The purpose of the Animal Core Component is to maintain and produce selectively bred lines and strains of mice for use by ARC investigators. Virtually all of these strain and lines of mice have been developed by the ARC as animal models for studying CNS mechanisms that mediate specific actions of ethanol and for identifying genes that mediate differences in ethanol sensitivity and acute tolerance. Maintenance and production of all mice are performed in the specific pathogen-free facilities of the Institute for Behavioral Genetics (IBG) located in Boulder, as needed, the animals are delivered from IBG to ARC investigators at UCHSC in Denver. Inbred strains of mice to be produced include the ILS, ISS, and the LS X SS Recombinant inbred strains that were derived from the LS and SS lines (selectively bred for differences in hypnotic sensitivity to ethanol). These strains and F2 generations derived from them are uniquely valuable for discovering genes that regulate hypnotic sensitivity to ethanol and for determining the behavioral, electrophysiological, and neurochemical effects attributable to polymorphisms in those genes. Another animal population that is invaluable for selective breeding experiments and for correlational studies of ethanol-related behaviors, the genetically heterogenous (HS) mice, will to be maintained and used by ARC investigators. Over the past 5 years, the ARC has developed, by selective breeding from the HS mice, a unique animal model for the study of acute functional tolerance (AFT). The Animal Core will continue to selectively breed for the high (HAFT) and low (LAFT) lines and will produce sufficient numbers of these mice, at each generation of selection, to meet the needs of the ARC investigators. In addition we propose to conduct several generations of selective breeding for lines of mice that differ in very rapid acute functional tolerance (VRAFT) to ethanol. Finally, as specific loci for genes that mediate differences in sensitivity and tolerance to ethanol are identified, the Animal Core will assist in selective breeding mice by genotype; thus, producing for ARC investigators congenic strains differing only at specified loci, e.g. at quantitative trait loci for ethanol sensitivity.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Specialized Center (P50)
Project #
2P50AA003527-21
Application #
6267056
Study Section
Project Start
1997-12-01
Project End
1998-11-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
21
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Bennett, B; Carosone-Link, P; Beeson, M et al. (2008) Genetic dissection of quantitative trait locus for ethanol sensitivity in long- and short-sleep mice. Genes Brain Behav 7:659-68
Vasiliou, Vasilis; Ziegler, Thomas L; Bludeau, Pequita et al. (2006) CYP2E1 and catalase influence ethanol sensitivity in the central nervous system. Pharmacogenet Genomics 16:51-8
Bowers, Barbara J; Miyamoto-Ditmon, Jill; Wehner, Jeanne M (2006) Regulation of 5-HT2A/C receptors and DOI-induced behaviors by protein kinase Cgamma. Pharmacol Biochem Behav 85:441-7
Zimatkin, Sergey M; Pronko, Sergey P; Vasiliou, Vasilis et al. (2006) Enzymatic mechanisms of ethanol oxidation in the brain. Alcohol Clin Exp Res 30:1500-5
Radcliffe, Richard A; Bludeau, Pequita; Asperi, William et al. (2006) Confirmation of quantitative trait loci for ethanol sensitivity and neurotensin receptor density in crosses derived from the inbred high and low alcohol sensitive selectively bred rat lines. Psychopharmacology (Berl) 188:343-54
Smith, Amy M; Bowers, Barbara J; Radcliffe, Richard A et al. (2006) Microarray analysis of the effects of a gamma-protein kinase C null mutation on gene expression in striatum: a role for transthyretin in mutant phenotypes. Behav Genet 36:869-81
Bowers, Barbara J; Radcliffe, Richard A; Smith, Amy M et al. (2006) Microarray analysis identifies cerebellar genes sensitive to chronic ethanol treatment in PKCgamma mice. Alcohol 40:19-33
Haughey, Heather M; Kaiser, Alan L; Johnson, Thomas E et al. (2005) Norepinephrine transporter: a candidate gene for initial ethanol sensitivity in inbred long-sleep and short-sleep mice. Alcohol Clin Exp Res 29:1759-68
Wu, Peter H; Poelchen, Wolfgang; Proctor, William R (2005) Differential GABAB Receptor Modulation of Ethanol Effects on GABA(A) synaptic activity in hippocampal CA1 neurons. J Pharmacol Exp Ther 312:1082-9
Quertemont, Etienne; Eriksson, C J Peter; Zimatkin, Sergey M et al. (2005) Is ethanol a pro-drug? Acetaldehyde contribution to brain ethanol effects. Alcohol Clin Exp Res 29:1514-21

Showing the most recent 10 out of 355 publications