, SCH MED, DEPT ANAT & CELL BIOL, GREENVILLE, NC 27858 USA
来源
MOLECULAR BRAIN RESEARCH | 1996年 / 35卷 / 1-2期
关键词
SCH; 23390; sulpiride; opioid; in situ hybridization; striatum; sensorimotor cortex; psychostimulant; immediate early gene; transcription factors;
D O I
10.1016/0169-328X(95)00226-I
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Selective D-1 or D-2 dopamine receptor antagonists were used to investigate the transynaptic regulation of mRNAs coding for the opioid peptide, preprodynorphin, and the nuclear transcription factor, zif/268 after an acute cocaine binge. Rats were injected intraperitoneally with the D-1 receptor antagonist, SCH 23390, or the D-2 receptor antagonist, sulpiride, 30 min prior to 3 hourly injections of saline or 20 mg/kg cocaine and killed 1 h after the final injection. Behavioral ratings indicated that SCH 23390 blocked, whereas sulpiride augmented, cocaine-induced stereotypical behaviors. Striatal sections were hybridized with oligonucleotides coding for zif/268 and preprodynorphin. Quantitative image analysis of autoradiograms revealed that (1) SCH 23390 completely suppressed basal and cocaine binge-induced zif/268 mRNA in the striatal and cerebral cortical areas examined; (2) sulpiride enhanced basal levels of zif/268 mRNA in the medial caudate and dorsomedial shell of the nucleus accumbens; (3) sulpiride partially blocked cocaine binge-induced levels of zif/268 mRNA in the dorsal striatum but had no effect in sensory cortex; (4) SCH 23390, but not sulpiride, significantly reduced the constitutive expression of preprodynorphin mRNA; and (5) SCH 23390 and sulpiride blocked cocaine binge-induced expression of preprodynorphin mRNA in the dorsal striatum.
引用
收藏
页码:237 / 248
页数:12
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