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Publication : ΔFosB enhances the rewarding effects of cocaine while reducing the pro-depressive effects of the kappa-opioid receptor agonist U50488.

First Author  Muschamp JW Year  2012
Journal  Biol Psychiatry Volume  71
Issue  1 Pages  44-50
PubMed ID  21962331 Mgi Jnum  J:283294
Mgi Id  MGI:6386076 Doi  10.1016/j.biopsych.2011.08.011
Citation  Muschamp JW, et al. (2012) DeltaFosB enhances the rewarding effects of cocaine while reducing the pro-depressive effects of the kappa-opioid receptor agonist U50488. Biol Psychiatry 71(1):44-50
abstractText  BACKGROUND: Elevated expression of the transcription factor DeltaFosB accompanies repeated exposure to drugs of abuse, particularly in brain areas associated with reward and motivation (e.g., nucleus accumbens). The persistent effects of DeltaFosB on target genes might play an important role in the development and expression of behavioral adaptations that characterize addiction. This study examines how DeltaFosB influences the responsiveness of the brain reward system to rewarding and aversive drugs. METHODS: We used the intracranial self-stimulation paradigm to assess the effects of cocaine in transgenic mice with inducible overexpression of DeltaFosB in striatal regions (including nucleus accumbens and dorsal striatum). Mice implanted with lateral hypothalamic stimulating electrodes were trained with the "rate-frequency" procedure for intracranial self-stimulation to determine the frequency at which stimulation becomes rewarding (threshold). RESULTS: A dose-effect analysis of cocaine effects revealed that mice overexpressing DeltaFosB show increased sensitivity to the rewarding (threshold-lowering) effects of the drug, compared with littermate control subjects. Interestingly, mice overexpressing DeltaFosB were also less sensitive to the pro-depressive (threshold-elevating) effects of U50488, a kappa-opioid agonist known to induce dysphoria and stress-like effects in rodents. CONCLUSIONS: These data suggest that induction of DeltaFosB in striatal regions has two important behavioral consequences-increased sensitivity to drug reward, and reduced sensitivity to aversion-producing a complex phenotype that shows signs of vulnerability to addiction as well as resilience to stress.
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