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Brain pathways in social evaluative threat

Brain pathways in social evaluative threat
社会评价威胁中的大脑通路
批准号:
8054597
负责人:
TOR D. WAGER
金额:
$19.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-02-26 至 2013-01-31
关键词:
AddressAffectAffectiveAmygdaloid structureAnimalsAnxietyAsthmaAttentionAutonomic PathwaysAutonomic nervous systemBasal GangliaBehavioral ResearchBrainBrain StemBrain imagingBrain regionCardiovascular DiseasesCardiovascular systemCell NucleusCerebrovascular CirculationChronicCognitionCognitiveCommunicationDataDevelopmentDiseaseDisease modelEmotionsEndocrineExpectancyFunctional Magnetic Resonance ImagingFundingFutureGenerationsGoalsHealthHeartHeart RateHumanHydrocortisoneHypothalamic structureImageImaging TechniquesImaging technologyImmuneImmunologic MarkersInfectionInsula of ReilInvestigationKnowledgeLaboratoriesLateralLinkLiteratureLungMagnetismMapsMeasuresMedialMediatingMental DepressionMethodsModelingMorphologic artifactsMultivariate AnalysisMydriasisNational Institute of Mental HealthNeuronsNeurosecretory SystemsOutputPainPaperParoxysmal DyspneaParticipantPathway interactionsPerfusionPeripheralPhysiologicalPhysiologyPopulationPredispositionPrefrontal CortexRecoveryResearchResolutionSafetySample SizeServicesSignal TransductionSocial statusSpin LabelsStressStructureSystemTechniquesTechnologyTestingTimeTissuesTranslatingTrier Social Stress TestVariantVasomotorWorkWound Healingadverse outcomebasal forebrainbasebrain pathwaychemokinecytokineforginghypothalamic-pituitary-adrenal axisimaging modalityimmune functionimprovedinsightinterestlocus ceruleus structuremidbrain central gray substanceneuroimagingnovelpsychologicpublic health relevanceresearch studyresponsesocialstressortool

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DESCRIPTION (provided by applicant): Several new developments in neuroimaging techniques have paved the way for advances in understanding cortical-brainstem-autonomic and cortical-hypothalamic-endocrine pathways. Advances come from both acquisition techniques, including the development of spin-echo continuous arterial spin labeling (SE-CASL) fMRI, and improvements in analysis tools, including the development of multi-level path models capable of localizing and making population inference on brain pathways. In this project, the novel combination of these two techniques will be used to accomplish two aims: First, to identify cortical-brainstem and cortical- hypothalamic pathways mediating peripheral responses to social evaluative threat (Aim 1), and second, to examine modulation of functional threat-pathway strength by the prefrontal cortex (Aim 2). The ability to identify brain pathways involved in threat is important because a large literature in animals and humans suggests that psychological threat and `stress' are potentially linked to adverse outcomes in many diseases, including cardiovascular health, asthma, wound healing and immune function, depression, and others. But there is a critical gap in knowledge about the specific brain mechanisms that link psychological threat to peripheral activity in humans. Questions about brain mechanisms of emotion and questions about endocrine and autonomic physiology have largely been addressed by separate studies in separate fields. Using path analysis to examine both CASL-fMRI and peripheral responses (cortisol and basic measures of autonomic output) will allow us to forge links between `higher cortical' brain activity, subcortical centers in hypothalamus and brainstem, and peripheral responses. Identifying brain pathways is a new endeavor, as most fMRI studies examine regional brain activation, either ignoring how brain regions are connected or analyzing simple measures of connectivity between two regions. Path analysis can be used to identify pathways that span multiple regions and measures, providing potential for new insights into human brain-peripheral communication. SE-CASL was selected as a technique because it is particularly suited to studying the hypothalamus and brainstem, with improved spatial localization, more reliable signal and reduced artifacts around these regions, and stability over time, making it suitable for examining sustained brain and physiological responses to social evaluative threat. PUBLIC HEALTH RELEVANCE: Threats to both physical safety and social status produce marked autonomic and neuroendocrine responses in humans, and chronic physiological threat responses are associated with a number of disorders, including depression, anxiety, cardiovascular disease, infection, and others. Though threat responses have been carefully studied in nonhuman animals, little is known about the specific cortical-brainstem-body pathways that translate uniquely human cognitions about the social situation into physiological responses. This project combines advanced multivariate analysis techniques with cutting-edge methods for imaging the brainstem to map these pathways, providing insight into how threat responses are generated and regulated in the human brain.
期刊论文(3)
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会议论文
DOI: 10.1155/2012/818456
发表时间: 2012
期刊: International journal of biomedical imaging
影响因子: 7.6
作者: [Borogovac A, Asllani I]
通讯作者: Asllani I
DOI: 10.1016/j.neuroimage.2012.03.070
发表时间: 2012-07-16
期刊: NEUROIMAGE
影响因子: 5.7
作者: [Cribben, Ivor, Haraldsdottir, Ragnheidur, Atlas, Lauren Y., Wager, Tor D., Lindquist, Martin A.]
通讯作者: Lindquist, Martin A.
Psychosocial risk factors for chronic pain: Characterizing brain and genetic pathways and variation across understudied populations
  • 批准号:
    10599396
  • 项目类别:
  • 资助金额:
    $45.88万
  • 财政年份:
    2022
  • 负责人:
    TOR D. WAGER
  • 依托单位:
The neural bases of placebo effects and their relation to regulatory processes
  • 批准号:
    10358505
  • 项目类别:
  • 资助金额:
    $71.46万
  • 财政年份:
    2019
  • 负责人:
    TOR D. WAGER
  • 依托单位:
The neural bases of placebo effects and their relation to regulatory processes
  • 批准号:
    10056222
  • 项目类别:
  • 资助金额:
    $74.06万
  • 财政年份:
    2019
  • 负责人:
    TOR D. WAGER
  • 依托单位:
The neural bases of placebo effects and their relation to regulatory processes
  • 批准号:
    10539287
  • 项目类别:
  • 资助金额:
    $70.06万
  • 财政年份:
    2019
  • 负责人:
    TOR D. WAGER
  • 依托单位:
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