Routing of SPW-R content via distinct hippocampal output pathways
Routing of SPW-R content via distinct hippocampal output pathways
批准号:
10202754
负责人:
MARK J SCHNITZER
金额:
$44.13万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-25 至 2023-06-30
关键词:
AffectAnatomyBehaviorBehavioralCalciumCrystallizationDependenceDorsalElectrophysiology (science)EmotionalEquine muleEventHeadHeterogeneityHippocampus (Brain)ImageLabelLearningLocationMediatingMemoryMicroscopeMicroscopicMorphologyMusNeuronsOpsinOutputPathway interactionsPatternPerformancePopulationPreparationPyramidal CellsRadialResolutionRouteSiliconTechniquesViralViruscraniumexperimental studyfluorophoreinhibitory neuroninsightmemory consolidationneocorticalnoveloptogeneticspostsynapticpresynapticrecruitsegregationtransmission processvoltage
中文摘要
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英文摘要
As synchronous population events SPW-Rs are strongly implicated in the transmission of intra-
hippocampally stored representations to extra-hippocampal targets, supporting the consolidation of
memory at these targets. The primary hippocampal output originates from CA1 pyramidal cells
(CA1PCs), and CA1PCs with specific cortical and subcortical extra-hippocampal targets are
thought to be differentially distributed along the main hippocampal anatomical axes. In turn, recent
studies demonstrated the presence of a large degree of morphological and functional
heterogeneity within the CA1PC populations along these same hippocampal axes, suggesting the
presence of target-specific functional subdivisions within the hippocampal network. However, the
precise anatomical and functional organization, recruitment mechanisms and behavioral relevance
of SPW-Rs along these extra-hippocampal target-specific subdivisions remain unknown. In Project
4, we will perform an extensive set of new correlational and pertubational experiments which will
provide novel insights into CA1PC target-specific SPW-R organization and function.
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