The Animal and Behavior Core will provide services, technical assistance and training needed for thebreeding and behavioral testing of the knockout and knock-in mice that will be examined by the investigatorswithin the research components. Centralized breeding and genotyping will maximize efficiency and allow forthe development and use of a centralized system for tracking the production and use of all mice createdunder this center. In addition, the Animal and Behavior Core will standardize the methods and the analysesfor alcohol-related behavioral testing for mice and rats. A series of behavioral tests will evaluate the acutesedating and ataxic effects of alcohol, as well as the reinforcing and rewarding properties of alcohol, in micegenerated by the research components. The Core will instruct research personnel in the conduct of otherbehavioral studies, as needed. By conducting the bulk of the behavioral testing within the Core, we ensurethat the procedures are performed, and the data are analyzed, in a consistent manner, allowing for maximalcomparability of the effects of different genetic manipulations across center projects. The Core willadditionally seek to develop a useful and reliable protocol for operant self-administration of alcohol by micethat produces a maximal level of alcohol intake for future use by the research components.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Specialized Center (P50)
Project #
1P50AA017072-01
Application #
7497320
Study Section
Special Emphasis Panel (ZAA1-BB (11))
Project Start
2008-05-20
Project End
2013-04-30
Budget Start
2008-05-20
Budget End
2009-04-30
Support Year
1
Fiscal Year
2008
Total Cost
$704,444
Indirect Cost
Name
Ernest Gallo Clinic and Research Center
Department
Type
DUNS #
173995366
City
Emeryville
State
CA
Country
United States
Zip Code
94608
Barak, Segev; Ahmadiantehrani, Somayeh; Logrip, Marian L et al. (2018) GDNF and alcohol use disorder. Addict Biol :
Ron, Dorit; Berger, Anthony (2018) Targeting the intracellular signaling ""STOP"" and ""GO"" pathways for the treatment of alcohol use disorders. Psychopharmacology (Berl) 235:1727-1743
Blegen, Mariah B; da Silva E Silva, Daniel; Bock, Roland et al. (2018) Alcohol operant self-administration: Investigating how alcohol-seeking behaviors predict drinking in mice using two operant approaches. Alcohol 67:23-36
Vandenberg, Angela; Lin, Wan Chen; Tai, Lung-Hao et al. (2018) Mice engineered to mimic a common Val66Met polymorphism in the BDNF gene show greater sensitivity to reversal in environmental contingencies. Dev Cogn Neurosci 34:34-41
Saunders, Benjamin T; Richard, Jocelyn M; Margolis, Elyssa B et al. (2018) Dopamine neurons create Pavlovian conditioned stimuli with circuit-defined motivational properties. Nat Neurosci 21:1072-1083
Laguesse, Sophie; Morisot, Nadege; Phamluong, Khanhky et al. (2018) mTORC2 in the dorsomedial striatum of mice contributes to alcohol-dependent F-Actin polymerization, structural modifications, and consumption. Neuropsychopharmacology 43:1539-1547
Bird, C W; Baculis, B C; Mayfield, J J et al. (2018) The brain-derived neurotrophic factor VAL68MET polymorphism modulates how developmental ethanol exposure impacts the hippocampus. Genes Brain Behav :e12484
Blasio, Angelo; Wang, Jingyi; Wang, Dan et al. (2018) Novel Small-Molecule Inhibitors of Protein Kinase C Epsilon Reduce Ethanol Consumption in Mice. Biol Psychiatry 84:193-201
Fan, Qi Wen; Nicolaides, Theodore P; Weiss, William A (2018) Inhibiting 4EBP1 in Glioblastoma. Clin Cancer Res 24:14-21
Wegner, Scott A; Pollard, Katherine A; Kharazia, Viktor et al. (2017) Limited Excessive Voluntary Alcohol Drinking Leads to Liver Dysfunction in Mice. Alcohol Clin Exp Res 41:345-358

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