grant

Elucidating the role for MCH neurons in feeding behavior and responses to sensory food cues

Organization UNIVERSITY OF MICHIGAN AT ANN ARBORLocation ANN ARBOR, UNITED STATESPosted 15 Aug 2021Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2025Adaptive BehaviorsAdvertisementAdvertisementsAmygdalaAmygdaloid BodyAmygdaloid NucleusAmygdaloid structureAnatomic SitesAnatomic structuresAnatomyAnorexiaArcuate NucleusAreaArousalAttentionAutomobile DrivingBasic ResearchBasic ScienceBehaviorBehavioralBrainBrain Nervous SystemBrain regionCandyCell Communication and SignalingCell SignalingCognitiveConfectionConsummatory BehaviorConsumptionCuesEatingEating DisordersEncephalonEnvironmentFeeding behaviorsFiberFinancial costFoodFood IntakeFood ProcessingFosteringFutureGeneticGoalsHealthHealth Care CostsHealth CostsHumanHungerHyperphagiaHypothalamic structureHypothalamusIn vivo two-photon calcium imagingInfundibular NucleusIngestive BehaviorInjectionsIntermediary MetabolismIntracellular Communication and SignalingInvestigationKO miceKnock-out MiceKnockout MiceLateralLearningMCH receptorMapsMediatingMetabolicMetabolic ProcessesMetabolismMissionModelingModern ManModernizationNational Institutes of HealthNerve CellsNerve UnitNeural CellNeurocyteNeuronsNucleus AccumbensNull MouseObesityObesity EpidemicOvereatingPathway interactionsPeptide Hormone GenePhenotypePhotometryPopulationPrevalenceProcessPublic HealthRabies mappingRabies trans synaptic tracingRabies virus mediated mappingResearchRewardsRoleSensorySignal TransductionSignal Transduction SystemsSignalingSiteSleepSocietiesStimulusStructureStructure of nucleus infundibularis hypothalamiSystemUnited States National Institutes of HealthVisualWorkadaptation behavioradaptive behavioradiposityamygdaloid nuclear complexbehavior responsebehavioral responsebillboardbiological signal transductioncorpulencecravingdrivingeating cuesfeedingfeeding-related behaviorsfood Ingestionfood consumptionfood cueshormonal signalshormone signalshunger cueshypothalamicimaging approachimaging based approachimprovedin vivoin vivo calcium imaginginnovateinnovationinnovativemelanin-concentrating hormonemelanin-concentrating hormone receptormelanine-concentrating hormone receptormelanophore-concentrating hormonemelanosome concentrating hormonemonetary costneuralneural mechanismneuromechanismneuronalnutrient intake activityoptogeneticspathwaypeptide hormoneperceptual stimulusphysicochemical phenomena related to the sensespolyphagiarabies based mappingrabies based retrograde mappingrabies circuit tracingrabies mediated retrograde monosynaptic tracingrabies retrograde tracingrabies tracerrabies tracingrabies viral tracingrabies virus mediated circuit mappingrabies virus monosynaptic circuit tracingrabies virus monosynaptic tracingrabies virus neurotracerrabies virus retrograde tracingrabies virus tracingresponsereward processingsensory stimulussleep behaviorsleep habitsleep/wake behaviorsocial roletooltracing with rabieszona incerta
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Full Description

Project summary
America has an obesity epidemic, which is getting progressively worse and has immense human and

financial costs. While our understanding of homeostatic feeding circuits has advanced steadily over the past

several decades much remains unclear. In addition, much of our food consumption is not due to homeostatic

need, instead, it is often a result of non-homeostatic drivers. Cravings for sugary or fatty foods, even when

sated, drive increased consumption. Stimuli in our environment that signal food availability, including food-

associated visual cues in the form of advertisements, billboards, and candy-bar wrappers, promote these

cravings, and, ultimately, promote consumption. We aim to understand the circuits that drive feeding behavior,

including how food-associated sensory stimuli can hijack normally advantageous neural processes to increase

consumption and contribute to the obesity epidemic.

We propose to determine the role of melanin-concentrating hormone (MCH) neurons in regulating

feeding and responses to food-associated cues. MCH neurons in the lateral hypothalamus and zona incerta

project throughout the brain, including to limbic and higher-order brain regions, and can drive a diverse array of

behaviors, such as feeding, sleep, and learning. Discrete MCH subpopulations likely serve separate functions;

for example, some might promote feeding while others promote sleep or other consummatory behaviors. Our

central hypothesis is that MCH neurons will drive food consumption, increase the rewarding value of

consummatory behavior and enhance responses to food-associated cues through projections to the arcuate

nucleus, nucleus accumbens, and basolateral amygdala.

We will first identify the activity and projection profiles of MCH neuron subpopulations that drive feeding

by mapping specific subpopulations of MCH neurons and recording their activity across a range of feeding

behaviors. We will then activate specific MCH projections to determine if they are capable of driving feeding

behaviors, in addition to other MCH-related behaviors, including sleep. We expect that a specific subpopulation

of MCH neurons projecting to the nucleus accumbens and basolateral amygdala will respond to food rewards

and increase consummatory behaviors. Finally, we will use in vivo two-photon calcium imaging to investigate

the role for MCH activity in forming enhanced behavioral and sensory responses to food-associated cues. By

using cutting-edge tools and approaches to identify the role for the MCH system in feeding behavior and

responses to food cues, we will generate findings that can help to identify cognitive targets and mechanisms

for treating maladaptive feeding behaviors.

Grant Number: 5R01DK129366-05
NIH Institute/Center: NIH

Principal Investigator: Christian Burgess

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