Adolescent Alcohol and GABAergic Neurotransmission in the Adult Prefrontal Cortex
Adolescent Alcohol and GABAergic Neurotransmission in the Adult Prefrontal Cortex
批准号:
8649613
负责人:
Samuel William Centanni
金额:
$4.22万
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:
2013-09-30 至 2015-09-29
关键词:
AbstinenceAcuteAddressAdolescenceAdolescentAdultAgonistAlcohol consumptionAlcoholsAnimal ModelAttenuatedBehaviorBehavior ControlBehavioralBiochemicalBrainBrain regionBreathingCellsCognitiveCognitive deficitsControlled StudyDataDecision MakingDevelopmentEthanolExhibitsImmunoblottingImpulsivityIntoxicationKnowledgeMeasuresMediatingModelingNeurobiologyNeurodevelopmental DisorderNeuronsNeurotransmittersPatternPhenotypePlasticsPlayPrefrontal CortexProcessPropertyPublic HealthRattusRisk-TakingRoleSchizophreniaSliceSynapsesSystemTestingTrainingadolescent alcoholadolescent alcohol abuseadolescent alcohol exposurealcohol exposureattenuationbasecareer developmentcognitive controlcognitive functioncritical periodemerging adultexecutive functionflexibilityhippocampal pyramidal neuroninsightneurodevelopmentneurosteroidsneurotransmissionnovelpatch clamppublic health relevancereceptorresearch studyunderage drinkingvapor
中文摘要
描述(由申请人提供):前额叶皮层(PFC)被认为在受酒精暴露负面影响的认知过程中起重要作用。与其他大脑区域相比,PFC的神经元连接在青春期经历了一个重组和完善的关键时期,这与认知控制和决策能力的提高是一致的。在此期间发生的环境损害可能对前额叶皮层造成特别大的损害,导致神经发育异常,并对认知功能产生长期影响,对决策和行为控制产生负面影响。对酒精的尝试通常始于青春期,那时人们经常会像酗酒一样过度饮酒,导致高度醉酒的循环,随后是短暂的戒酒。本研究将研究青春期酗酒对pfc中GABAA受体介导的神经传递发育的影响。强有力的初步数据表明,在青春期暴露于酒精的成年大鼠中,由突触外δ -GABAA型受体调节的特定张力电流减少。我们假设这会损害pfc的认知功能。另外的初步数据也支持了这一假设,该数据显示,在青春期接触酒精的成年大鼠在操作性设置转移任务中表现出行为灵活性的下降。本研究将采用生物化学、电生理和行为学方法来研究青少年酒精滥用对gaba能神经传递和认知功能发展的影响,特别是对成人PFC行为灵活性的影响。该研究的主要假设是,青少年酗酒会导致成人PFC中gaba能神经传递和认知功能的发育中断。所提出的研究和相关的训练计划不仅将促进申请人的职业发展,而且从这些研究中获得的结果将大大促进我们对青少年酒精滥用对成人前额叶功能和行为认知控制的长期影响的理解。
英文摘要
DESCRIPTION (provided by applicant): The prefrontal cortex (PFC) is thought to play an important role in the cognitive processes that are negatively impacted by alcohol exposure. Compared to other brain regions, the neuronal connections of the PFC undergo a critical period of reorganization and refinement during adolescence and this coincides with improvement in cognitive control and decision making. Environmental insults that occur during this period may be particularly damaging to prefrontal cortex, resulting in aberrant neurodevelopment along with long-lasting effects on cognitive functioning that negatively impacts decision-making and behavioral control. Experimentation with alcohol typically begins during adolescence when it is often consumed in excessive binge-like episodes resulting in a cycle of very high levels of intoxication followed by a short period of abstinence. This proposal will examine the effects of binge-like adolescent alcohol exposure on development of GABAA receptor-mediated neurotransmission in the PFC. Strong supportive preliminary data is presented that suggests that a specific tonic current regulated by extrasynaptic delta-GABAA-type receptors is reduced in adult rats exposed to alcohol during adolescence, and we hypothesize that this will impair cognitive function of the PFC. This is supported by additional preliminary data showing that adult rats exposed to alcohol during adolescence exhibited decreases in behavioral flexibility on an operant set-shifting task. This proposal will use biochemical, electrophysiological and behavioral approaches to examine the effect of adolescent alcohol abuse on the development of GABAergic neurotransmission and cognitive function and in particular, behavioral flexibility of the adult PFC. The overarching hypothesis of this proposal is that binge-like alcohol exposure during adolescence results in disruption of development of GABAergic neurotransmission in the adult PFC and cognitive function. The proposed studies and related training plan will not only further the career development of the applicant, but the results obtained from these studies will significantly advance our understanding of the long- term consequences of adolescent alcohol abuse on prefrontal function and cognitive control of behavior in the adult.
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会议论文
Insular cortex-BNST neural circuit regulation of chronic alcohol abstinence-induced negative affect
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批准号:10557905
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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:2021
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负责人:Samuel William Centanni
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依托单位:
Delineating sex-specific abstinence-induced negative affective behavior in insular circuitry
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批准号:10732894
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项目类别:
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资助金额:$4.87万
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财政年份:2021
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负责人:Samuel William Centanni
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依托单位:
Insular Cortex-BNST neural circuit regulation of chronic alcohol abstinence-induced negative affect
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批准号:9976199
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项目类别:
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资助金额:$14.97万
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财政年份:2020
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负责人:Samuel William Centanni
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依托单位:
Adolescent Alcohol and GABAergic Neurotransmission in the Adult Prefrontal Cortex
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批准号:8773186
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项目类别:
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资助金额:$3.71万
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财政年份:2013
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负责人:Samuel William Centanni
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依托单位:
海外基金