Neuronal subtype-specific plasticity in the acute to chronic pain transition
Neuronal subtype-specific plasticity in the acute to chronic pain transition
批准号:
8518294
负责人:
Michael J Caterina
金额:
$60.3万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-30 至 2017-06-30
关键词:
AcuteAcute PainAdverse effectsAffectAfferent NeuronsAnalgesicsAnatomyAnimalsAttentionBehavioralBiologicalBiological AssayCategoriesChemicalsChronicCutaneousDevelopmentDoseEventHypersensitivityImageryIndividualInjuryLabelMaintenanceMeasuresMechanicsMechanoreceptorsMedicalMethodsMolecularMolecular GeneticsMonitorMusNerveNeuronsNeuropathyNociceptionNociceptorsNon-Steroidal Anti-Inflammatory AgentsOperative Surgical ProceduresOpiatesPainParticipantPatientsPerceptionPeripheralPharmaceutical PreparationsPhysiologicalPopulationPreparationProcessProfessional RolePropertyPublic HealthResolutionRoleSkinSocietiesSpinal CordStagingStimulusStructureTechnologyTissuesToxinTraumatic Nerve InjuryWorkcalcium indicatorcell typecellular targetingchronic neuropathic painchronic paindiphtheria toxin receptorimaging modalityimprovedin vivonerve injuryneuronal cell bodynew technologypainful neuropathyprotein expressionresearch studyresponseselective expressionspatiotemporaltool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Inadequate treatment of pain imposes an enormous burden on society, and is due, in part, to a limited understanding of biological events that underlie the transition from acute to chronic pain. Barriers to a better understanding of this transition have included an inability to selectively and efficiently visualize or manipulate specifc sensory neuron populations and the very low throughput of available methods to monitor nociceptor function at the cellular level. In this collaborative proposal, we have teamed together a developmental neurobiologist and several pain biologists to synergistically overcome both of these barriers. Using newly- developed molecular-genetic strategies, we will selectively label each of the four major subpopulations of low- threshold mechanoreceptive (LTMR) neurons, as well as peptidergic and MrgprD-expressing nonpeptidergic nociceptors, in mice. This technology will be combined with selective expression of the genetically encoded calcium indicator, GCAMP3, in mouse peripheral sensory neurons to permit direct visualization of neuronal activity in the skin and DRG. In our first two aims, these tools will allow us to efficiently and with high spatiotemporal resolution monitor changes in the anatomy and function of unambiguously defined nociceptor and LTMR populations during the development of neuropathic pain. These changes will be correlated with corresponding behavioral changes, monitored using classical and newly developed assays of thermal and mechanical sensitivity. In Aim 3, we will selectively ablate two LTMR populations that are candidate participants in pain and define their respective contributions to the establishment, maintenance, and manifestation of neuropathic mechanical hypersensitivity. Together, these studies will provide us with an unprecedented view of the dynamic processes associated with the transition to chronic pain and define cellular targets for the development of improved analgesic therapies.
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Agonist-evoked changes in TRPV ion channel selectivity
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财政年份:2007
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Agonist-evoked changes in TRPV ion channel selectivity
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依托单位:
海外基金