Genes and molecular pathways in nicotine dependence and withdrawal
Genes and molecular pathways in nicotine dependence and withdrawal
批准号:
8598866
负责人:
M. Imad Damaj
金额:
$30.5万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2017-12-31
关键词:
Animal GeneticsAnimal ModelAreaBehaviorBehavioralBehavioral GeneticsBioinformaticsBrainBrain regionCandidate Disease GeneCessation of lifeCigaretteComplexDataData SetDiseaseDominant-Negative MutationEtiologyGene ExpressionGenesGeneticGenetic screening methodGenomeGenomicsHealthHumanHuman GeneticsInbred Strains MiceInbreedingIndividualLiteratureMapsMeasurementModelingMolecularMolecular ProfilingMusNeurobiologyNicotineNicotine DependenceNicotine WithdrawalNicotinic ReceptorsPathway interactionsPharmacologyPhenotypePredispositionQuantitative Trait LociRecombinantsRelapseReportingResearch PersonnelRewardsRiskSamplingSeveritiesSignal TransductionSmokeSmokerSmokingSourceTestingTobacco smokingTranslationsTwin Multiple BirthVariantViral VectorVirginiaWithdrawaladeno-associated viral vectorbasebehavioral genomicscandidate markercase controldata miningdatabase of Genotypes and Phenotypesdesigngenetic analysisgenetic linkage analysisgenetic manipulationgenome wide association studymouse modelpublic health relevanceresponserisk variantskillssmall hairpin RNAsmoking cessationtrait
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Despite evidence of strong genetic contributions to the etiology of smoking initiation (SI) and nicotine dependence (ND), we are far from identifying the specific genetic basis of individual susceptibility to ND. This project - to deepen our understanding of how genes contribute to risk for nicotine dependence (ND) - has arisen as an effort to utilize maximally the relatively unique and complementary set of skill of this group of investigators in complex human genetics, animal genetics and nicotine pharmacology. We will validate these putative risk genes using a two-step approach: replication in other human samples and the demonstration in animal models of ND that variants in these genes contribute to neurobiological pathways likely involved in ND. We will first identify promising candidate genes for smoking initiation (SI) and ND by data-mining GWA datasets and the selected candidates will be replicated. Using a mouse model of nicotine withdrawal, we will characterize behavioral QTLs relevant for ND using a recently developed expanded BXD RI mouse strain panel, focusing on strains informative for already identified areas of provisional QTLs. This approach allows us to both validate and refine our mapping of the nicotine behavioral QTL. Furthermore, we will identify candidate genes for ND by combining expression and behavioral genetics analyses in these BXD RI mouse strains. Candidate genes/pathways identified and prioritized from human and mouse studies will be validated by pharmacological or genetic manipulations to alter expression or function of candidate genes in mouse brain and determine effects on behavioral responses to in models of nicotine reward and withdrawal.
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依托单位:
海外基金