Alcohol action on extended amygdala glutamate synapses
Alcohol action on extended amygdala glutamate synapses
批准号:
8265728
负责人:
DANNY G WINDER
金额:
$35.61万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-01 至 2015-04-30
关键词:
AcuteAdaptive BehaviorsAgonistAlcohol abuseAlcohol consumptionAlcohol withdrawal syndromeAlcoholismAlcoholsAmygdaloid structureAnatomyAnxietyBehaviorBrainBrain regionCell NucleusCharacteristicsChronicComplexCorticotropin-Releasing Hormone ReceptorsDataDependenceDevelopmentDiffuseDopamineEnvironmentEthanolFrightGeneticGlutamatesHealthIndividualKindling (Neurology)Knock-outKnockout MiceLiteratureLong-Term PotentiationMaintenanceMidbrain structureMolecularMusN-Methyl-D-Aspartate ReceptorsNatureNeuronsParticipantPituitary GlandPlayProcessPropertyReceptor SignalingRecruitment ActivityResearch PersonnelRewardsRoleSeriesSignal TransductionSignaling MoleculeSocietiesStimulusStressStructure of terminal stria nuclei of preoptic regionSynapsesSynaptic plasticitySystemTestingTreatment ProtocolsViralWorkaddictionalcohol abuse therapyalcohol behavioralcohol effectalcohol exposurealcohol sensitivitydrinkingdrinking behaviorextracellularinsightneuroadaptationpublic health relevancereceptor functionresearch studyresponsespecies differencestemstressortherapeutic developmenttooltransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Alcoholism is a tremendous health and financial burden on our society. A growing literature indicates that a series of interconnected brain regions referred to as the extended amygdala plays a key role in alcohol-related behaviors. In isolated studies, we and others have identified adaptations that occur at synapses in these regions in response to acute and chronic ethanol exposure. Here, we propose experiments to in parallel examine key points in this circuitry for their responses to a common alcohol treatment regimen, to better determine the concerted effects of ethanol and ethanol withdrawal. Moreover, we will assess molecular mechanisms involved in these actions through the use of a new conditional knockout mouse for the NMDA receptor subunit NR2B combined with a viral-directed knockout strategy. In total, the proposed work will begin to define specific mechanisms likely to play key roles in pathological adaptations and behaviors associated with chronic alcohol intake, thus providing new potential opportunities for therapeutic development.
PUBLIC HEALTH RELEVANCE: Alcoholism poses an enormous health and financial burden on our society. Currently, our understanding of the brain circuitries involved in alcoholism is far from complete. The successful completion of these proposed studies will result in important new information about neurons that may be involved in alcoholism, potentially creating new targets for therapeutics development.
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依托单位:
海外基金