grant

Understanding the functional anatomy of nociceptive spinal output neurons

Organization UNIVERSITY OF PITTSBURGH AT PITTSBURGHLocation PITTSBURGH, UNITED STATESPosted 1 Jul 2023Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY20252-photonAffectAffectiveAnatomic SitesAnatomic structuresAnatomyAssayBehaviorBehavior monitoringBehavioralBehavioral AssayBilateralBioassayBiological AssayBrainBrain Nervous SystemCalciumCell Communication and SignalingCell NucleusCell SignalingClinical TreatmentContralateralDREADDsDataDevelopmentEncephalonFutureGeneticGoalsImageIntracellular Communication and SignalingInvestigatorsIpsilateralKnowledgeLaser Scanning Confocal MicroscopyMediatingMedulla SpinalisMentorsMesencephalic Central GrayMidbrain Central GrayModelingNerve CellsNerve Impulse TransmissionNerve TransmissionNerve UnitNeural CellNeurocyteNeuronal TransmissionNeuronsNociceptionNucleusOpticsOutputPainPain ControlPain TherapyPain managementPainfulPathway interactionsPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatternPeriaqueductal GrayPersonsPhysiciansPlayPopulationPreparationPropertyQOLQuality of lifeResearch PersonnelResearchersRoleScientistSideSignal TransductionSignal Transduction SystemsSignalingSpinalSpinal CordStimulusStructureTechnical ExpertiseTestingThalamic structureThalamusTherapeuticTherapeutic InterventionTrainingTransmissionViralannulus of the aqueductaxon signalingaxon-glial signalingaxonal signalingbehavior responsebehavioral monitoringbehavioral responsebiological signal transductioncareercell typecellular targetingchronic painclinical interventionclinical research siteclinical siteclinical therapyconfocal scanning microscopydesigner receptors exclusively activated by designer drugsdetectordetermine efficacydevelopmentaldorsal hornefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationevaluate efficacyexamine efficacyexperimentexperimental researchexperimental studyexperimentsgene manipulationgenetic manipulationgenetically manipulategenetically perturbglia signalingglial signalingimagingimproved outcomeintervention therapymidbrain central gray substancenerve signalingneural circuitneural circuitryneural signalingneurocircuitryneuronalneuronal patterningneuronal signalingneurotransmissionnew drug targetnew druggable targetnew pharmacotherapy targetnew therapeutic targetnew therapy targetnociceptivenovelnovel drug targetnovel druggable targetnovel pharmacotherapy targetnovel therapeutic targetnovel therapy targetopticalpain interventionpain signalpain treatmentparabrachial nucleuspathwaypatient oriented outcomesperiaqueductal gray matterpreparationsresponsesocial rolesomatosensorysynaptic circuitsynaptic circuitrytechnical skillsthalamictooltransmission processtrial regimentrial treatmenttwo-photonvirtual
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Full Description

Project Summary/Abstract
Pain is a debilitating condition that severely impacts quality of life. Despite a growing need for new treatments,

an incomplete understanding of the neural circuitry underlying pain has limited the development of novel pain

therapeutics. Spinal projection neurons in the superficial dorsal horn channel pain signals from the spinal cord

into the brain. These neurons may represent a viable target for future pain management strategies. While virtually

all the spinal output neurons mediating nociception target the contralateral parabrachial nucleus, subsets of

these neurons also project to other supraspinal structures, such as the ipsilateral parabrachial nucleus (spino-

PBN neurons) or the contralateral periaqueductal gray (spino-PAG neurons). Given the distinct collateralization

patterns of these neurons, I hypothesize that the spino-PBN and spino-PAG neurons have distinct

nociceptive functions. I will test this hypothesis using anatomical (Aim 1), functional (Aim 2), and behavioral

(Aim 3) approaches. Aim 1 will characterize the projection patterns of the spino-PAG and spino-PBN neurons

through retrograde viral tracing, optical clearing, and ribbon scanning confocal microscopy. Aim 2 will determine

the functional response properties of the spino-PAG and spino-PBN neurons using two-photon calcium imaging

and natural stimuli applied to an ex vivo preparation. Aim 3 will uncover the role of the spino-PAG and spino-

PBN neurons in mediating nocifensive behavior using chemogenetics and behavioral assays of nociception. The

experiments described in this proposal have the potential to advance our basic understanding of the spinal output

circuitry mediating nociception and help determine the efficacy of spinal projection neurons as new targets for

clinical intervention. To complete this proposal, I will receive rigorous intellectual and technical training from a

team of expert scientist and clinician mentors. This training will enable me to become an independent

investigator, allowing me to accomplish my long-term goal of becoming a physician-scientist specializing in pain.

Grant Number: 5F31NS134315-03
NIH Institute/Center: NIH

Principal Investigator: Isabel Bleimeister

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