Neural circuit disruption by diffuse brain injury: basis for morbidity & therapy
Neural circuit disruption by diffuse brain injury: basis for morbidity & therapy
批准号:
8606663
负责人:
JONATHAN LIFSHITZ
金额:
$31.62万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-02-01 至 2016-01-31
关键词:
AcuteAddressAdultAgitationAnimal ModelAnti-Inflammatory AgentsAnti-inflammatoryAtrophicAttenuatedAxonBehaviorBehavioralBiological ModelsBlood VesselsBrainBrain InjuriesBrain regionCellular MembraneChronicCommunitiesDiffuseDiffuse Brain InjuryDoseFaceFigs - dietaryFreezingFunctional disorderGene ExpressionGoalsIbuprofenImmediate-Early GenesInflammationInflammatoryInjuryInterventionLeftLiquid substanceMeasuresMechanicsMedicalModelingMolecularMorbidity - disease rateNatureNeurodegenerative DisordersNeurologicNeurologic DysfunctionsNeuronal PlasticityNeuronsPathologic ProcessesPercussionPerformancePharmaceutical PreparationsProcessQuality of lifeRattusRegimenRehabilitation therapyResearchResolutionRodentSensorySeveritiesSocietiesSomatosensory CortexSurvivorsSymptomsTestingTherapeuticTimeTraumatic Brain InjuryVentral Posterior NucleusVibrissaebaseclinically relevanteffective therapyexperienceimprovedin vivo ModelinjuredinnovationmRNA Expressionmalemanneural circuitneuroinflammationneuropathologynovelorganic basepreventprotein expressionpsychologicpublic health relevanceresponsesomatosensorytooltreatment strategy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Our long term goals are to develop effective pharmacological and rehabilitative treatment strategies that promote adaptive reorganization of brain-injured circuits to mitigate neurological dysfunction (morbidity) after diffuse traumatic brain injury (TBI). To achieve these goals, we will exploit a novel, reproducible, late-onset neurological deficit that we have observed in the diffuse brain-injured rat, analogous to agitation in brain injury survivors. In contrast to the soothing and pacifying nature of facial whisker stimulation in uninjured rats, brain- injured rats react to whisker stimulation by cowering, freezing and guarding the mystacial pads. This aberrant behavior is concomitant with axonal damage, neuronal atrophy, persistent inflammation and neuroplasticity, such that whisker stimulation activates brain regions outside the conventional somatosensory whisker circuit. The current proposal tests the hypothesis that diffuse brain injury-induced inflammation drives the maladaptive structural plasticity responsible for aberrant behavioral responses to whisker stimulation. The model system afforded by the brain-injured somatosensory whisker circuit provides a reductionistic approach to the complexity of diffuse TBI, to address pathological and reparative mechanisms associated with post-traumatic morbidity. This circuit in diffuse brain-injured adult male rats will be evaluated for (Aim 1) aberrant behaviors elicited by whisker stimulation, (Aim 2) chronic neuropathology, neuronal activation and circuit reorganization, and (Aim 3) neuroinflammation-driven neuroplastic responses that contribute to circuit reorganization and morbidity. An anti-inflammatory therapeutic regimen may provide a clinically relevant intervention to prevent circuit rewiring and the onset of morbidity. The innovative combination of behavioral, anatomical, functional and therapeutic approaches directed at the brain-injured somatosensory whisker circuit addresses the underlying mechanisms associated with unregulated structural plasticity in the injured brain. Uncovering these processes can direct treatments to mitigate the onset, reduce the duration and/or promote the resolution of neurological dysfunction. Results from this circuit can ultimately be expanded to other circuits in rodents and then man to improve quality of life for millions of TBI survivors and potentially others suffering from progressive neurodegenerative diseases.
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DOI:
10.3109/02699052.2014.888768
发表时间:
2014
期刊:
Brain injury
影响因子:
1.9
作者:
[Rowe RK, Harrison JL, O'Hara BF, Lifshitz J]
通讯作者:
Lifshitz J
DOI:
10.1016/j.bbr.2016.12.038
发表时间:
2018-03-15
期刊:
Behavioural brain research
影响因子:
2.7
作者:
[Thomas TC, Ogle SB, Rumney BM, May HG, Adelson PD, Lifshitz J]
通讯作者:
Lifshitz J
DOI:
10.1016/j.neuroscience.2017.07.027
发表时间:
2017-09-17
期刊:
Neuroscience
影响因子:
3.3
作者:
[Ziebell JM, Ray-Jones H, Lifshitz J]
通讯作者:
Lifshitz J
Experimental diffuse brain injury results in regional alteration of gross vascular morphology independent of neuropathology.
