Individual variation in behavioral response to ethanol may be traced in part to the influence of inheritance, i.e., specific genes. For many behaviors, the genetic influences on ethanol sensitivity may account for as much as half of individual variation: therefore, non-genetic (environmental) sources of influence are also important. The overarching goal of these studies is to assess genetic and environmental influences on ethanol responses in mice, focusing on the interactions between genes and environment. We first propose to explore ethanol intoxication in two behavioral domains, motor coordination/ataxia and learning, using multiple laboratory assays. Our hypothesis is that different constellations of genes affect different tasks within a domain. We will select from the several ataxia (and learning) tasks those that are practical for use across a wide range of strains and are highly reliable within a single laboratory. We have created a unique facility for conducting identical behavioral tests at two sites (Edmonton, AB; Portland, OR), and this will allow us to identify those tasks that are also highly replicable across laboratories. Tasks that are both reliable and replicable will be used to survey the genetic contributions to each domain and to ethanol sensitivity. This will allow us to identify a smaller set of tasks that together capture a broad range of genetic influences on ethanol sensitivity. Because neuro-adaptation to ethanol is an important contributor to drug dependence, we will also study the genetic bases of acute, rapid, and chronic tolerance to ethanol in the ataxia tasks. Our second goal is to manipulate the environment systematically. We hypothesize that enriched rearing conditions, testing in the circadian light versus dark phase, and the specific experimenter conducting the behavioral tasks will affect results. Furthermore, we hypothesize that responses to environmental manipulations will differ across different strains, i.e., that genes will exert different effects on ethanol sensitivity and tolerance measures in different environments. In the final set of experiments, we will address the practical significance of these findings by exploring selected gene-environment combinations in null mutants and in lines of mice selected for extremes of behavioral sensitivity and/or tolerance to ethanol. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA012714-05
Application #
6943139
Study Section
Alcohol and Toxicology Subcommittee 4 (ALTX)
Program Officer
Egli, Mark
Project Start
2000-06-01
Project End
2009-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
5
Fiscal Year
2005
Total Cost
$420,281
Indirect Cost
Name
University of Windsor
Department
Type
DUNS #
207863549
City
Windsor
State
ON
Country
Canada
Zip Code
Bohlen, Martin; Hayes, Erika R; Bohlen, Benjamin et al. (2014) Experimenter effects on behavioral test scores of eight inbred mouse strains under the influence of ethanol. Behav Brain Res 272:46-54
Bohlen, M O; Bailoo, J D; Jordan, R L et al. (2012) Hippocampal commissure defects in crosses of four inbred mouse strains with absent corpus callosum. Genes Brain Behav 11:757-66
Munn, Elizabeth; Bunning, Mark; Prada, Sofia et al. (2011) Reversed light-dark cycle and cage enrichment effects on ethanol-induced deficits in motor coordination assessed in inbred mouse strains with a compact battery of refined tests. Behav Brain Res 224:259-71
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Bailoo, Jeremy D; Bohlen, Martin O; Wahlsten, Douglas (2010) The precision of video and photocell tracking systems and the elimination of tracking errors with infrared backlighting. J Neurosci Methods 188:45-52
Bohlen, Martin; Cameron, Andy; Metten, Pamela et al. (2009) Calibration of rotational acceleration for the rotarod test of rodent motor coordination. J Neurosci Methods 178:10-4
Yan, Reginia H Y; Bunning, Mark; Wahlsten, Douglas et al. (2009) Digit ratio (2Dratio4D) differences between 20 strains of inbred mice. PLoS One 4:e5801
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MacPherson, Peter; McGaffigan, Ruth; Wahlsten, Douglas et al. (2008) Impaired fear memory, altered object memory and modified hippocampal synaptic plasticity in split-brain mice. Brain Res 1210:179-88

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