The Portland Alcohol Research Center (PARC) is focused on the genetics of neuroadaptation to ethanol. Specifically, we apply genetic animal models to assess the genetic underpinnings of alcohol neuroadaptation, and to map genes underlying alcoholism risk. The PARC addresses goals related to etiology and prediction of risk of alcohol abuse, alcoholism, and specific alcohol-related health problems (e.g., withdrawal seizures). The genetic risk and protective markers that we are studying will be of utility in the future prevention of alcoholism. The first theme of the PARC is to use behavioral genomics strategies, through genetic mapping and development of new genetic models, to identify genes underlying ethanol neuroadaptation. This theme is addressed by a highly collaborative network of individuals with differing areas of research expertise, including animal behavior, quantitative and molecular genetics, molecular biology, biochemical and behavioral pharmacology, neuroendocrinology, and neuroanatomy. During the initial 4 years of funding, we have added expertise in bioinformatics, cognitive neuroscience and skeletal genetics. The areas of expertise are exploited to address the other main PARC theme, exploring mechanisms underlying ethanol neuroadaptation. PARC PIs have been training pre- and post-doctoral fellows and medical students in alcoholism and alcohol research for more than 25 years. The PARC Core facilities contribute to the efforts to map influential genes, which are initially identified by location as Quantitative Trait Loci, or QTLs. We are progressing to studies of the localized genes and their functions through sequencing and expression analysis. The unique genetic animals we have produced have served as a resource for investigators within and outside of the Center for many years, and the mapping facility is increasingly being utilized by other investigators. A new Alcohol Dependence Core recognizes the increased need to centralize the production of physically dependent animals for studies within and beyond the PARC.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Specialized Center (P50)
Project #
5P50AA010760-08
Application #
6626418
Study Section
Special Emphasis Panel (ZAA1-DD (01))
Program Officer
Anderson, Sally
Project Start
1995-12-20
Project End
2005-12-31
Budget Start
2003-01-01
Budget End
2003-12-31
Support Year
8
Fiscal Year
2003
Total Cost
$1,800,000
Indirect Cost
Name
Oregon Health and Science University
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Iancu, Ovidiu D; Colville, Alexander; Walter, Nicole A R et al. (2018) On the relationships in rhesus macaques between chronic ethanol consumption and the brain transcriptome. Addict Biol 23:196-205
Purohit, Kush; Parekh, Puja K; Kern, Joseph et al. (2018) Pharmacogenetic Manipulation of the Nucleus Accumbens Alters Binge-Like Alcohol Drinking in Mice. Alcohol Clin Exp Res 42:879-888
Iancu, Ovidiu Dan; Colville, Alex M; Wilmot, Beth et al. (2018) Gender-Specific Effects of Selection for Drinking in the Dark on the Network Roles of Coding and Noncoding RNAs. Alcohol Clin Exp Res :
Aoun, E G; Jimenez, V A; Vendruscolo, L F et al. (2018) A relationship between the aldosterone-mineralocorticoid receptor pathway and alcohol drinking: preliminary translational findings across rats, monkeys and humans. Mol Psychiatry 23:1466-1473
Buck, Kari J; Chen, Gang; Kozell, Laura B (2017) Limbic circuitry activation in ethanol withdrawal is regulated by a chromosome 1 locus. Alcohol 58:153-160
Crabbe, John C; Ozburn, Angela R; Metten, Pamela et al. (2017) High Drinking in the Dark (HDID) mice are sensitive to the effects of some clinically relevant drugs to reduce binge-like drinking. Pharmacol Biochem Behav 160:55-62
Colville, A M; Iancu, O D; Oberbeck, D L et al. (2017) Effects of selection for ethanol preference on gene expression in the nucleus accumbens of HS-CC mice. Genes Brain Behav 16:462-471
Hitzemann, Robert; Oberbeck, Denesa; Iancu, Ovidiu et al. (2017) Alignment of the transcriptome with individual variation in animals selectively bred for High Drinking-In-the-Dark (HDID). Alcohol 60:115-120
Chesler, Elissa J; Gatti, Daniel M; Morgan, Andrew P et al. (2016) Diversity Outbred Mice at 21: Maintaining Allelic Variation in the Face of Selection. G3 (Bethesda) 6:3893-3902
Crabbe, John C; Schlumbohm, Jason P; Hack, Wyatt et al. (2016) Fear conditioning in mouse lines genetically selected for binge-like ethanol drinking. Alcohol 52:25-32

Showing the most recent 10 out of 162 publications