grant

Posterior Hypothalamic Contribution to Stress Adaptation

Organization UNIVERSITY OF COLORADOLocation Boulder, UNITED STATESPosted 17 Apr 2024Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY20254-Aminobutanoic Acid4-Aminobutyric Acid4-amino-butanoic acidAffectAffectiveAffective DisordersAminalonAminaloneAmygdalaAmygdaloid BodyAmygdaloid NucleusAmygdaloid structureAnatomic SitesAnatomic structuresAnatomyAnxiety DisordersBehavioralBrainBrain Nervous SystemBrain regionCalciumCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemCatecholaminesCausalityCell BodyCell Communication and SignalingCell NucleusCell SignalingCellsChronic stressClinicalCognitiveCommon Rat StrainsComplexDREADDsDecision MakingDevelopmentDifferences between sexesDiffers between sexesDiseaseDisorderElementsEmotionalEncephalonEtiologyExposure toFemaleFiberFore-BrainForebrainGABAGenderGene TranscriptionGeneticGenetic TechnicsGenetic TechniquesGenetic TranscriptionGlucocorticoidsGlutamatesHeart VascularHumanHypothalamic structureHypothalamusImpairmentIncidenceIndividualIntracellular Communication and SignalingL-GlutamateLaboratoriesLeadLimbic SystemMediatingMemoryMethodsModalityModern ManModificationMood DisordersMoodsNerve Transmitter SubstancesNeuroendocrineNeuroendocrine SystemNeurosecretory SystemsNeurotransmittersNodalNucleusOrganismParaventricular Nucleus of ThalamusParaventricular Thalamic NucleusPb elementPhotometryPhysiologicPhysiologicalPopulationPositionPositioning AttributePosterior Hypothalamic RegionPosterior HypothalamusPrecipitationPrevalenceProcessProsencephalonPsychopathologyRNA ExpressionRatRats MammalsRattusReactionRecurrenceRecurrentRegulationReportingRiskRoleSensorySex DifferencesSexual differencesSignal TransductionSignal Transduction SystemsSignalingSourceSpecific qualifier valueSpecificitySpecifiedStressStructure of paraventricular nucleus of thalamusSympathinsSystemTechniquesTestingTranscriptionTranscriptional ControlTranscriptional RegulationViralabnormal psychologyamygdaloid nuclear complexbehavior responsebehavioral responsebiological adaptation to stressbiological signal transductioncausationcirculatory systemcognitive functioncopingdesigndesigner receptors exclusively activated by designer drugsdesigningdevelopmentaldisease causationexperiencegamma-Aminobutyric Acidglutamatergichabituationheavy metal Pbheavy metal leadhypothalamicindexinginnervationliving systemmalenerve supplyneuralneural adaptationneural circuitneural circuitryneural mechanismneuroadaptationneurocircuitryneuromechanismnew drug treatmentsnew drugsnew pharmacological therapeuticnew therapeuticsnew therapynext generation therapeuticsnovelnovel drug treatmentsnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel therapeuticsnovel therapypostsynapticprecipitationspresynapticpromoterpromotorpsychologicpsychologicalreaction; crisisresponsesensorsexsex based differencessex-dependent differencessex-related differencessex-specific differencessocial rolestress reductionstress responsestress; reactionstressorsynaptic circuitsynaptic circuitryγ-Aminobutyric Acid
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

Project Summary
The overall aim of this project is to determine the contribution of the rostral region of the posterior hypothalamic

nucleus (rPH) in stress adaptation. More specifically, stress habituation is defined as a progressive reduction in

responses upon repeated exposures to the same (homotypic) stressor. Psychological or “emotional” stressors

elicit a range of behavioral, autonomic, and neuroendocrine responses that normally help organisms cope with

perceived or actual threatening situations. However, prolonged, unabated and chronic stress exposure is

frequently associated with the development, precipitation, or exacerbation of several psychopathologies and

physical disorders. The sustained activation of stress responsive systems can negatively affect physiologic

functions and ultimately, survival. Thus, the reduction or inhibition of stress-elicited responses afforded by

habituation is likely a vital mechanism serving to reduce the cumulative impact of the same stressors experienced

repeatedly. Importantly, impaired habituation has been reported in several human clinical populations including

anxiety and mood disorders. Unfortunately, the neural mechanisms responsible for stress habituation are still ill-

defined, which makes it currently impossible to evaluate the contribution of habituation in psychopathologies.

In this application, robust habituated neuroendocrine, autonomic and behavioral responses will be obtained

to repeated homotypic stress paradigms that will test the response specificity and generality of the proposed

brain manipulations. Based on detailed anatomical and functional results from our laboratory, emphasis will be

placed on the role of the rPH in the acquisition of stress habituation. Anatomically, the rPH is located at a focal

intersection between several sensory, limbic forebrain, and effector response systems activated by various

stressors, placing it in a unique position to undergo habituation-related plasticity that can regulate coordinated

responses to stress. The first aim is therefore directed at evaluating the novel hypothesis that the rPH region,

and some of its specific cell populations, contribute to the acquisition of stress habituation. Aim 2 seeks to

evaluate the possibility that intrinsic rPH neural activity is modified by repeated homotypic stress. Throughout

these aims, both female and male rats will be evaluated for putative rPH-related differences in stress adaptation

due to the differential prevalence of gender to anxiety and mood disorders and the widely reported sex

differences in habituation to stress. The proposed anatomical, functional and behavioral analyses of the rPH in

stress adaptation through habituation is novel and will provide converging evidence implicating this brain region

in stress adaptation and its sequelae.

Grant Number: 5R21MH133108-02
NIH Institute/Center: NIH

Principal Investigator: SERGE CAMPEAU

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →