Persisting functional CNS changes following peripheral nerve repair
周围神经修复后中枢神经系统功能持续变化
基本信息
- 批准号:9031926
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-01-01 至 2018-06-30
- 项目状态:已结题
- 来源:
- 关键词:AdultAfferent NeuronsAnatomyAnestheticsAnimalsAreaAttentionBehavioralBody RegionsBrainCentral Nervous System DiseasesClinicalCognitiveCommunicationCommunication impairmentDataDeafferentation procedureDiseaseElectric StimulationElectrophysiology (science)ElementsEsthesiaEventExcisionFaceFunctional Magnetic Resonance ImagingFundingFutureGoalsHealedImaging TechniquesImplanted ElectrodesInjuryLearningLesionLightLimb structureMagnetic Resonance ImagingMapsMeasuresModalityMonitorNerveNerve CrushNeuronsOperative Surgical ProceduresOutcomePathway interactionsPatientsPatternPerformancePeripheralPeripheral NervesPeripheral nerve injuryPhasePopulationProcessRattusRecoveryRehabilitation OutcomeRehabilitation therapyResearchRestSensorySeveritiesSignal TransductionSiteSourceStimulusTechniquesTechnologyTestingTherapeuticTimeVeteransWorkdesigndexteritydisabilityhealinghigh riskimaging biomarkerimaging modalityimprovedinjuredinjury and repairlongitudinal designnerve injurynerve transectionnovelnovel therapeutic interventionoperationoptogeneticsperipheral nerve transectionpreventpublic health relevancerepairedresearch studyresponsesensory cortexsensory inputsensory systemsuccesstraffickingviral gene deliveryvisual motor
项目摘要
DESCRIPTION (provided by applicant):
Peripheral nerve injury is a frequent source of disability and a particular challenge for rehabilitation in the Veteran population. Although techniques for surgical repair have progressed, outcomes remain unpredictable. In the past, connections of the periphery to the brain had been thought to be fixed in adults, but there is a growing recognition of plasticity in brain function associated with removal of peripheral sensory input. For instance, it is known that sensory cortex associated with denervated body regions become reassigned, and disordered cortical function persists after repair of a surgical lesion. However, successful use of the limbs requires not just brain connections to peripheral targets, but also the coordinated participation o numerous activities within the brain, including interaction with other sensory sites as well as motor, visual, and cognitive areas. We therefore hypothesize that disruption of interactive brain activity underlies rehabilitation challenges after nerve injury repair. New noninvasive technology now exists to assess the integrated performance of the brain. Specifically, functional magnetic resonance imaging (fMRI) can indicate coordinated activation of various brain loci, while resting state functional connectivity MRI (rs-fMRI) reveals patterns of communication between brain sites in the absence of stimuli. Our preliminary data show substantial disruption of coordinated brain function following experimental nerve injury and repair. We have the long-term goals of defining this phenomenon in temporal and anatomic detail, which would lay the groundwork for developing an imaging biomarker that could guide personalized rehabilitation that targets appropriate specific functions. We have the additional goal of testing whether artificially maintaining afferent sensory neuron activity to the brain during the healing phase after repair may lessen or prevent brain disorganization. In the work proposed in this SPiRE application, we will obtain initial observations to substantiate our hypotheses by defining brain responses to nerve injury/repair with and without supplying replacement afferent activity, in a limited number of animals in a longitudinal fashion, using our novel techniques. Further, we will develop the means to achieve neuronal stimulation for treatment of untethered animals using implantable optogenetic light sources that activate photosensitive channels expressed in sensory neurons after viral gene delivery. We believe that extending the rehabilitation perspective beyond the nerve repair to include brain function may open the door to a new level of refined rehabilitation assessment, planning, and success.
