Abstract |
The present study was designed to investigate the effects of the mu- opioid morphine, trans-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)- cyclohexyl]- benzene acetamide, methane sulfonate hydrate (U-50488H), a kappa-selective opioid receptor agonist, and 1,3-di-(2-tolyl)guanidine (DTG), sigma-receptor agonist, on the discriminative stimulus properties of cocaine in the rat trained to discriminate 10 mg/kg of cocaine from its vehicle in a shock avoidance paradigm. Morphine (1-5.6 mg/kg), U-50488H (1-10 mg/kg) or 1,3-di-(2-tolyl) guanidine (1 and 10 mg/kg) alone did not produce any stimulus effects in common with cocaine. In contrast, morphine (5.6 mg/kg) and DTG (10 mg/kg), unlike U-50488H (10 mg/kg), significantly shifted the stimulus-generalization curve for cocaine to the left. These results suggest that agonists for mu- opioid- and sigma-receptors augment the discriminative stimulus properties of cocaine.
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Authors | M Ukai, E Mori, T Kameyama |
Journal | Methods and findings in experimental and clinical pharmacology
(Methods Find Exp Clin Pharmacol)
Vol. 19
Issue 8
Pg. 541-6
(Oct 1997)
ISSN: 0379-0355 [Print] Spain |
PMID | 9442477
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Analgesics, Non-Narcotic
- Analgesics, Opioid
- Dopamine Uptake Inhibitors
- Guanidines
- Receptors, Opioid
- 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
- Morphine
- Cocaine
- 1,3-ditolylguanidine
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Topics |
- 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
(pharmacology)
- Analgesics, Non-Narcotic
(pharmacology)
- Analgesics, Opioid
(pharmacology)
- Analysis of Variance
- Animals
- Avoidance Learning
(drug effects)
- Cocaine
(toxicity)
- Discrimination Learning
(drug effects)
- Dopamine Uptake Inhibitors
(toxicity)
- Dose-Response Relationship, Drug
- Guanidines
(pharmacology)
- Male
- Morphine
(pharmacology)
- Rats
- Receptors, Opioid
(agonists)
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