grant

Plasticity of cortical networks during learning

Organization YALE UNIVERSITYLocation NEW HAVEN, UNITED STATESPosted 16 Sept 2022Deadline 15 Sept 2026
NIHUS FederalResearch GrantFY20252-photonAbscissionAddressAnimalsAssociation LearningAssociative LearningAutomobile DrivingBehaviorBehavioralBehavioral ParadigmCalciumCuesDataDiseaseDisorderDorsalEventExcisionExhibitsExtirpationGoalsGraphHydrogen OxideImageImaging ProceduresImaging TechnicsImaging TechniquesIndividualLearningMethodsMotivationMotorMotor CortexNeocortexNerve CellsNerve UnitNeural CellNeurocyteNeuronsPavlovian conditioningPhasePopulationPrimary visual cortexProcessPyramidal neuronRemovalReversal LearningRewardsRoleSchizophreniaSchizophrenic DisordersShapesSiteStimulusStriate CortexStriate areaSurgical RemovalSymptomsTechniquesTestingTimeTrainingV1 neuronVisualWaterWorkaddictionaddictive disorderanalytical toolarea striataassociative conditioningclassical conditioningdementia praecoxdesigndesigningdrivingexperimentexperimental researchexperimental studyexperimentsfrontal cortexfrontal lobehippocampal pyramidal neuronhomotypical corteximagingimaging in miceimaging studies for miceimaging studies in miceinsightisocortexmice imagingmurine imagingneopalliumneuralneuronalnoveloptogeneticspreventpreventingrecruitresectionresponseschizophrenicsocial rolespatial and temporalspatial temporalspatiotemporaltwo-photonvisual cortical plasticityvisual plasticityvisual processvisual processing
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Full Description

PROJECT SUMMARY:
Plasticity occurs in the primary visual cortex (V1) in response to visual associative learning, where one

stimulus is paired with reward (CS+) and another is not (CS-). However, learning is not a unitary process, and

distinct stages of learning might drive contrasting plastic changes in V1. Indeed, previous work has found

dynamic changes in V1 pyramidal neuron activity and inputs at different times throughout learning. Experiments

separating distinct learning phases behaviorally are lacking, making it difficult to fully dissect V1 plasticity

changes throughout learning. To address this, we have designed a 3-phase associative learning task that

separates early, stimulus non-specific learning from late, stimulus-specific learning and reversal learning. We

will also manipulate stimulus value in two ways: devaluation and spout removal. Using this behavioral paradigm

along with 1- and 2-photon calcium imaging of the mouse dorsal cortex, we will test the following hypotheses: 1)

that visual associative learning differentially recruits V1 activity during distinct learning stages, 2) activity in V1 is

rapidly plastic in response to changes in stimulus value, 3) individual V1 neurons exhibit bidirectional plasticity

across learning, 4) visual associative learning changes cortico-cortical functional connectivity, and 5) V1 activity

is required to maintain these cortico-cortical functional connectivity changes. Our results will provide an

unprecedented level of insight into V1 plasticity throughout learning and stimulus value manipulation. We will,

for the first time, address how plasticity in V1 is mirrored across the dorsal cortex, or required for cortico-cortical

plasticity.

Grant Number: 3F30EY034380-03S1
NIH Institute/Center: NIH

Principal Investigator: Hannah Batchelor

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