The overall goal of this proposal is to provide mentored career development for a young scientist. The training and research support detailed in this proposal will enable the Candidate to utilize a multidisciplinary approach to understand factors that modulate the stimulus properties of ethanol. Importantly, this training will contribute to her development as an independent investigator. The Candidate will receive broad-based training in alcoholism research as well as several methods that will be required to address the research plan including immunohistochemistry techniques, confocal microscopy, stereotaxic surgeries and microinjection of drugs. The research plan will focus on the role of metabotropic glutamate receptors (mGluRs) in ethanol's discriminative stimulus effects. mGluRs have been shown to influence GABAA and glutamate functioning which are major components of ethanol's stimulus properties. The Candidate will test the hypothesis that mGluRS and mGluR2/3 can modulate ethanol discrimination by interaction with GABAA and NMDA receptor systems.
Specific Aim 1 will utilize behavioral pharmacology techniques to determine if an antagonist of mGluRS and an agonist of mGluR2/3 will modulate ethanol discrimination, and the ethanol-like stimulus properties of GABAA positive modulators and NMDA antagonists.
Specific Aim 2 will use dual-label immunohistochemistry with confocal visualization to evaluate if mGluRS and mGluR2/3 are co-expressed with GABAA and NMDA receptor subunits in ethanol discrimination trained rats.
Specific Aim 3 will use immunohistochemisty techniques (Fos-like immunoreactivity) to assess brain regional involvement in ethanol discrimination and in mGluRS and mGluR2/3 modulation of ethanol discrimination and ethanol substitutes (diazepam and MK-801).
Specific Aim 4 will use microinjection techniques to assess ethanol discrimination and the substitution of diazepam and MK-801 after administration of the mGluRS antagonist and the mGluR2/3 agonist into specific brain regions that show high levels of mGluR co-expression with GABAA and NMDA receptors as determined from Aim 2 and show anatomical involvement as determined from Aim 3. We predict that these experiments will reveal a modulatory role of mGluRS and mGluR2/3 in ethanol discrimination. Further, incorporating these techniques is highly innovative, and these studies will generate novel findings regarding the involvement of mGluRS and mGluR2/3 in the stimulus properties of ethanol. Understanding these mechanisms is important to basic science and has numerous implications for development of therapeutic interventions in alcoholism, especially given that the discriminative stimulus properties of drugs can be important determinants of abuse liability.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
1K01AA016009-01
Application #
7027586
Study Section
Health Services Research Review Subcommittee (AA)
Program Officer
Egli, Mark
Project Start
2006-06-01
Project End
2011-05-31
Budget Start
2006-06-01
Budget End
2007-05-31
Support Year
1
Fiscal Year
2006
Total Cost
$104,910
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Psychology
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Besheer, Joyce; Fisher, Kristen R; Lindsay, Tessa G et al. (2013) Transient increase in alcohol self-administration following a period of chronic exposure to corticosterone. Neuropharmacology 72:139-47
Besheer, Joyce; Fisher, Kristen R; Cannady, Reginald et al. (2012) Intra-amygdala inhibition of ERK(1/2) potentiates the discriminative stimulus effects of alcohol. Behav Brain Res 228:398-405
Besheer, Joyce; Fisher, Kristen R; Grondin, Julie J M et al. (2012) The effects of repeated corticosterone exposure on the interoceptive effects of alcohol in rats. Psychopharmacology (Berl) 220:809-22
Besheer, Joyce; Fisher, Kristen R; Durant, Brandon (2012) Assessment of the interoceptive effects of alcohol in rats using short-term training procedures. Alcohol 46:747-55
Cannady, Reginald; Grondin, Julie J M; Fisher, Kristen R et al. (2011) Activation of group II metabotropic glutamate receptors inhibits the discriminative stimulus effects of alcohol via selective activity within the amygdala. Neuropsychopharmacology 36:2328-38
Besheer, Joyce; Grondin, Julie J M; Cannady, Reginald et al. (2010) Metabotropic glutamate receptor 5 activity in the nucleus accumbens is required for the maintenance of ethanol self-administration in a rat genetic model of high alcohol intake. Biol Psychiatry 67:812-22
Besheer, Joyce; Lindsay, Tessa G; O'Buckley, Todd K et al. (2010) Pregnenolone and ganaxolone reduce operant ethanol self-administration in alcohol-preferring p rats. Alcohol Clin Exp Res 34:2044-52
Besheer, Joyce; Grondin, Julie J M; Salling, Michael C et al. (2009) Interoceptive effects of alcohol require mGlu5 receptor activity in the nucleus accumbens. J Neurosci 29:9582-91
Besheer, Joyce; Schroeder, Jason P; Stevenson, Rebekah A et al. (2008) Ethanol-induced alterations of c-Fos immunoreactivity in specific limbic brain regions following ethanol discrimination training. Brain Res 1232:124-31
Besheer, Joyce; Faccidomo, Sara; Grondin, Julie J M et al. (2008) Regulation of motivation to self-administer ethanol by mGluR5 in alcohol-preferring (P) rats. Alcohol Clin Exp Res 32:209-21

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