Understanding the functional anatomy of nociceptive spinal output neurons
Understanding the functional anatomy of nociceptive spinal output neurons
批准号:
10751126
负责人:
Isabel Bleimeister
金额:
$4.77万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-07-01 至 2026-06-30
关键词:
AffectAffectiveAnatomyBehaviorBehavior monitoringBehavioralBehavioral AssayBilateralBiological AssayBrainCalciumCell NucleusClinicalContralateralDataDevelopmentFutureGeneticGoalsImageInterventionIpsilateralKnowledgeLaser Scanning Confocal MicroscopyMediatingMentorsModelingNeuronsNociceptionOpticsOutputPainPain managementPathway interactionsPatient-Focused OutcomesPatternPersonsPhysiciansPlayPopulationPreparationPropertyQuality of lifeResearch PersonnelRoleScientistSideSignal TransductionSpinalSpinal CordStimulusStructureTechnical ExpertiseTestingThalamic structureTherapeuticTherapeutic InterventionTrainingVertebral columnViralbehavioral responsecareercell typecellular targetingchronic painclinical research sitedesigner receptors exclusively activated by designer drugsdetectordorsal hornefficacy evaluationexperimental studygenetic manipulationimproved outcomemidbrain central gray substanceneural circuitneuronal patterningneurotransmissionnew therapeutic targetnovelpain signalparabrachial nucleusresponsesomatosensorytooltransmission processtwo-photonvirtual
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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.
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