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Differential development of behavioral tolerance and the subsequent hedonic effects of alcohol in AA and ANA rats

dc.contributor.authorGauvin, David V.en_US
dc.contributor.authorBriscoe, Richard J.en_US
dc.contributor.authorBaird, Theodore J.en_US
dc.date.accessioned2006-09-08T19:50:12Z
dc.date.available2006-09-08T19:50:12Z
dc.date.issued2000-09en_US
dc.identifier.citationGauvin, David V.; Baird, Theodore J.; Briscoe, Richard J.; (2000). "Differential development of behavioral tolerance and the subsequent hedonic effects of alcohol in AA and ANA rats." Psychopharmacology 151(4): 335-343. <http://hdl.handle.net/2027.42/41974>en_US
dc.identifier.issn0033-3158en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41974
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11026740&dopt=citationen_US
dc.description.abstractRationale: There at least two ways in which tolerance development to alcohol's behavioral effects could interact with its subsequent intake: 1) tolerance to alcohol's reward or reinforcing effects per se could lead to increased consumption, and 2) tolerance to alcohol's aversive effects could unmask alcohol's rewarding effects. These two mechanisms may differentially interact with preexisting genetic traits underlying alcoholism. Objectives: Alcohol's subjective attributes were assessed in selectively bred AA and ANA rats after the development of tolerance to alcohol's behaviorally disruptive effects on lever-press performance. Methods: Rats were trained to press a lever under an FR30 schedule of food presentations. Group-dependent differential access to intoxicated practice, using a typical pre-post drug administration design, was utilized to promote the development of alcohol tolerance in only the group receiving intoxicated practice sessions. Subsequently, rats were trained to associate alcohol with unique place and taste stimuli in order to assess the relative changes in the approach towards, or avoidance of alcohol-related cues in each group. Results: Groups of AA and ANA rats given access to intoxicated practice demonstrated tolerance development. These groups subsequently conditioned place preferences and failed to develop conditioned taste aversions to alcohol. Passive alcohol exposure in the ANA rats set the occasion for the development of a place preference and delayed taste conditioning. AA rats exposed to passive alcohol exposure failed to condition place preferences and developed rapid taste aversions. Saline control rats failed to develop tolerance or place preferences but did condition a robust alcohol-induced taste aversion. Conclusions: AA and ANA rats differ in their behavioral and pharmacokinetic response to chronic alcohol exposure. Compensatory responses interacting with approach-avoidance behaviors appear to be learned during intoxicated practice in the AA rats and during both intoxicated practice and passive exposure in the ANA rat line.en_US
dc.format.extent144856 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherLegacyen_US
dc.subject.otherAA and ANA Rats Associative Learning Conditioned Place Preference Conditioned Taste Aversion Behavioral Tolerance Alcoholen_US
dc.titleDifferential development of behavioral tolerance and the subsequent hedonic effects of alcohol in AA and ANA ratsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pharmacology, 1301 MSRB III, University of Michigan School of Medicine, 1150 W. Medical Center Drive, Ann Arbor, MI 48109-0632, USA,en_US
dc.contributor.affiliationotherMPI Research, 54943 N. Main St., Mattawan, MI 49071, USA,en_US
dc.contributor.affiliationotherDrug and Chemical Evaluation Section, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, USA,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid11026740en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41974/1/213-151-4-335_s002130000477.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s002130000477en_US
dc.identifier.sourcePsychopharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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