
pmid: 17196636
There is evidence that the neuropeptide cholecystokinin (CCK) is important for the rewarding effects of drugs of abuse. However, less is known regarding the role of CCK in drug seeking and craving. The present study investigated whether the CCK(B) antagonist L-365, 260 could block morphine-induced drug seeking using the conditioned place preference paradigm and whether the dopaminergic reward pathway contributes to the effect of L-365, 260 on expression of morphine place preference. We found that systemic administration of the CCK(B) antagonist L-365, 260 attenuates the expression of morphine-induced drug seeking as assessed using conditioned place preference (CPP) and shows that this effect is mediated by CCK(B) receptors in the anterior nucleus accumbens (NAcc). Additionally, we demonstrate that this effect is dependent on D(2) receptor activation in the anterior nucleus accumbens (NAcc). These results indicate that endogenous CCK modulates the incentive-salience of morphine-associated cues and suggest that CCK antagonists may be useful in the treatment of drug craving.
Male, Benzodiazepinones, Morphine, Receptors, Dopamine D2, Phenylurea Compounds, Nucleus Accumbens, Receptor, Cholecystokinin B, Rats, Rats, Sprague-Dawley, Animals, Conditioning, Operant, Cholecystokinin, Morphine Dependence
Male, Benzodiazepinones, Morphine, Receptors, Dopamine D2, Phenylurea Compounds, Nucleus Accumbens, Receptor, Cholecystokinin B, Rats, Rats, Sprague-Dawley, Animals, Conditioning, Operant, Cholecystokinin, Morphine Dependence
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