Investigating the role of extrasynaptic GABAA receptors located in the infralimbic cortex in the binge-like alcohol intake of male C57BL/6J mice

dc.contributor.advisorBoehm, Stephen
dc.contributor.authorFritz, Brandon Michael
dc.contributor.otherCzachowsk, Cristine
dc.contributor.otherGrahame, Nicholas J.
dc.date.accessioned2013-11-20T14:55:35Z
dc.date.available2013-11-20T14:55:35Z
dc.date.issued2013-11-20
dc.degree.date2013en_US
dc.degree.disciplineDepartment of Psychologyen
dc.degree.grantorPurdue Universityen_US
dc.degree.levelM.S.en_US
dc.descriptionIndiana University-Purdue University Indianapolis (IUPUI)en_US
dc.description.abstractExtrasynaptic GABAA receptors, often identified as those containing both α4 and δ subunits, appear to be a target for the actions of alcohol (ethanol) at relatively low concentrations, perhaps suppressing the activity of GABAergic interneurons which regulate activity in the mesolimbocortical circuit. Pharmacological studies in rodents using the δ-subunit selective agonist Gaboxadol (THIP) have found both promotional and inhibitory effects on alcohol consumption. The goal of this project was to determine the role of extrasynaptic GABAA receptors located in the infralimbic cortex (ILC) in the binge-like alcohol intake of male C57BL/6J (B6) mice. The ILC is of interest due to its demonstrated involvement in stress reactivity and alcohol exposure has been shown to interfere with extinction learning; impairments of which may be related to inflexible behavior (i.e. problematic alcohol consumption). Adult male B6 mice were bilaterally implanted with stainless steel guide cannulae aimed at the ILC and were offered limited access to 20% ethanol or 5% sucrose for 6 days. On day 7, mice were bilaterally injected with 50 or 100 ng THIP (25 or 50 ng per side respectively) or saline vehicle into the ILC. It was found that the highest dose of THIP (100 ng/mouse) increased alcohol intake relative to vehicle controls, although control animals consumed relatively little ethanol following infusion. Furthermore, THIP had no effect on sucrose consumption (p > 0.05), suggesting that the effect of THIP was selective for ethanol consumption. Together, these findings suggest that the mice that consumed ethanol may have been particularly reactive to the microinfusion process relative to animals that consumed sucrose, perhaps because ethanol consumption was not as reinforcing as sucrose consumption. In addition, the observation that THIP effectively prevented the decrease in ethanol intake on day 7 induced by the microinjection process may be related to a role for the ILC in adaptive learning processes, which in turn, promote behavioral flexibility.en_US
dc.identifier.urihttps://hdl.handle.net/1805/3694
dc.identifier.urihttp://dx.doi.org/10.7912/C2/1067
dc.language.isoen_USen_US
dc.subjectMouseen_US
dc.subjectAlcoholen_US
dc.subjectGABAen_US
dc.subjectBinge Drinkingen_US
dc.subjectInfralimbic Cortexen_US
dc.subject.lcshBinge drinking -- Researchen_US
dc.subject.lcshAlcohol -- Pathophysiologyen_US
dc.subject.lcshAlcoholism -- Researchen_US
dc.subject.lcshPrefrontal cortexen_US
dc.subject.lcshMice as laboratory animalsen_US
dc.subject.lcshMice -- Physiologyen_US
dc.subject.lcshEthanol -- Researchen_US
dc.subject.lcshNeuropsychopharmacologyen_US
dc.subject.lcshGABA -- Receptorsen_US
dc.subject.lcshReinforcement (Psychology) -- Researchen_US
dc.subject.lcshStress (Psychology)en_US
dc.subject.lcshStress (Physiology)en_US
dc.titleInvestigating the role of extrasynaptic GABAA receptors located in the infralimbic cortex in the binge-like alcohol intake of male C57BL/6J miceen_US
dc.typethesisen
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