Alcohol and inhibition in the prefrontal cortex
Alcohol and inhibition in the prefrontal cortex
批准号:
8457850
负责人:
Michael Charles Salling
金额:
$4.92万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-30 至 2014-09-29
关键词:
AcuteAdolescenceAdolescentAdultAffectAgeAlcohol abuseAlcohol consumptionAlcoholsAmericanAnimal ModelAnimalsAreaAttentionAwarenessBehaviorBehavior ControlBehavioralBrainBrain regionChronicComplementControl GroupsDataDecision MakingDependenceDepressed moodDevelopmentDiseaseDoseElectrophysiology (science)EpidemiologyFrequenciesFunctional disorderFundingGABA AntagonistsGABA ReceptorGABA-A ReceptorGlycineGlycine ReceptorsGoalsHealthcareIndividualLeadLifeMaintenanceMeasuresMediatingMedicineMembraneMemoryMusNeuraxisNeuronsNeurotransmitter ReceptorNeurotransmittersOutputPathologyPersonal SatisfactionPharmaceutical PreparationsPhysiologicalPhysiological AdaptationPrefrontal CortexProductivityPropertyProtocols documentationPublic HealthRelapseResearchResearch ProposalsRodentSliceSocietiesSubstance abuse problemSynapsesSystemTestingThalamic structureTherapeuticTrainingWhole-Cell RecordingsWorkaddictionalcohol effectalcohol exposurealcohol researchalcohol responsealcohol sensitivityalcohol use disorderbinge drinkingbrain cellchronic alcohol ingestioncostcritical perioddentate gyrusdesigndrinkingfamily structuregamma-Aminobutyric Acidhippocampal pyramidal neuroninhibitor/antagonistneurobiological mechanismneuronal excitabilityneurotransmissionnovelpostnatalpreventreceptorresearch studysubstance abusertherapeutic developmenttransmission processunderage drinkingvoltage clamp
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The consequences of alcohol abuse on the American public are profound, both in terms of individual well-being and impact on the family structure, as well as the enormous cost to society in terms of lost productivity and associated health care expenses. Despite increasing efforts, our understanding of the neurobiological mechanisms that underlie the effects of alcohol and the development of alcohol use disorders remains incomplete. Epidemiological research has pointed to adolescence as a critical period in the development of alcohol disorders. One area of the brain that appears especially vulnerable to the effects of alcohol is the prefrontal cortex (PFC), which remains immature at the onset of adolescence. The PFC is involved in decision- making, memory and impulse control, behaviors that are often disrupted following consumption of alcohol and are believed to underlie long-term addiction. In the PFC, pharmacologically relevant doses of alcohol are known to depress neuronal activity (Tu et al. 2007), but very little is known of its interactions with the inhibitor receptors, GABA and glycine, within the PFC. This is despite the expression of GABA-A receptor subtypes in the PFC (Hoestgaard-Jensen et al. 2010) that mediate tonic inhibition in other brain regions and demonstrate high sensitivity to alcohol (Wei et al. 2004, Jia et al. 2008).
In addition, we note that functional glycine receptors are also present in PFC (Ye et al. 2011) but have received little to no attention. The goal of this research proposal is to examine the pharmacological actions of alcohol on neuronal excitability and on GABA and glycine-mediated synaptic and tonic inhibition in the adolescent PFC, and to determine if chronic alcohol drinking during adolescence leads to specific alterations of inhibition that affect neuronal excitability. Tis information could enhance our understanding of the negative effects of alcohol drinking during adolescence and an increased focus on cellular mechanisms involved can help lead to the development of therapeutic strategies to treat alcohol use disorders.
PUBLIC HEALTH RELEVANCE: Drinking alcohol during adolescence is a major public health concern as it often leads to alcohol and substance abuse disorders later in life. The goal of this proposal is to better understand the effects of alcohol on the adolescent brain which will be accomplished by measuring changes in brain cell activity in animals that drink alcohol during adolescence. Findings from this work will raise awareness on alcohol vulnerability during adolescence and could lead to the development of medicines that treat alcohol use disorders.
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会议论文
ADHD and the influence of adolescent alcohol drinking on cognition and behavior
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批准号:10812071
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项目类别:
-
资助金额:$33.75万
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财政年份:2023
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负责人:Michael Charles Salling
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依托单位:
Prefrontal Pathways Engaged in Excessive Alcohol Consumption
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批准号:10363686
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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:2020
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负责人:Michael Charles Salling
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依托单位:
Prefrontal Pathways Engaged in Excessive Alcohol Consumption
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批准号:10038568
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项目类别:
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资助金额:$15.29万
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财政年份:2018
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负责人:Michael Charles Salling
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依托单位:
Prefrontal Pathways Engaged in Excessive Alcohol Consumption
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批准号:9180506
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项目类别:
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资助金额:$18.07万
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财政年份:2018
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负责人:Michael Charles Salling
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依托单位:
Alcohol and inhibition in the prefrontal cortex
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批准号:8549688
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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:Michael Charles Salling
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依托单位:
Role of CAMKII in ethanol self-administration
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批准号:7810438
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项目类别:
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资助金额:$2.77万
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财政年份:2009
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负责人:Michael Charles Salling
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依托单位:
海外基金