Mechanisms of Stress-Induced Pain in Veterans
Mechanisms of Stress-Induced Pain in Veterans
批准号:
9898305
负责人:
Anthony Christopher Johnson
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-04-01 至 2022-03-31
关键词:
AddressAfghanistanAmygdaloid structureAnimal ModelAnimalsAnxietyAreaAxonBehaviorBrainBrain regionCannulasCaringCell NucleusChronic stressClinicalComplexConsciousCorticosteroneCorticotropin-Releasing HormoneCorticotropin-Releasing Hormone ReceptorsDevelopmentElectrophysiology (science)EnsureExposure toFreedomFutureGlutamatesGoalsGrantHealthHealth systemHealthcareHormonesHyperalgesiaHypersensitivityIn VitroInternationalIraqJournalsK-Series Research Career ProgramsKnowledgeLaboratoriesLasersLeadLifeMeasuresMedialMental DepressionMentorsMentorshipMethodsMissionModelingMolecularMolecular TargetNeuronsNeurosecretory SystemsNeurotransmittersNociceptionOperative Surgical ProceduresOpsinOutcomes ResearchPainPathway interactionsPatient CarePersistent painPharmaceutical PreparationsPharmacologyPopulationPost-Traumatic Stress DisordersPrefrontal CortexPublishingQuality of lifeRattusRegulationResearchRiskRoleScientistSignal TransductionStatistical Data InterpretationStressStructureStructure of terminal stria nuclei of preoptic regionSynapsesTechniquesTestingTherapeuticTimeTrainingVeteransVisceralVisceral painbehavioral pharmacologybehavioral studybiological adaptation to stressbrain circuitrybrain dysfunctioncareercareer developmentchronic paincomorbid depressioncomorbiditydesigneffective therapyexperienceexperimental studyhealth dataimaging studyimplantationimprovedin vivoknock-downmeetingsnew therapeutic targetnovelnovel therapeuticsoperationoptogeneticsoral communicationpain behaviorpain inhibitionpain perceptionreceptorresponseresponsible research conductskillstool
中文摘要
伊拉克自由行动/持久自由行动/新黎明行动(OIF/OEF/OND)
英文摘要
Many Operation Iraqi Freedom/Operation Enduring Freedom/Operation New Dawn (OIF/OEF/OND)
veterans experience chronic pain, which is worsened by co-morbid conditions such as post-traumatic stress
disorder (PTSD) and depression. Significantly, there is an unmet clinical need to provide effective treatments
for chronic pain. One hurdle for the development of new therapies is a lack of understanding which
neurotransmitters and brain circuits are responsible for the persistence of chronic pain. Thus, this career
development application will provide the necessary training to develop an independent VA scientist capable of
researching novel brain circuitry responsible for the development of stress-induced chronic pain.
OBJECTIVES: The objective of this study is to identify the brain circuitry responsible for persistent stress-
induced pain and comorbid behaviors using targeted brain manipulations, including optogenetic techniques.
The overarching hypothesis is that stress induces imbalanced signaling within the limbic brain circuitry
to produce persistent pain hypersensitivity.
RESEARCH PLAN: This project will utilize two interrelated, independent specific aims. Specific Aim 1 will
test the hypothesis that stress-induced increases corticotropin-releasing factor signaling in the medial
prefrontal cortex leads to persistent visceral and somatic pain-like behaviors. Specific Aim 2 will test the
hypothesis that an imbalance in signaling between limbic brain regions, regulated by corticotropin-releasing
factor and glutamatergic receptors, is responsible for chronic stress-induced hypersensitivity. We will use a
combination of targeted stereotaxic surgeries, cannula implantations, drug microinfusions, and laser
stimulation to modify nociceptive, anxiety-like, and depression-like behaviors in conscious, freely moving rats.
TRAINING PLAN: Through his mentoring team and consultants, the candidate will receive training on how
to conduct the optogenetic, electrophysiological, and behavioral studies needed to address the research plan.
Additionally, the candidate will take formal courses to promote his professional development, including
responsible conduct of research, statistical analysis, and laboratory management. With formal mentorship to
improve his written and oral communication, the candidate will be able to present the findings of this research
at national and international meetings and publish the results in quality journals.
ANTICIPATED OUTCOMES: The research in Aim 1 will demonstrate that stress-induces increases in
corticotropin-releasing factor expression within the medial prefrontal cortex leading to enhanced visceral and
somatic sensitivity, which signals through corticotropin-releasing factor receptors in the bed nucleus of the stria
terminalis to produce the behaviors. Specific Aim 2 will show using optogenetic activation that activation of
amygdala terminals or inhibition of medial prefrontal cortex terminals in the bed nucleus of the stria terminalis
will produce visceral and somatic hypersensitivity in non-stressed rats. The experiments will also demonstrate
that inhibiting amygdala signaling (corticotropin-releasing factor) while stimulating medial prefrontal cortex
signaling (glutamate) in chronically stressed rats will inhibit pain-like behaviors. Completion of these Specific
Aims, along with the proposed mentoring and training, will ensure that the candidate develops his research
skills to submit a future VA Merit grant and eventually becomes a life-long VA Research Career Scientist.
SIGNIFICANCE TO VETERANS HEALTH: Scientifically, the results from this project will identify a novel
stress-associated brain circuit, along with the specific neurotransmitters, that modulates chronic pain.
Identification of the mechanisms and circuitry involved in chronic stress-induced pain could lead to new targets
for therapies to treat veterans experiencing chronic pain, which is a significant unmet healthcare burden.
Professionally, this career development award will produce an independent scientist with the capability of
investigating chronic pain mechanisms to provide additional tools to improve the quality-of-life for veterans.
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会议论文
Amygdala Mediated Mechanisms Regulating Visceral Pain
-
批准号:10320942
-
项目类别:
-
资助金额:$32.63万
-
财政年份:2020
-
负责人:Anthony Christopher Johnson
-
依托单位:
Amygdala Mediated Mechanisms Regulating Visceral Pain
-
批准号:10549783
-
项目类别:
-
资助金额:$32.63万
-
财政年份:2020
-
负责人:Anthony Christopher Johnson
-
依托单位:
Amygdala Mediated Mechanisms Regulating Visceral Pain
-
批准号:10078267
-
项目类别:
-
资助金额:$32.63万
-
财政年份:2020
-
负责人:Anthony Christopher Johnson
-
依托单位:
Mechanisms of Stress-Induced Pain in Veterans
-
批准号:10158407
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2017
-
负责人:Anthony Christopher Johnson
-
依托单位:
Central Molecular Mechanisms of Stress-Induced Visceral Hypersensitivity
-
批准号:8197975
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项目类别:
-
资助金额:$2.58万
-
财政年份:2010
-
负责人:Anthony Christopher Johnson
-
依托单位:
Central Molecular Mechanisms of Stress-Induced Visceral Hypersensitivity
-
批准号:8005669
-
项目类别:
-
资助金额:$2.54万
-
财政年份:2010
-
负责人:Anthony Christopher Johnson
-
依托单位:
Central Molecular Mechanisms of Stress-Induced Visceral Hypersensitivity
-
批准号:8329013
-
项目类别:
-
资助金额:$2.62万
-
财政年份:2010
-
负责人:Anthony Christopher Johnson
-
依托单位:
海外基金