Elucidating electrical stimulation induced non-neuronal activity using emerging in vivo imaging technology and electrophysiology
Elucidating electrical stimulation induced non-neuronal activity using emerging in vivo imaging technology and electrophysiology
批准号:
10267211
负责人:
Takashi Daniel Yoshida Kozai
金额:
$60.45万
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:
未结题
起止时间:
2020-09-30 至 2025-06-30
关键词:
2&apos,3&apos-Cyclic-Nucleotide PhosphodiesterasesAstrocytesAutomobile DrivingBasic ScienceBehaviorBiologyBiophysicsBlood VesselsBlood flowBrainCalciumCell Differentiation processCell LineageCellsChargeChemicalsChronicClinicalCoupledDatabasesDegenerative DisorderDevelopmentDevice DesignsDiseaseDsRedElectric StimulationElectrodesElectrophysiology (science)EventForeign BodiesFrequenciesFutureHealthHealth StatusImageImaging TechniquesImaging technologyImmuneImmunohistochemistryInjuryInterventionInvestigationMental DepressionMicroelectrodesMicrogliaMolecularMonitorMorphologyMusMyelogenousNerve RegenerationNeurogliaNeuronsNeurosciencesNeurosciences ResearchOligodendrogliaOpticsParkinson DiseasePatientsPericytesPeriodicityPersonal SatisfactionPhasePhotic StimulationPhysiologicalPrevalencePropertyProtein AnalysisRNA analysisRecommendationRegenerative MedicineResearchSafetySensorySignal TransductionSmooth Muscle MyocytesSpectrum AnalysisStimulusSupporting CellTechniquesTherapeuticTimeTissuesTransgenic AnimalsVascular Smooth MuscleVasodilationVisual CortexWorkangiogenesisbrain cellbrain tissueclinical applicationclinical implementationdesignelectric impedanceelectrical microstimulationexcitotoxicityimaging approachimaging platformimplantable deviceimplantationimprovedin vivoin vivo imagingmicrostimulationmultiphoton imagingmyelinationneural networkneuronal excitabilityneuroregulationneurovascular couplingoligodendrocyte progenitorpredictive modelingprogenitorratiometricresponsesensorspatiotemporalstem cellstissue repairvasoconstrictionvoltage
中文摘要
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英文摘要
Project Summary
Electrical microstimulation has become a mainstay of fundamental neuroscience exploration and an
increasingly prevalent clinical therapy. Despite the growing prevalence of neuromodulation therapies, the
fundamental physiological and mechanistic properties driving the beneficial effect for the patient are poorly
understood. This R01 application aims to greatly improve our understanding of how different non-neuronal
cells (myeloid lineage, oligodendrocyte progenitor lineage, and vascular smooth muscle cells) respond and
contribute to the electrical stimulation response. Understanding of the relationship between stimulation
parameters and supporting non-neuronal cell activity, including blood flow, will help determine the impact of
electrical microstimulation on chronic circuit behavior in-vivo over time. In this proposal, we use leading-edge in
vivo multiphoton imaging techniques with multiple transgenic animals to systematically evaluate the
relationship between stimulation parameters and the induced changes over time at the molecular, cellular, and
local network. An improved understanding of the impact of electrical microstimulation on the overall tissue
health, changes to the foreign body response, stimulation of tissue repair, and safety limits will help inform
improved stimulation paradigms and device design for therapeutic applications and basic neuroscience
research.
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