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Molecular Basis of Excessive Alcohol Drinking

Molecular Basis of Excessive Alcohol Drinking
过量饮酒的分子基础
批准号:
7534922
负责人:
SUSAN E. BERGESON
金额:
$23.5万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-27 至 2011-08-31
关键词:
AbstinenceAcuteAffectAlcohol consumptionAlcohol dependenceAlcohol withdrawal syndromeAlcoholismAlcoholsAnimal ModelAnimalsApoptosisBackcrossingsBehavioralBiological AssayBoutosBrainBrain regionCandidate Disease GeneCategoriesChromosomes, Human, Pair 9ChronicCollaborationsComplexCongenic MiceControl AnimalCore FacilityDNA Methyltransferase 3BDataData AnalysesData SetDatabasesDepositionDiseaseDissectionDown-RegulationEnvironmental Risk FactorEpigenetic ProcessEthanol MetabolismExcisionFemaleFundingGene ExpressionGene Expression ProfileGene ProteinsGene SilencingGenesGeneticGenetic ModelsGenetic Predisposition to DiseaseGenotypeGoalsHeavy DrinkingHistonesHybridsImmunohistochemistryIn Situ HybridizationInternetKnock-outKnockout MiceKnowledgeLaboratoriesLeadLocalizedManuscriptsMapsMediatingMeta-AnalysisMicroRNAsMicroarray AnalysisModelingModificationMolecularMorbidity - disease rateMusNumbersOnline SystemsOntologyPathway AnalysisPhenotypePlayPreventionPrincipal InvestigatorPromoter RegionsProteomicsProtocols documentationPublicationsQuantitative Trait LociRNARNA InterferenceRattusRegulationReportingResearchResearch PersonnelReverse Transcriptase Polymerase Chain ReactionRiversRoleSamplingScientistSiteStandards of Weights and MeasuresSystemTestingTimeTranscriptTransgenic MiceTranslatingValidationViralWeekWithdrawalalcohol abuse therapyalcohol effectalcohol exposurealcohol researchalcohol responsebasebehavior testbrain tissuecDNA Arrayscell typechromatin remodelingcongenicdesigndrinkingendophenotypefallsfollow-uphuman mortalityin vivoinnovationinsightinterestmalemouse modelneuroadaptationopen sourcepreferenceprogenitorprogramspromoterresearch studyresponsesmall hairpin RNAsuccesstrait

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DESCRIPTION (provided by applicant): Alcoholism, a disease of considerable morbidity, mortality and human suffering worldwide, is first and foremost characterized by excessive alcohol drinking. The "Two-Hit hypothesis" that both genetic and environmental factors contribute to excessive alcohol intake is the overarching focus of our current and proposed INIA research. Microarray results from our present UO1 funding have allowed substantial inroads to be made into the understanding of both the genetic predisposition to drink and the molecular consequences of alcohol exposure. Significant candidate genes have been identified though the overlap of several of our own studies and importantly across INIA collaborations. A large searchable, open source web-base database system containing over 30 million microarray data points from our studies was created to make sharing all data within and beyond the alcoholism research field facile (publicly announced in Bergeson et al., 2005). Our current objectives are to continue to build our array database to include expression analyses of six new INIA mouse models, focus us on characterizing candidate genes that fit our "two-hit hypothesis", and to use genetically altered mice and brain region specific viral mediated trans- gene and shRNA expression to test bi-directional expression (up and down regulation) effects on alcohol drinking. We will perform neurocirciutry specific microarray studies following viral-mediated gene changes in the presence and absence of alcohol drinking to better understand anatomical and molecular contributions to excessive alcohol drinking. Finally, initial studies focused on the role of miRNA and chromatin remodeling in alcohol drinking and/or consequences are proposed.
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Supplement to: Medication Development for the Treatment of Alcohol Use Disorder - U01AA028957
Medication Development for the Treatment of Alcohol Use Disorder
Medication Development for the Treatment of Alcohol Use Disorder
Neuroimmune Interactions in High Alcohol Drinking
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