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dc.contributor.authorKenemans, J. Leon
dc.contributor.authorSchutte, Iris
dc.contributor.authorVan Bijnen, Sam
dc.contributor.authorLogemann, H.N. Alexander
dc.date.accessioned2023-02-08T05:34:45Z
dc.date.available2023-02-08T05:34:45Z
dc.date.issued2023
dc.identifier.citationKenemans, J. L., Schutte, I., Van Bijnen, S., & Logemann, H. A. (2023). How salience enhances inhibitory control : An analysis of electro-cortical mechanisms. <i>Biological Psychology</i>, <i>177</i>, Article 108505. <a href="https://doi.org/10.1016/j.biopsycho.2023.108505" target="_blank">https://doi.org/10.1016/j.biopsycho.2023.108505</a>
dc.identifier.otherCONVID_176625046
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/85388
dc.description.abstractStop-signal tasks (SSTs) combined with human electro-cortical recordings (Event-Related Potentials, ERPs) have revealed mechanisms associated with successful stopping (relative to failed), presumably contributing to inhibitory control. The corresponding ERP signatures have been labeled stop N1 (+/- 100-ms latency), stop N2 (200 ms), and stop P3 (160–250 ms), and argued to reflect more sensory-specific (N1) versus more generic (N2, P3) mechanisms. However, stop N1 and stop N2, as well as latencies of stop-P3, appear to be quite inconsistent across studies. The present work addressed the possible influence of stop-signal salience, expecting high salience to induce clear stop N1s but reduced stop N2s, and short-latency stop P3s. Three SST varieties were combined with high-resolution EEG. An imperative visual (go) stimulus was occasionally followed by a subsequent (stop) stimulus that signalled to withhold the just initiated response. Stop-Signal Reaction Times (SSRTs) decreased linearly from visual-low to visual-high-salience to auditory. Auditory Stop N1 was replicated. A C1-like visual evoked potential (latency < 100 ms) was observed only with high salience, but not robustly associated with successful versus failed stops. Using the successful-failed contrast a visual stop-N1 analogue (112–156 ms post-stop-signal) was identified, as was right-frontal stop N2, but neither was sensitive to salience. Stop P3 had shorter latency for high than for low salience, and the extent of the early high-salience stop P3 correlated inversely with SSRT. These results suggest that salience-enhanced inhibitory control as manifest in SSRTs is associated with generic rather than sensory-specific electrocortical mechanisms.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.ispartofseriesBiological Psychology
dc.rightsCC BY 4.0
dc.subject.otherinhibitory control
dc.subject.othersensory-specific versus generic
dc.subject.otherEEG/ ERP
dc.subject.othersalience
dc.subject.otherelectro-cortical mechanisms
dc.titleHow salience enhances inhibitory control : An analysis of electro-cortical mechanisms
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202302081668
dc.contributor.laitosPsykologian laitosfi
dc.contributor.laitosDepartment of Psychologyen
dc.contributor.oppiainePsykologiafi
dc.contributor.oppiaineMonitieteinen aivotutkimuskeskusfi
dc.contributor.oppiaineHyvinvoinnin tutkimuksen yhteisöfi
dc.contributor.oppiainePsychologyen
dc.contributor.oppiaineCentre for Interdisciplinary Brain Researchen
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.relation.issn0301-0511
dc.relation.volume177
dc.type.versionpublishedVersion
dc.rights.copyright© 2023 The Authors. Published by Elsevier B.V.
dc.rights.accesslevelopenAccessfi
dc.subject.ysokognitiivinen neurotiede
dc.subject.ysokäyttäytyminen
dc.subject.ysoaivokuori
dc.subject.ysoitsehallinta
dc.subject.ysoEEG
dc.subject.ysoelektrofysiologia
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p23133
jyx.subject.urihttp://www.yso.fi/onto/yso/p3625
jyx.subject.urihttp://www.yso.fi/onto/yso/p7039
jyx.subject.urihttp://www.yso.fi/onto/yso/p17219
jyx.subject.urihttp://www.yso.fi/onto/yso/p3328
jyx.subject.urihttp://www.yso.fi/onto/yso/p7871
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1016/j.biopsycho.2023.108505
jyx.fundinginformationHungarian National Research, Development and Innovation Office (Grant no. K131635) for H.N.A.L.
dc.type.okmA1


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