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ENCODING SALTATORY TACTILE VELOCITY IN THE HUMAN OROFACIAL
SOMATOSENSORY SYSTEM USING fMRI
Rebecca Custead, 1,3, Hyuntaek Oh 2,3, Steven M. Barlow 1-3
1Communication Disorders, 2Biological Systems Engineering, 3Center for Brain, Biology & Behavior, University of Nebraska, Lincoln, NE, USA
Processingdynamic tactileinputsisakeyfunctionofsomatosensorysystems.
Closelytiedtoskilled motoractivity, velocityencoding mechanismsare
importantforfinemotorcontrol(speech,swallow,etc.). Knowledgeof
sensoryprocessing networkscontributetoourunderstanding of
sensorimotorrecoveryfollowing neurologicalinsult.Todate,littleisknown
abouttactilevelocityencoding intrigeminalnetworksthatprocesscutaneous
afferentinformation associated withfacialsensation, proprioception, and
oromotorfeedback.
Background
Objective
Methods Results
Acknowledgements
Conclusions
References
Tousehighresolution fMRItoinvestigatetheneuralsubstratesofvelocity
encodinginthehealthyhuman orofacialsomatosensorysystemduring
saltatory(discontinuous, “jumping”) pneumotactileinputstotheunilateral
orofacialskin.Amultichannel, scalablepneumotactilearraywasusedto
presentstimulusvelocitiesat5cm/s,25cm/sand65cm/s.Thespatiotemporal
organizationofcorticalandsubcorticalBOLDresponseasafunctionofvelocity
wasanalyzedusing generallinearmodeling (GLM)ofsingle-subjectand
collapsedgroupfMRIsignaldata.
Galileo Somatosensory Array
Participants
• 14 R-handed, neurotypicaladults, 19-30years(M=21.2,SD=1.8)
StimulusDelivery
• Galileo Somatosensory array, programmed to generate sequential
saltatory stimuli (60 ms pulse duration, 10ms rise/fall)
• Custom-machined acetyl thermopolymer capsules (TAC-Cells)
arranged along a line (medial-lateral) spanning the right perioral
skin-to-cheek
fMRI Data Acquisition
Stimulus Velocity Control
ThisstudywassupportedbyagrantfromtheBarkleyTrustFoundation.
• Unilateral, sequential saltatory pneumotactile inputs to the lower
face produced localized, predominantly contralateral BOLD
responses in SI, SII, precentral and PPC, whose spatial organization
was dependent on velocity.1, 2
• BilateralSI,SII,andBOLDresponseintheinsularcortexwasnotedduring
slowvelocitypresentations(5cm/s,25cm/s).³
• HalfofthesubjectsshowedanipsilateralcerebellarBOLDresponseforthe
lowestvelocity(5cm/s)inregionsconsistentwiththedentate nucleus.4
• Resultsindicateadaptationviaascalabilityofnetworksprocessingtemporal
cuesassociatedwithvelocitypresentations
1. VenkatesanL,BarlowSM,PopescuM,PopescuA. Integrating approach
forstudying adaptationmechanismsinthehumansomatosensorycortical
network. ExperimentalBrainResearch 2014,232:3545-3554.
2. CusteadR,OhH,BarlowSM. Adaptation ofthecorticalsomatosensory
evokedpotentialfollowing pulsedpneumatic stimulationofthelowerface
inadults. BrainResearch 2015,1622:81-90.
3. AronoffR,MatyasF,MateoC,Ciron,C,SchneiderB,PetersonC. Long-
rangeconnectivityofmouseprimarysomatosensorybarrelcortex.
EuropeanJournalofNeuroscience 2010,31:2221-2233.
4. WardmanD,GandeviaS,ColebatchJ. Cerebral,subcortical, andcerebellar
activationevokedbyselectivestimulation ofmuscleandcutaneous
afferents:anfMRIstudy. PhysiologicalReports 2014,2(4):e00270.
Individual Whole-Brain GLM Analysis:
Main Effect of Velocity Condition
Block Design
ProgrammedtimedelaysbetweenpressurepulsesateachTAC-cellresultedin
5stimulusconditions: 5cm/s,25cm/s,65cm/s,ALL-ONsynchronous
activation, andALL-OFF
5velocityconditionswerepresentedinarandomizedblockdesign(20s
ON/20sOFF), 13.3min=1BOLD, 3BOLDsessions/subject
3TSiemensSkyra,32-channelheadcoil
• Anatomicalscan:(T1-weightedMPRAGE,0.9mmisotropic, TE=3.37ms,
TR=2400ms
• BOLDimages:(T2*-weightedEPI)brainvolume,41interleavedslices(2.5x
2.5x2.5mm³, TE=30ms,TR=2500ms),220mmFOVthatincludedorofacial
sensorimotorcortexandcerebellum
Subcortical Activation:
@ 5 cm/s
Group Whole-Brain Analysis:
Velocity vs. Control (ALL-OFF)
Cortical Response:
Deep Insular Response:
Subcortical - Cerebellar Response:
2015
Subject
Subject
It is the policy of the University of Nebraska-Lincoln not to discriminate based upon age, race, ethnicity,
color, national origin, gender, sex, pregnancy, disability, sexual orientation, genetic information,
veteran's status, marital status, religion or political affiliation.

