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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
利用新兴的体内成像技术和电生理学阐明电刺激诱导的非神经元活动
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

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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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Modulation of Oligodendrocyte Calcium Activity with ICMS and Melatonin Stimulation
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
2020 Nuroelectronic Interfaces Gordon Research Conference and Gordon Research Seminar
  • 批准号:
    9913124
  • 项目类别:
  • 资助金额:
    $2.0万
  • 财政年份:
    2020
  • 负责人:
    Takashi Daniel Yoshida Kozai
  • 依托单位: