A variety of virus vectors have established that effective gene delivery can be attained in non-dividing mammalian cells. For example, adeno- associated virus (AAV) vectors have been shown to stably transfer and express foreign genes in brain and muscle with little or no accompanying toxicity (McCown et al., 1996; Xiac et al., 1996). Based upon these advances, the present center grant will focus upon the use of AAV and adenovirus (AD) vectors to deliver and express genes proposed to ameliorate the adverse effects of chronic ethanol exposure, both in brain and liver. Therefore, the role of the vector core will be able to construct the cDNA cassettes, insert these cassettes into AAV of Ad vector plasmids, replicate and package the virus vectors, and finally test the function of the vectors, both in vitro and in vivo. Specifically, in Dr. Crews' section, AAV-tyrosine hydroxylase or tryptophan hydroxylase vectors will be prepared to test the involvement of dopaminergic and/or serotonergic function in rodent models of ethanol preference. In Dr. Thurman's section, AAV vectors will be prepared for the delivery of superoxide dismutase (SOD)/catalase, in order to evaluate the origin of ethanol induced oxidative damage to the liver, while Dr. Sulik will use the same AAV vectors to probe the mechanisms of ethanol teratogenicity. For Dr. Brenner, AD vectors will be prepared in order to identify the role of the immediate early genes, APl and NFkappaB, in ethanol-induced ethanol liver pathology. For Dr. Murrow, both sense and antisense AAV vectors will be prepared to delineate the role of GABAa receptor subunits in ethanol self administration, and finally, AAV vectors with antisense constructs to diazepam-binding inhibitor (DBI) and corticotrophan-releasing hormone (CRF) will be prepared for Dr. Breese to probe the role of these factors in the evolution of ethanol withdrawal anxiety. Thus, the vector core will provide the means to investigate molecular mechanisms directly involved in ethanol-induced pathologies, both in the brain and in the liver.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Specialized Center (P50)
Project #
5P50AA011605-03
Application #
6200923
Study Section
Project Start
1999-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
3
Fiscal Year
2000
Total Cost
$178,517
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Jaramillo, Anel A; Randall, Patrick A; Stewart, Spencer et al. (2018) Functional role for cortical-striatal circuitry in modulating alcohol self-administration. Neuropharmacology 130:42-53
Bohnsack, John Peyton; Hughes, Benjamin A; O'Buckley, Todd K et al. (2018) Histone deacetylases mediate GABAA receptor expression, physiology, and behavioral maladaptations in rat models of alcohol dependence. Neuropsychopharmacology 43:1518-1529
Coleman Jr, Leon G; Zou, Jian; Qin, Liya et al. (2018) HMGB1/IL-1? complexes regulate neuroimmune responses in alcoholism. Brain Behav Immun 72:61-77
Coleman Jr, Leon G; Crews, Fulton T (2018) Innate Immune Signaling and Alcohol Use Disorders. Handb Exp Pharmacol 248:369-396
Radke, Anna K; Jury, Nicholas J; Kocharian, Adrina et al. (2017) Chronic EtOH effects on putative measures of compulsive behavior in mice. Addict Biol 22:423-434
Salling, Michael C; Hodge, Christopher J; Psilos, Kelly E et al. (2017) Cue-induced reinstatement of alcohol-seeking behavior is associated with increased CaMKII T286 phosphorylation in the reward pathway of mice. Pharmacol Biochem Behav 163:20-29
Jaramillo, Anel A; Agan, Verda E; Makhijani, Viren H et al. (2017) Functional role for suppression of the insular-striatal circuit in modulating interoceptive effects of alcohol. Addict Biol :
Marshall, S Alex; McKnight, Kyle H; Blose, Allyson K et al. (2017) Modulation of Binge-like Ethanol Consumption by IL-10 Signaling in the Basolateral Amygdala. J Neuroimmune Pharmacol 12:249-259
Lawrimore, Colleen J; Crews, Fulton T (2017) Ethanol, TLR3, and TLR4 Agonists Have Unique Innate Immune Responses in Neuron-Like SH-SY5Y and Microglia-Like BV2. Alcohol Clin Exp Res 41:939-954
Harper, Kathryn M; Knapp, Darin J; Park, Meredith A et al. (2017) Age-related differences in anxiety-like behavior and amygdalar CCL2 responsiveness to stress following alcohol withdrawal in male Wistar rats. Psychopharmacology (Berl) 234:79-88

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