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dc.contributor.authorMarek, Morgan A.
dc.contributor.authorMoe, Simon M.
dc.contributor.authorDe Roach, Elliott
dc.contributor.authorWarner, Jamie
dc.contributor.authorJames, Kimberly F.
dc.contributor.authorAltendorf, Luke R.
dc.contributor.authorPaukner, Dawn
dc.contributor.authorThai, Calvin
dc.contributor.authorHerrmann, Jody
dc.contributor.authorJewett, David C.
dc.contributor.authorRolefson, Kelsey
dc.contributor.authorMoline, Adam D.
dc.contributor.authorEichstadt, Rachel M.
dc.contributor.authorWachholz, Blake
dc.contributor.authorEdwards, Paige A.
dc.contributor.authorVirnig, Austin
dc.date.accessioned2017-03-14T16:16:35Z
dc.date.available2017-03-14T16:16:35Z
dc.date.issued2017-03-14T16:16:35Z
dc.identifier.urihttp://digital.library.wisc.edu/1793/76145
dc.descriptionColor poster with text and graphs.en
dc.description.abstractNaltrexone, an opioid antagonist, is not discriminable at typical doses in operant paradigms. We attempted to establish naltrexone as a discriminative stimulus in rats given 12-hour dark cycle access to sucrose solutions. Interestingly, acute water substitution did not alter the discriminative stimulus effects, suggesting that sucrose consumption produced a long-term change in endorphin function. Chronic (two-week) water substitution eliminated the discriminative stimulus effects of naltrexone. Following chronic water substitution, subjects were again given daily 12-hour dark cycle access to sucrose and 12-hour light cycle access to water for two weeks. Subjects then resumed training, which resulted in rapid reacquisition of the 3.2 mg/kg naltrexone discrimination. Restoring daily sucrose access resulted in all subjects rapidly reacquiring the NTX and saline discrimination. Naltrexone 0.1 mg/kg was discriminable by several subjects. We are currently attempting to train the subjects to reacquire the discrimination of 0.1 mg/kg NTX. Our results suggest that chronic sucrose consumption results in a long term change in endogenous opioid activity.en
dc.description.sponsorshipUniversity of Wisconsin--Eau Claire Office of Research and Sponsored Programsen
dc.language.isoen_USen
dc.relation.ispartofseriesUSGZE AS589;
dc.subjectPostersen
dc.subjectNaltrexoneen
dc.subjectDiscrimination learningen
dc.subjectRatsen
dc.titleDiscriminative stimulus effects of naltrexone in rats with limited access to sucroseen
dc.typePresentationen


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