描述(由申请人提供):
周围神经损伤是导致残疾的常见原因,也是退伍军人康复的一个特殊挑战,尽管手术修复技术已经取得了进步,但结果仍然难以预测。在过去,周围神经与大脑的连接被认为是固定的。成人,但人们越来越认识到与去除外周感觉输入相关的大脑功能的可塑性,例如,众所周知,与去神经的身体区域相关的感觉皮层会被重新分配,并且在手术损伤修复后,紊乱的皮层功能仍然存在。然而,成功使用四肢不仅需要大脑与周围目标的连接,还需要大脑内众多活动的协调参与,包括与其他感觉部位以及运动、视觉和认知区域的相互作用,因此我们要努力克服这种干扰。交互式大脑活动是神经损伤修复后康复挑战的基础,现在有新的无创技术可以评估大脑的综合性能,具体来说,功能磁共振成像(fMRI)可以显示不同大脑位点的协调激活,而静息状态功能连接磁共振成像。 (rs-fMRI)揭示了之间的沟通模式我们的初步数据显示,实验性神经损伤和修复后,大脑的协调功能受到严重破坏,我们的长期目标是在时间和解剖细节上定义这种现象,这将为发展奠定基础。在本 SPiRE 提出的工作中,我们的另一个目标是测试在修复后的愈合阶段人工维持大脑的传入感觉神经元活动是否可以减轻或防止大脑紊乱。应用程序,我们将获得初步观察通过使用我们的新技术,在有限数量的动物中以纵向方式定义大脑对神经损伤/修复的反应(有或没有提供替代传入活动)来证实我们的假设。此外,我们将开发实现神经元刺激以治疗的方法。我们相信,将康复视角扩展到神经修复之外,包括脑功能,可能会为精细康复评估、规划、康复的新水平打开大门。和成功。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Quinn H Hogan其他文献
Selective RNAi-silencing of Schwann cell Piezo1 alleviates mechanical hypersensitization following peripheral nerve injury
雪旺细胞 Piezo1 的选择性 RNAi 沉默可减轻周围神经损伤后的机械过敏
- DOI:
10.21203/rs.3.rs-3405016/v1 - 发表时间:
2023-10-16 - 期刊:
- 影响因子:0
- 作者:
Br;on Itson;on;Uarda Gani;Ale;er R. Mikesell;er;Chengsheng Qiu;Fan Fan;Cheryl L Stucky;Quinn H Hogan;S. Shin;Hongwei Yu - 通讯作者:
Hongwei Yu
Quinn H Hogan的其他文献
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{{ truncateString('Quinn H Hogan', 18)}}的其他基金
Primary sensory neuron-targeted block of Cav3.2 for treatment of chronic neuropathic pain
初级感觉神经元靶向的 Cav3.2 阻断治疗慢性神经性疼痛
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10452646 - 财政年份:2021
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Primary sensory neuron-targeted block of Cav3.2 for treatment of chronic neuropathic pain
初级感觉神经元靶向的 Cav3.2 阻断治疗慢性神经性疼痛
- 批准号:
10438951 - 财政年份:2021
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Harnessing T-junction filtering; bidirectional control of sensory neuron impulse traffic
利用 T 形接头过滤;
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10200908 - 财政年份:2017
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-- - 项目类别:
Harnessing T-junction filtering; bidirectional control of sensory neuron impulse traffic
利用 T 形接头过滤;
- 批准号:
9419475 - 财政年份:2017
- 资助金额:
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Persisting functional CNS changes following peripheral nerve repair
周围神经修复后中枢神经系统功能持续变化
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9198176 - 财政年份:2016
- 资助金额:
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AAV-encoded analgesic peptide aptamers for chronic pain
AAV编码的镇痛肽适体治疗慢性疼痛
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9079673 - 财政年份:2016
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Cannabinoid Signaling in the dPAG: Specific Analgesic and Autonomic Functions
dPAG 中的大麻素信号传导:特定的镇痛和自主功能
- 批准号:
8966633 - 财政年份:2013
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Cannabinoid Signaling in the dPAG: Specific Analgesic and Autonomic Functions
dPAG 中的大麻素信号传导:特定的镇痛和自主功能
- 批准号:
8625117 - 财政年份:2013
- 资助金额:
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Cannabinoid Signaling in the dPAG: Specific Analgesic and Autonomic Functions
dPAG 中的大麻素信号传导:特定的镇痛和自主功能
- 批准号:
8762234 - 财政年份:2013
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DRG engraftment of transduced mesenchymal stem cells to treat neuropathic pain
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8463269 - 财政年份:2012
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