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Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence.

Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Research Abstract Details 

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  • Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Abstract Text:

    a a palmerA A Palmer,c n lessov-schlaggarC N Lessov-Schlaggar,c a ponderC A Ponder,c s mckinnonC S McKinnon,t j phillipsT J Phillips,

    Previous studies have suggested that common genetic mechanisms influence sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone. We conducted two quantitative trait locus (QTL) studies to identify chromosomal regions that harbor genes that influence locomotor response to ethanol (2 g/kg) and allopregnanolone (17 mg/kg) using F2 crosses between C57BL/6J and DBA/2J mice. Because our previous data from the BXD recombinant inbred strains had indicated that chromosome 2 contained QTL for sensitivity to the locomotor-stimulant effects of both ethanol and allopregnanolone, we also tested reciprocal chromosome 2 congenic strains for sensitivity to the locomotor-stimulant effects of both drugs. The F2 analysis for ethanol sensitivity identified significant QTL on chromosomes 1 and 2 and suggestive QTL on chromosomes 5 and 9. The analysis of the allopregnanolone F2 study identified suggestive QTL on chromosomes 3, 5 and 12. Suggestive evidence for a female-specific QTL on chromosome 2 was also found. The studies of congenic mouse strains indicated that both the congenic strains captured one or more QTL for sensitivity to the locomotor-stimulant effects of both ethanol (2 g/kg) and allopregnanolone (17 mg/kg). When Fisher's method was used to combine the P values for the RI, F2 and congenic studies of the chromosome 2 QTL, cumulative probability scores of 9.6 x 10(-15) for ethanol and 7.7 x 10(-7) for allopregnanolone were obtained. These results confirm the presence of QTL for ethanol and allopregnanolone sensitivity in a common region of chromosome 2 and suggest possible pleiotropic genetic influence on sensitivity to these drugs.

    Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Publishing Authors By Initials

    aa palmerAA Palmer,cn lessov-schlaggarCN Lessov-Schlaggar,ca ponderCA Ponder,cs mckinnonCS McKinnon,tj phillipsTJ Phillips,

    For similar genetic structures: genome: genome components: genes: quantitative trait loci research abstracts see: genetic structures: genome: genome components: genes: quantitative trait loci research

    PUBMED ID PMID:

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    Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Genes, brain, and behavior

    VOLUME: 5

    Page Numbers: 506-17

    Journal Abbreviation: Genes Brain Behav.

    ISSN: 1601-1848

    DAY: 3

    MONTH: Oct

    YEAR: 2006

    Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101129617

    Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Keywords Mesh Terms:

    KEYWORDS: Quantitative Trait Loci

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Information

    Substance Name: Ethanol

    Registry Number: 64-17-5

    Grant and Affiliation Information for Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence.

    AFFILIATION: Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA. aap@uchicago.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIMH

    GRANT: MH70933

    ACRONYM: MH

    MEDLINETA: Genes Brain Behav

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    DATABASENAME:

    ACCESSION NUMBER:

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