Inhibitory synaptic plasticity during learning
Inhibitory synaptic plasticity during learning
批准号:
10270121
负责人:
ALISON L BARTH
金额:
$52.69万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-09-30 至 2022-08-31
关键词:
AcuteAddressAnatomyAnimalsAreaAssociation LearningBehaviorBehavioralBrainCellsCerebral cortexCharacteristicsChemosensitizationCholinergic ReceptorsClimactericClustered Regularly Interspaced Short Palindromic RepeatsComplexCortical ColumnCoupledCouplingDataDisinhibitionElectrophysiology (science)EsthesiaHome environmentImageInhibitory SynapseInterneuronsLearningMediatingMemoryMethodsModificationMusNeocortexNeuronal PlasticityNeuronsOutcomeOutputParvalbuminsPathway interactionsPsychological reinforcementPublishingRewardsSensorySignal TransductionSliceSomatosensory CortexStimulusSynapsesSynaptic plasticitySystemTactileTestingThalamic structureTimeTrainingTransgenic MiceVariantWaterbasecell typecholinergicclassical conditioningexperienceexperimental studyin vivoknock-downneocorticalneural circuitprogramsrelating to nervous systemresponsesensory cortexsensory inputsensory stimulussynaptic inhibition
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Abstract
What are the neural circuits by which the brain differentiates between incidental and meaningful
environmental inputs to enable long-lasting changes in sensation and behavior? Experimental
evidence indicates that this distinction may be made at the earliest stages of cortical processing,
in primary sensory cortex. Here we will use high-throughput, automated behavioral training in
freely-moving mice to determine how the detailed neural circuitry of the cerebral cortex is
distinctly changed during acquisition of a tactile reward-based association. Our preliminary data
indicate that long-lasting modifications in parvalbumin (PV)-mediated synaptic inhibition is
selectively driven by sensory association training but not passive sensory exposure, providing a
foothold to investigate the cellular circuitry that distinguishes between different types of
experience-dependent plasticity. Using in vivo Ca imaging, targeted electrophysiological
recordings and anatomical analyses, we will determine the mechanisms by which specific
neural subtypes facilitate learning-related reorganization of the cortical column.
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依托单位:
海外基金