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dc.contributor.authorPanlilio, LV
dc.contributor.authorHogarth, L
dc.contributor.authorShoaib, M
dc.date.accessioned2016-02-29T14:14:26Z
dc.date.issued2014-11-01
dc.description.abstractBACKGROUND: Animal models that allow concurrent access to drug and nondrug reinforcers provide unique insight into the etiology, maintenance, and treatment of drug use. OBJECTIVES: We sought to develop and utilize a concurrent access procedure with nicotine and sucrose in rats. METHODS: Pressing one lever delivered intravenous nicotine, and pressing another lever delivered sucrose pellets, with both reinforcers freely available throughout daily sessions. RESULTS: Rats that had been pretrained with nicotine on some days and sucrose on other days responded on both levers when subsequently given concurrent access, but almost all responded at substantially higher rates on the sucrose lever. In contrast, rats pretrained exclusively with nicotine before being given concurrent access showed individual differences, with about half responding more on the nicotine lever. Treatment with the nicotinic receptor partial agonist varenicline selectively decreased nicotine self-administration. Food restriction and removal of the sucrose lever both increased nicotine self-administration. CONCLUSIONS: The finding that rats continue to take nicotine when sucrose is concurrently available-and in many cases take it more frequently than sucrose-demonstrates that nicotine self-administration does not only occur in the absence of alternative reinforcement options. As a model of human nicotine use, concurrent access is more naturalistic and has higher face validity than procedures in which only one reinforcer is available or choosing one reinforcer precludes access to other reinforcers. As such, this procedure could be useful for evaluating therapeutic agents and improving our understanding of environmental conditions that promote or discourage nicotine use.en_GB
dc.description.sponsorshipAll experiments were conducted at Newcastle University and supported by internal funds from Newcastle University and funds donated by Dr. L. Hogarth (MRC G0701456). Preparation of the manuscript was supported by the Intramural Research Program of the National Institute on Drug Abuse, National Institutes of Health, Department of Health and Human Services (LVP).en_GB
dc.identifier.citationApril 2015, Vol. 232, Iss. 8, pp. 1451 - 1460en_GB
dc.identifier.doi10.1007/s00213-014-3787-8
dc.identifier.urihttp://hdl.handle.net/10871/20257
dc.language.isoenen_GB
dc.publisherSpringer Verlag (Germany)en_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/25366874en_GB
dc.relation.urlhttp://link.springer.com/article/10.1007%2Fs00213-014-3787-8en_GB
dc.rightsThis is the author accepted manuscript. The final version is available from Springer Verlag via http://dx.doi.org/10.1007/s00213-014-3787-8.en_GB
dc.subjectAnimalsen_GB
dc.subjectBehavior, Addictiveen_GB
dc.subjectBenzazepinesen_GB
dc.subjectConditioning, Operanten_GB
dc.subjectMaleen_GB
dc.subjectNicotineen_GB
dc.subjectQuinoxalinesen_GB
dc.subjectRatsen_GB
dc.subjectRats, Sprague-Dawleyen_GB
dc.subjectReinforcement (Psychology)en_GB
dc.subjectSelf Administrationen_GB
dc.subjectSucroseen_GB
dc.subjectVareniclineen_GB
dc.titleConcurrent access to nicotine and sucrose in rats.en_GB
dc.typeArticleen_GB
dc.date.available2016-02-29T14:14:26Z
dc.identifier.issn0033-3158
exeter.place-of-publicationGermany
dc.descriptionPublisheden_GB
dc.descriptionJournal Articleen_GB
dc.descriptionResearch Support, N.I.H., Intramuralen_GB
dc.descriptionResearch Support, Non-U.S. Gov'ten_GB
dc.identifier.eissn1432-2072
dc.identifier.journalPsychopharmacologyen_GB


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