An array of evidence indicates that long-term exposure to cocaine alters several components of the brain dopamine system. Because the release of dopamine in the nucleus accumbens (NAc) has been implicated in mediating the reinforcing effects of cocaine, changes in dopamine function can have profound
Effect of cocaine self-administration on dopamine D2 receptors in rhesus monkeys
โ Scribed by Rodney J. Moore; Sharon L. Vinsant; Michael A. Nader; Linda J. Porrino; David P. Friedman
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 279 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0887-4476
No coin nor oath required. For personal study only.
โฆ Synopsis
The present study used autoradiography to examine the effects of chronic self-administration of cocaine on the density of dopamine D 2 receptors in nonhuman primates. Three rhesus monkeys intravenously self-administered an average of 1.35 mg/kg cocaine per day for 18-22 months until they were euthanized immediately after a self-administration session. Binding site density of the D 2 ligand [ 3 H]raclopride (2 nM) was assessed in these monkeys as well as three untreated controls, using quantitative in vitro receptor autoradiography. As compared to untreated controls, D 2 binding site density was significantly lower in the animals that self-administered cocaine in all regions of the striatum rostral to the anterior commissure. These regions include the anterior and central regions of the caudate nucleus, putamen, olfactory tubercle, and both the shell and core of the nucleus accumbens. Within the substantia nigra and ventral tegmental area, by contrast, no differences were found in the density of D 2 binding sites. These findings suggest a pervasive effect of cocaine on the regulation of D 2 receptors in the striatum. The lack of change within the ventral midbrain, however, suggests a differential regulation of D 2 receptors in the striatum and ventral midbrain. This study confirms and extends our knowledge of the neurobiological changes in the mesolimbic dopamine system that result from chronic exposure to cocaine.
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