实验性弥漫性脑损伤导致大血管形态的区域改变,与神经病理学无关。
DOI:
10.3109/02699052.2015.1090012
发表时间:
2016
期刊:
Brain injury
影响因子:
1.9
作者:
[Ziebell,JennaM, Rowe,RachelK, Harrison,JordanL, Eakin,KatharineC, Colburn,Taylor, Willyerd,FAnthony, Lifshitz,Jonathan]
通讯作者:
Lifshitz,Jonathan
The time course of activity-regulated cytoskeletal (ARC) gene and protein expression in the whisker-barrel circuit using two paradigms of whisker stimulation.
使用两个晶须刺激范式在晶须桶回路中,活性调节的细胞骨架(ARC)基因和蛋白表达的时间过程。
DOI:
10.1016/j.bbr.2015.01.032
发表时间:
2015-05-01
期刊:
Behavioural brain research
影响因子:
2.7
作者:
[Khodadad A, Adelson PD, Lifshitz J, Thomas TC]
通讯作者:
Thomas TC
共 14 条
Molecular Tool Development to Identify, Isolate, and Interrogate the Rod Microglia Phenotype in Neurological Disease and Injury
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批准号:10599762
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财政年份:2023
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Miniscope in vivo imaging of cumulative traumatic brain injury
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Miniscope in vivo imaging of cumulative traumatic brain injury
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Gravida traumatic brain injury (TBI) impacts neurodevelopment of the offspring
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财政年份:2023
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Mechanistic role of vascular dysfunction in TBI-mediated cognitive dysfunction
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批准号:10610367
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资助金额:$0.0万
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财政年份:2021
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负责人:JONATHAN LIFSHITZ
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Mechanistic role of vascular dysfunction in TBI-mediated cognitive dysfunction
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批准号:10188260
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资助金额:$0.0万
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财政年份:2021
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Mechanistic role of vascular dysfunction in TBI-mediated cognitive dysfunction
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批准号:10391335
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资助金额:$0.0万
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财政年份:2021
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负责人:JONATHAN LIFSHITZ
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依托单位:
Brain injury rehabilitation modality, regulation, & structural plasticity
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批准号:9763360
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项目类别:
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资助金额:$0.0万
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财政年份:2018
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负责人:JONATHAN LIFSHITZ
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依托单位:
Brain injury rehabilitation modality, regulation, & structural plasticity
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批准号:10226791
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项目类别:
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资助金额:$0.0万
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财政年份:2018
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负责人:JONATHAN LIFSHITZ
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依托单位:
Brain injury rehabilitation modality, regulation, & structural plasticity
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批准号:10454815
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项目类别:
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资助金额:$0.0万
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财政年份:2018
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负责人:JONATHAN LIFSHITZ
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依托单位:
Brain injury rehabilitation modality, regulation, & structural plasticity
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批准号:10670067
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项目类别:
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资助金额:$0.0万
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财政年份:2018
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负责人:JONATHAN LIFSHITZ
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依托单位:
Brain injury rehabilitation modality, regulation, & structural plasticity
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批准号:10011596
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项目类别:
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资助金额:$0.0万
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财政年份:2018
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负责人:JONATHAN LIFSHITZ
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依托单位:
Remote ischemic conditioning mitigates diffuse traumatic brain injury via specialized pro-resolving mediators
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批准号:9250598
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项目类别:
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资助金额:$25.26万
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财政年份:2016
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负责人:JONATHAN LIFSHITZ
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依托单位:
Investigating the role of lysophosphatidic acid (LPA) in pediatric brain injury
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批准号:9066824
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财政年份:2015
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负责人:JONATHAN LIFSHITZ
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依托单位:
Inhibition of synaptogenesis mitigates late-onset post-traumatic morbidity in rat
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批准号:8541899
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资助金额:$7.31万
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财政年份:2012
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负责人:JONATHAN LIFSHITZ
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依托单位:
Inhibition of synaptogenesis mitigates late-onset post-traumatic morbidity in rat
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批准号:8298806
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资助金额:$7.58万
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财政年份:2012
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负责人:JONATHAN LIFSHITZ
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Post Traumatic Sleep: An Individualized Indicator of Severity and Recovery
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资助金额:$21.81万
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负责人:JONATHAN LIFSHITZ
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依托单位:
Post Traumatic Sleep: An Individualized Indicator of Severity and Recovery
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批准号:8263023
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项目类别:
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资助金额:$18.94万
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财政年份:2011
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负责人:JONATHAN LIFSHITZ
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依托单位:
Neural circuit disruption by diffuse brain injury: basis for morbidity & therapy
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批准号:8537061
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项目类别:
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资助金额:$24.61万
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财政年份:2010
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负责人:JONATHAN LIFSHITZ
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依托单位:
Neural circuit disruption by diffuse brain injury: basis for morbidity & therapy
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批准号:8119912
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项目类别:
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资助金额:$3.21万
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财政年份:2010
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负责人:JONATHAN LIFSHITZ
-
依托单位:
海外基金