ShEEP request for an Inscopix nVoke Integrated Imaging and Optogenetics System
ShEEP request for an Inscopix nVoke Integrated Imaging and Optogenetics System
批准号:
9795729
负责人:
Karunesh Ganguly
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-01-01 至 2019-09-30
关键词:
AnimalsBehaviorBehavioralBrainCellsCodeComputer softwareContractsCorpus striatum structureDataDevelopmentDissectionEnvironmentEquipmentFloorHeadHippocampus (Brain)ImageImplantImplantation procedureIndividualInjuryInterventionInvestigationKnowledgeLabelLearningLocationMaintenanceMemoryMicroscopeMonitorNervous system structureNeurofibrillary TanglesNeuronsPatternPhaseProcessRecoveryResearchResolutionRouteSheepSignal TransductionStrokeStructureSurvivorsSystemTechnologyTherapeutic InterventionTimeTraumatic Brain InjuryUnited StatesVeteransWorkawakecell typecostdata acquisitiondisabilityequipment acquisitionflexibilityinsightlensneurotransmissionnew technologynovel therapeuticsoptogeneticsrelating to nervous system
中文摘要
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英文摘要
Stroke and traumatic brain injury are leading causes of disability among veterans. While there has been
substantial research into understanding mechanisms of recovery, there is a relative dearth of studies that
delineate the contributions of specific cell types, e.g. excitatory and/or inhibitory subtypes. Such
knowledge provides greater insight into the recovery process and can aid the development of targeted
interventions. We request the purchase of the Inscopix nVoke Integrated Imaging and Optogenetics
System to conduct such investigations. The Inscopix miniature microscope platform gives us an edge in
investigating how patterned activity in neuronal ensembles represents information about an individual’s
environment, actions, and memories. A key advantage of this system is the ability to image deep neural
structures (e.g. striatum, hippocampus) through a flexible scope during freely moving behaviors.
Importantly, by monitoring and disrupting activity in the same cells over months, we can gain
unprecedented insights into how neural codes evolve during recovery and with therapeutic interventions.
A critical aspect of this technology is unprecedented monitoring at a single-cell resolution of identified
cell-types; this represents the critical next phase of circuit function dissection.
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科研奖励(0)
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