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dc.contributor.authorKohl, Carmen
dc.contributor.authorParviainen, Tiina
dc.contributor.authorJones, Stephanie R.
dc.date.accessioned2021-04-28T11:57:55Z
dc.date.available2021-04-28T11:57:55Z
dc.date.issued2022
dc.identifier.citationKohl, C., Parviainen, T., & Jones, S. R. (2022). Neural Mechanisms Underlying Human Auditory Evoked Responses Revealed By Human Neocortical Neurosolver. <i>Brain Topography</i>, <i>35</i>(1), 19-35. <a href="https://doi.org/10.1007/s10548-021-00838-0" target="_blank">https://doi.org/10.1007/s10548-021-00838-0</a>
dc.identifier.otherCONVID_68041749
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/75241
dc.description.abstractAuditory evoked fields (AEFs) are commonly studied, yet their underlying neural mechanisms remain poorly understood. Here, we used the biophysical modelling software Human Neocortical Neurosolver (HNN) whose foundation is a canonical neocortical circuit model to interpret the cell and network mechanisms contributing to macroscale AEFs elicited by a simple tone, measured with magnetoencephalography. We found that AEFs can be reproduced by activating the neocortical circuit through a layer specific sequence of feedforward and feedback excitatory synaptic drives, similar to prior simulation of somatosensory evoked responses, supporting the notion that basic structures and activation patterns are preserved across sensory regions. We also applied the modeling framework to develop and test predictions on neural mechanisms underlying AEF differences in the left and right hemispheres, as well as in hemispheres contralateral and ipsilateral to the presentation of the auditory stimulus. We found that increasing the strength of the excitatory synaptic cortical feedback inputs to supragranular layers simulates the commonly observed right hemisphere dominance, while decreasing the input latencies and simultaneously increasing the number of cells contributing to the signal accounted for the contralateral dominance. These results provide a direct link between human data and prior animal studies and lay the foundation for future translational research examining the mechanisms underlying alteration in this fundamental biomarker of auditory processing in healthy cognition and neuropathology.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofseriesBrain Topography
dc.rightsCC BY 4.0
dc.subject.otherauditory processing
dc.subject.otherAEF
dc.subject.otherMEG
dc.subject.otherbiophysical model
dc.subject.otherHNN
dc.titleNeural Mechanisms Underlying Human Auditory Evoked Responses Revealed By Human Neocortical Neurosolver
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202104282551
dc.contributor.laitosPsykologian laitosfi
dc.contributor.laitosDepartment of Psychologyen
dc.contributor.oppiaineMonitieteinen aivotutkimuskeskusfi
dc.contributor.oppiainePsykologiafi
dc.contributor.oppiaineHyvinvoinnin tutkimuksen yhteisöfi
dc.contributor.oppiaineCentre for Interdisciplinary Brain Researchen
dc.contributor.oppiainePsychologyen
dc.contributor.oppiaineSchool of Wellbeingen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange19-35
dc.relation.issn0896-0267
dc.relation.numberinseries1
dc.relation.volume35
dc.type.versionpublishedVersion
dc.rights.copyright© 2021 the Authors
dc.rights.accesslevelopenAccessfi
dc.subject.ysoMEG
dc.subject.ysokuulohavainnot
dc.subject.ysohermoverkot (biologia)
dc.subject.ysobiofysiikka
dc.subject.ysokognitiivinen neurotiede
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p3329
jyx.subject.urihttp://www.yso.fi/onto/yso/p23127
jyx.subject.urihttp://www.yso.fi/onto/yso/p38811
jyx.subject.urihttp://www.yso.fi/onto/yso/p6097
jyx.subject.urihttp://www.yso.fi/onto/yso/p23133
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1007/s10548-021-00838-0
jyx.fundinginformationThis study was supported by National Institutes of Health (Grant Nos. NIBIB RO1 EB022889, NIMH RO1 MH106174).
dc.type.okmA1


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