ISSN:
1432-2072
Keywords:
Cocaine
;
Quinpirole
;
SKF 38393
;
D1 agonist
;
D2 agonist
;
Drug interactions
;
Route of administration
;
Discriminative-stimulus effects
;
Behavior
;
Squirrel monkeys
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstract The present study was designed to assess the behavioral similarity of the effects of prototype dopamine receptor-subtype selective agonists and cocaine. Squirrel monkeys (N=4) were trained with food reinforcement to press one of two levers after administration of IV cocaine (0.3 mg/kg) or the other lever after saline. After training, IV cocaine produced reliable responding on the cocaine lever (〉98%), whereas saline produced reliable responding on the alternate lever (〉98%). The D2 agonist, quinpirole (0.003–1.0 mg/kg, IM), produced dose-related increases in cocaine-appropriate responding, with maximal effects of 62%. When delivered IV, quinpirole (0.01–0.17 mg/kg) was approximately twice as potent, but no more effective. The D1 agonist, SKF 38393 (0.3–30.0 mg/kg, IM or 3.0–17.0 mg/kg, IV) failed to produce any significant cocaine-appropriate responding. Further, pretreatment with SKF 38393 (either 0.3 or 10.0 mg/kg, IM) did not significantly alter the the quinpirole (0.01–1.0 mg/kg, IM) dose-effect curve. The effects of these drugs differ from those previously reported in rats, suggesting a species difference that may be of importance in evaluating the behavioral pharmacology of cocaine.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF02245140
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