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Custead_CB3_Poster v3

  • 1. ENCODING SALTATORY TACTILE VELOCITY IN THE HUMAN OROFACIAL SOMATOSENSORY SYSTEM USING fMRI Rebecca Custead, 1,3, Hyuntaek Oh 2,3, Steven M. Barlow 1-3 1Communication Disorders, 2Biological Systems Engineering, 3Center for Brain, Biology & Behavior, University of Nebraska, Lincoln, NE, USA Processingdynamic tactileinputsisakeyfunctionofsomatosensorysystems. Closelytiedtoskilled motoractivity, velocityencoding mechanismsare importantforfinemotorcontrol(speech,swallow,etc.). Knowledgeof sensoryprocessing networkscontributetoourunderstanding of sensorimotorrecoveryfollowing neurologicalinsult.Todate,littleisknown abouttactilevelocityencoding intrigeminalnetworksthatprocesscutaneous afferentinformation associated withfacialsensation, proprioception, and oromotorfeedback. Background Objective Methods Results Acknowledgements Conclusions References Tousehighresolution fMRItoinvestigatetheneuralsubstratesofvelocity encodinginthehealthyhuman orofacialsomatosensorysystemduring saltatory(discontinuous, “jumping”) pneumotactileinputstotheunilateral orofacialskin.Amultichannel, scalablepneumotactilearraywasusedto presentstimulusvelocitiesat5cm/s,25cm/sand65cm/s.Thespatiotemporal organizationofcorticalandsubcorticalBOLDresponseasafunctionofvelocity wasanalyzedusing generallinearmodeling (GLM)ofsingle-subjectand collapsedgroupfMRIsignaldata. Galileo Somatosensory Array Participants • 14 R-handed, neurotypicaladults, 19-30years(M=21.2,SD=1.8) StimulusDelivery • Galileo Somatosensory array, programmed to generate sequential saltatory stimuli (60 ms pulse duration, 10ms rise/fall) • Custom-machined acetyl thermopolymer capsules (TAC-Cells) arranged along a line (medial-lateral) spanning the right perioral skin-to-cheek fMRI Data Acquisition Stimulus Velocity Control ThisstudywassupportedbyagrantfromtheBarkleyTrustFoundation. • Unilateral, sequential saltatory pneumotactile inputs to the lower face produced localized, predominantly contralateral BOLD responses in SI, SII, precentral and PPC, whose spatial organization was dependent on velocity.1, 2 • BilateralSI,SII,andBOLDresponseintheinsularcortexwasnotedduring slowvelocitypresentations(5cm/s,25cm/s).³ • HalfofthesubjectsshowedanipsilateralcerebellarBOLDresponseforthe lowestvelocity(5cm/s)inregionsconsistentwiththedentate nucleus.4 • Resultsindicateadaptationviaascalabilityofnetworksprocessingtemporal cuesassociatedwithvelocitypresentations 1. VenkatesanL,BarlowSM,PopescuM,PopescuA. Integrating approach forstudying adaptationmechanismsinthehumansomatosensorycortical network. ExperimentalBrainResearch 2014,232:3545-3554. 2. CusteadR,OhH,BarlowSM. Adaptation ofthecorticalsomatosensory evokedpotentialfollowing pulsedpneumatic stimulationofthelowerface inadults. BrainResearch 2015,1622:81-90. 3. AronoffR,MatyasF,MateoC,Ciron,C,SchneiderB,PetersonC. Long- rangeconnectivityofmouseprimarysomatosensorybarrelcortex. EuropeanJournalofNeuroscience 2010,31:2221-2233. 4. WardmanD,GandeviaS,ColebatchJ. Cerebral,subcortical, andcerebellar activationevokedbyselectivestimulation ofmuscleandcutaneous afferents:anfMRIstudy. PhysiologicalReports 2014,2(4):e00270. Individual Whole-Brain GLM Analysis: Main Effect of Velocity Condition Block Design ProgrammedtimedelaysbetweenpressurepulsesateachTAC-cellresultedin 5stimulusconditions: 5cm/s,25cm/s,65cm/s,ALL-ONsynchronous activation, andALL-OFF 5velocityconditionswerepresentedinarandomizedblockdesign(20s ON/20sOFF), 13.3min=1BOLD, 3BOLDsessions/subject 3TSiemensSkyra,32-channelheadcoil • Anatomicalscan:(T1-weightedMPRAGE,0.9mmisotropic, TE=3.37ms, TR=2400ms • BOLDimages:(T2*-weightedEPI)brainvolume,41interleavedslices(2.5x 2.5x2.5mm³, TE=30ms,TR=2500ms),220mmFOVthatincludedorofacial sensorimotorcortexandcerebellum Subcortical Activation: @ 5 cm/s Group Whole-Brain Analysis: Velocity vs. Control (ALL-OFF) Cortical Response: Deep Insular Response: Subcortical - Cerebellar Response: 2015 Subject Subject It is the policy of the University of Nebraska-Lincoln not to discriminate based upon age, race, ethnicity, color, national origin, gender, sex, pregnancy, disability, sexual orientation, genetic information, veteran's status, marital status, religion or political affiliation.