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Selective mu- and kappa-opioid receptor antagonists administered into the nucleus accumbens interfere with rapid tolerance to ethanol in rats. Psychopharmacology [Psychopharmacology (Berl)] Journal article

 
TitleSelective mu- and kappa-opioid receptor antagonists administered into the nucleus accumbens interfere with rapid tolerance to ethanol in rats.
Author(s)Varaschin RK, Morato GS 
InstitutionDepartamento de Farmacologia, Centro de Ciências Biológicas, CCB, Universidade Federal de Santa Catarina, Campus Universitário Trindade, 88049-900, Florianópolis, Santa Catarina, Brazil, RVaraschin@salud.unm.edu.
SourcePsychopharmacology (Berl) 2009 Jun 9.
AbstractBACKGROUND: Previous findings have shown that intra-accumbens injection of naltrexone, a non-selective opioid antagonist, blocks the acquisition of rapid tolerance to ethanol in rats. This study investigates the effects of intra-accumbens injection of the selective mu-, delta-, and kappa-opioid antagonists, respectively, naloxonazine, naltrindole, and nor-binaltorphimine, on rapid tolerance to ethanol.
METHODS: Male Wistar rats with guide cannulae directed to the shell or the core portions of the nucleus accumbens received a microinjection of naloxonazine (2-4 mug), naltrindole (2-4 mug), nor-binaltorphimine (2.5-5 mug), or vehicle. After 5 min, each group was divided in two groups that received ethanol (2.7 g/kg i.p.) or saline. Rats were then tested for motor coordination on the tilting plane apparatus. Twenty four hours later, all rats received a challenge dose of ethanol (2.7 g/kg i.p.) and were tested on the tilt plane again.
RESULTS: Repeated injections of ethanol caused a reduction in motor impairment suggesting the development of tolerance. However, rats injected with 4 mug naloxonazine into either core or shell portions of the nucleus accumbens did not exhibit tolerance when challenged with ethanol on day 2. Rats treated with 5 mug nor-binaltorphimine into accumbens core plus intraperitoneal saline on day 1 showed reduced motor impairment when challenged with ethanol on day 2, suggesting cross-tolerance to ethanol.
CONCLUSIONS: Taken together, our results suggests that mu-opioid receptors in both shell and core portions of the nucleus accumbens, and possibly kappa-opioid in the core, participate in the modulation of rapid tolerance to ethanol.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19506836
  
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