How salience enhances inhibitory control : An analysis of electro-cortical mechanisms
Kenemans, J. L., Schutte, I., Van Bijnen, S., & Logemann, H. A. (2023). How salience enhances inhibitory control : An analysis of electro-cortical mechanisms. Biological Psychology, 177, Article 108505. https://doi.org/10.1016/j.biopsycho.2023.108505
Julkaistu sarjassa
Biological PsychologyPäivämäärä
2023Oppiaine
PsykologiaMonitieteinen aivotutkimuskeskusHyvinvoinnin tutkimuksen yhteisöPsychologyCentre for Interdisciplinary Brain ResearchSchool of WellbeingTekijänoikeudet
© 2023 The Authors. Published by Elsevier B.V.
Stop-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.
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Elsevier BVISSN Hae Julkaisufoorumista
0301-0511Asiasanat
Julkaisu tutkimustietojärjestelmässä
https://converis.jyu.fi/converis/portal/detail/Publication/176625046
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Lisätietoja rahoituksesta
Hungarian National Research, Development and Innovation Office (Grant no. K131635) for H.N.A.L.Lisenssi
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