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Operant sensation seeking engages similar neural substrates to operant drug seeking in C57 mice. Neuropsychopharmacology 2009 Jun;34(7):1685-94

Date

01/16/2009

Pubmed ID

19145223

Pubmed Central ID

PMC2720253

DOI

10.1038/npp.2008.226

Scopus ID

2-s2.0-67349231328 (requires institutional sign-in at Scopus site)   94 Citations

Abstract

Novelty and sensation seeking have been associated with elevated drug intake in human and animal studies, suggesting overlap in the circuitry mediating these behaviors. In this study, we found that C57Bl/6J mice readily acquired operant responding for dynamic visual stimuli, a phenomenon we term operant sensation seeking (OSS). Like operant studies using other reinforcers, mice responded on fixed and progressive ratio schedules, were resistant to extinction, and had sustained responding with extended access. We also found that OSS, like psychostimulant self-administration, is sensitive to disruption of dopamine signaling. Low doses of the dopamine antagonist cis-flupenthixol increased active lever responding, an effect reported for psychostimulant self-administration. Additionally, D1-deficient mice failed to acquire OSS, although they readily acquired lever pressing for food. Finally, we found that one common measure of novelty seeking, locomotor activity in a novel open field, did not predict OSS performance. OSS may have predictive validity for screening compounds for use in the treatment of drug addiction. In addition, we also discuss the potential relevance of this animal model to the field of behavioral addictions.

Author List

Olsen CM, Winder DG

Author

Christopher M. Olsen PhD Associate Professor in the Pharmacology and Toxicology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Analysis of Variance
Animals
Behavior, Animal
Conditioning, Operant
Dopamine Antagonists
Exploratory Behavior
Extinction, Psychological
Flupenthixol
Food Preferences
Locomotion
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Photic Stimulation
Receptors, Dopamine D1
Reinforcement Schedule
Self Administration
Signal Transduction