grant

Unmasking neuromodulatory control of locomotion

Organization WASHINGTON UNIVERSITYLocation SAINT LOUIS, UNITED STATESPosted 16 Aug 2024Deadline 31 May 2027
NIHUS FederalResearch GrantFY20255-HT5-HT Receptors5-Hydroxytryptamine5-Hydroxytryptamine Receptors5HTActive Follow-upAcuteAffectAgeAgonistAnimalsAxonAxotomyBathingBathsBehaviorBehavioralBrachydanio rerioBrainBrain Nervous SystemCell BodyCell Communication and SignalingCell FunctionCell PhysiologyCell ProcessCell SignalingCellsCellular FunctionCellular PhysiologyCellular ProcessComputer ModelsComputerized ModelsConflictConflict (Psychology)Connector NeuronCyclicityDanio rerioDataDevelopmentDopamineDopamine ReceptorDrugsElectrophysiologyElectrophysiology (science)EncephalonEnteramineExhibitsFrequenciesFutureGeneticHeadHippophaineHydroxytyramineHypothalamic structureHypothalamusImageImaging DeviceImaging InstrumentImaging ToolIntercalary NeuronIntercalated NeuronsInterneuronsInternuncial CellInternuncial NeuronIntracellular Communication and SignalingLocomotionLocomotor ActivityMeasuresMedicationMedulla SpinalisModelingMotorMotor ActivityMotor CellMotor NeuronsMotor outputMovementNerve CellsNerve UnitNeural CellNeurocyteNeuromodulatorNeuronsNeurophysiology / ElectrophysiologyNormal RangeNormal ValuesOutputPathway interactionsPerformancePeriodicityPharmaceutical PreparationsPharmacologyPopulationPreparationPropertyReceptor ProteinReporterRhythmicitySeriesSerotoninSignal TransductionSignal Transduction SystemsSignalingSpeedSpinalSpinal CordStimulusSubcellular ProcessSwimmingSynapsesSynapticSystemTestingTimeVariantVariationVertebrate AnimalsVertebratesVisualWorkZebra DanioZebra FishZebrafishactive followupagesantagonismantagonistbasebasesbehavior influencebehavioral influencebiological signal transductionbody movementcomputational modelingcomputational modelscomputer based modelscomputer based predictioncomputerized modelingdevelopmentaldrug/agentelectrophysiologicalexperimentexperimental researchexperimental studyexperimentsfollow upfollow-upfollowed upfollowupgenetic approachgenetic strategyhypothalamicimagingin vivomotoneuronmotor behaviormotor controlneural controlneural regulationneuromodulationneuromodulatoryneuronalneuroregulationpathwaypharmacologicpostsynapticpredictive modelingpreparationsreceptorrecruitrestraintsensorserotonin receptorspatial and temporalspatial temporalspatiotemporalsynapsetoolvertebrata
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
Neuromodulators including dopamine and serotonin have profound effects on spinal circuits for locomotion. A wealth

of pharmacological manipulations has shown that drugs mimicking or blocking these neuromodulators can change the

properties of rhythmic motor output in the isolated spinal cord. However, these studies often conflict and cannot

capture the normal range of behaviors expressed in vivo. Furthermore, it is entirely unknown whether neuromodulators

are released onto different spinal targets across different behaviors. Finally, neuromodulatory neurons are highly

branched, making it difficult to disambiguate the spinal vs supraspinal consequences of their action. We will leverage

new tools for imaging and manipulating neuromodulator signaling, combined with the transparency and accessibility of

the young zebrafish, and a quantitative modeling approach, to understand the effects of dopamine and serotonin on

genetically defined components of the spinal locomotor circuit in vivo. First, we will measure the activity of

neuromodulatory axons during three distinct behaviors, testing whether dopamine and serotonin axons differentially

participate in these behaviors. Next, we will quantify neuromodulator release during these behaviors directly, both in

the whole spinal cord and in genetically defined populations of neurons with distinct contributions to locomotion. We

will then test the significance of descending neuromodulatory influence on spinal circuits by targeted axotomy that will

allow disambiguation of the spinal and supraspinal consequences of neuromodulator release. Finally, using newly

developed chemogenetic approaches, we will selectively block neuromodulatory receptors in motor neurons and

measure the consequences on the three distinct behaviors in freely moving animals. Throughout the project, we will

use experimental data to develop both single-segment and multi-segment computational models of neuromodulatory

action, and in turn use these models to make testable predictions about circuits and behavior. Together, these

experiments will reveal for the first time when and where dopamine and serotonin are acting in the spinal locomotor

circuit, and how their actions influence behavior in vivo.

Grant Number: 5U01NS136458-02
NIH Institute/Center: NIH

Principal Investigator: Martha Bagnall

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 →