http://www.cnr.it/ontology/cnr/individuo/prodotto/ID37558
Functional interaction between opioid and cannabinoid receptors in drug self-administration. (Articolo in rivista)
- Type
- Label
- Functional interaction between opioid and cannabinoid receptors in drug self-administration. (Articolo in rivista) (literal)
- Anno
- 2001-01-01T00:00:00+01:00 (literal)
- Alternative label
Navarro M, 1 Carrera MR, 2 Fratta W, 1 Valverde O, 2 Cossu G, 3 Fattore L, 1 Chowen JA, 2 Gomez R, 1 del Arco I, 1 Villanua MA, 1 Maldonado R, 4 Koob GF, 1 Rodriguez de Fonseca F. (2001)
Functional interaction between opioid and cannabinoid receptors in drug self-administration.
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Navarro M, 1 Carrera MR, 2 Fratta W, 1 Valverde O, 2 Cossu G, 3 Fattore L, 1 Chowen JA, 2 Gomez R, 1 del Arco I, 1 Villanua MA, 1 Maldonado R, 4 Koob GF, 1 Rodriguez de Fonseca F. (literal)
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- ISI Web of Science (WOS) (literal)
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- 1 Uni Madrid
2 Uni Cagliari
3 CNR
4 La Jolla, California (USA) (literal)
- Titolo
- Functional interaction between opioid and cannabinoid receptors in drug self-administration. (literal)
- Abstract
- The present study was designed to explore the relationship between the cannabinoid and opioid receptors in animal models of opioid-induced reinforcement. The acute administration of SR141716A, a selective central cannabinoid CB1 receptor antagonist, blocked heroin self-administration in rats, as well as morphine-induced place preference and morphine self-administration in mice. Morphine-dependent animals injected with SR141716A exhibited a partial opiate-like withdrawal syndrome that had limited consequences on operant responses for food and induced place aversion. These effects were associated with morphine-induced changes in the expression of CB1 receptor mRNA in specific nuclei of the reward circuit, including dorsal caudate putamen, nucleus accumbens, and septum. Additionally, the opioid antagonist naloxone precipitated a mild cannabinoid-like withdrawal syndrome in cannabinoid-dependent rats and blocked cannabinoid self-administration in mice. Neither SR141716A nor naloxone produced any intrinsic effect on these behavioral models. The present results show the existence of a cross-interaction between opioid and cannabinoid systems in behavioral responses related to addiction and open new strategies for the treatment of opiate dependence.
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