Adolescent alcohol drinking and GABA signaling
Adolescent alcohol drinking and GABA signaling
批准号:
10598055
负责人:
Kevin J Bender
金额:
$40.04万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
未结题
起止时间:
2019-04-12 至 2025-03-31
关键词:
AKT Signaling PathwayAcuteAdolescenceAdolescentAdultAffectAgeAlcohol abuseAlcohol consumptionAlcohol dependenceAlcoholsAxonBehaviorBehavioralBrainCell physiologyCellsChloridesComplementDataDecision MakingDevelopmentDiseaseElectrophysiology (science)EtiologyExecutive DysfunctionExploratory BehaviorFunctional disorderGlutamatesGoalsHeavy DrinkingImageIndividualInterneuron functionLifeLong-Term EffectsMaintenanceMediatingMolecularMusMyoepithelial cellNeuronsOpticsPI3K/AKTParvalbuminsPatternPerinatalPredispositionPrefrontal CortexPrincipal InvestigatorPropertyProto-Oncogene Proteins c-aktPyramidal CellsRNA InterferenceRegulationRisk AssessmentRisk TakingRodentSignal TransductionSiteSliceSubstance abuse problemSynapsesTechniquesTestingTherapeutic InterventionTimeViralWorkadolescent alcohol exposurealcohol effectalcohol riskalcohol use disorderalcohol use initiationcellular targetingcombatcritical perioddrinkingdrinking behaviorexecutive functiongamma-Aminobutyric Acidinfancyinhibitory neuroninsightmature animalnervous system disordernew therapeutic targetnovel therapeutic interventionperiadolescentpharmacologicpostsynapticpostsynaptic neuronspreadolescencepreventproblem drinkersodium-potassium-chloride cotransporter 1 proteinsynaptic functiontherapeutic targettwo-photonunderage drinking
中文摘要
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英文摘要
PROJECT SUMMARY
Adolescence marks a period of increased risk taking and exploration. As part of this exploratory behavior,
many individuals initiate alcohol use during adolescence, which can lead to increased risk for alcohol use
disorders later in life. One major site of adolescent maturation in prefrontal cortex are GABAergic inhibitory
neurons, including parvalbumin positive chandelier cells. Chandelier cells synapse directly onto the axon
potential initiating sites of neighboring glutamatergic pyramidal cells. They are therefore uniquely poised to
regulate pyramidal cell spiking. Here, our goal is to understand how the function of these two inhibitory cell
classes are affected by adolescent alcohol consumption, and to determine if manipulations to chloride
transporter function alters drinking behavior. We will use a combination of electrophysiology and 2-photon
imaging to understand how interneuron function is regulated at the cellular level, and viral manipulation of
chloride transporter function paired with behavior to understand how prefrontal inhibitory function regulates
drinking. Results of this study will provide insight into how inhibitory circuits contribute to drinking behavior
and may elucidate potential therapeutic targets to treat alcohol abuse disorders.
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会议论文
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财政年份:2013
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Function and regulation of action potential bursts in the auditory system.
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依托单位:
海外基金