A critical role for rapid estrogen signaling in alcohol addiction and anxiety
A critical role for rapid estrogen signaling in alcohol addiction and anxiety
批准号:
10013109
负责人:
Kristen Elizabeth Pleil
金额:
$46.59万
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:
已结题
起止时间:
2019-09-10 至 2024-06-30
关键词:
AcuteAdoptedAlcohol consumptionAlcohol dependenceAlcohol withdrawal syndromeAlcoholsAmygdaloid structureAnatomyAnxietyAnxiety DisordersAutomobile DrivingBehaviorBehavior ControlBehavioralBehavioral MechanismsBiological AvailabilityBiosensorBrainCalciumCell NucleusCellsCorticotropin-Releasing HormoneDataDiseaseDoseDrug usageE211Electrophysiology (science)EstradiolEstrogen ReceptorsEstrogensEstrusExperimental DesignsFemaleFiberGlutamatesGonadal Steroid HormonesHormonesImageIn Situ HybridizationInterneuron functionLasersLeadMass Spectrum AnalysisMeasuresMembraneMenstrual cycleNeuronsNeuropeptidesOpticsOutputPeriodicityPeripheralPharmacologyPhenotypePhotometryPlayPopulationPreventionRNA InterferenceRecording of previous eventsResearchResolutionRiskRisk FactorsRoleSignal TransductionSliceSourceStressStructure of terminal stria nuclei of preoptic regionSynapsesTechnologyTimeWomanWorkaddictionalcohol comorbidityalcohol exposurealcohol use disorderbinge drinkingdrinkingdrinking behaviorexperimental studyin vivomalemennegative affectneural circuitneurophysiologyneuropsychiatric disordernovelnovel therapeuticsoptogeneticsreceptorreceptor bindingrecruitrelating to nervous systemreproductiveresponsesensorsexstress reactivitystressorsynaptic functiontooltransmission process
中文摘要
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英文摘要
Project Summary/Abstract
Binge alcohol drinking and high stress reactivity are leading risk factors for anxiety and alcohol use disorders,
and women are at twice the risk for co-expression of these diseases. The sex hormone estrogen has been
implicated in playing a modulatory role in anxiety and alcohol/drug use and may be related to the telescoping
of addiction observed in women by amplifying the positive and negative components of binge alcohol
consumption and withdrawal. Further, alcohol consumption itself may be able to stimulate estrogen synthesis
to promote drinking behavior, suggesting that estrogen signaling may be an important mechanism in addiction
for both males and females. However, the mechanisms by which estrogen regulates neuronal function to
control these behaviors is unknown. We hypothesize that estrogen signals at membrane-bound receptors
located at discrete synaptic nodes of limbic circuitry to modulate their control of behavior, and that this
mechanism is prominent at baseline in females but becomes more important in males across alcohol drinking
exposure. In the proposed work, we examine the locus and mechanism of endogenous estrogen signaling, its
effect on circuit function and corresponding behavior, and alcohol-induced plasticity in estrogen modulation in
both males and females.
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A critical role for rapid estrogen signaling in alcohol addiction and anxiety
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批准号:10190744
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项目类别:
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资助金额:$46.58万
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财政年份:2019
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负责人:Kristen Elizabeth Pleil
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依托单位:
A critical role for rapid estrogen signaling in alcohol addiction and anxiety
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批准号:10447201
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资助金额:$44.04万
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财政年份:2019
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负责人:Kristen Elizabeth Pleil
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财政年份:2015
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The role of excitatory inputs to BNST CRF neurons in alcohol drinking behavior
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批准号:9379322
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项目类别:
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资助金额:$11.26万
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财政年份:2015
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依托单位:
The role of excitatory inputs to BNST CRF neurons in alcohol drinking behavior
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批准号:9461824
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项目类别:
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资助金额:$24.9万
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财政年份:2015
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依托单位:
The effect of alcohol drinking on NPY modulation of inhibition in the BNST
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批准号:8469284
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项目类别:
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资助金额:$5.22万
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财政年份:2012
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负责人:Kristen Elizabeth Pleil
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依托单位:
The effect of alcohol drinking on NPY modulation of inhibition in the BNST
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批准号:8314809
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项目类别:
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资助金额:$4.92万
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财政年份:2012
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负责人:Kristen Elizabeth Pleil
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依托单位:
海外基金