Cognitive flexibility and N2/P3 event-related brain potentials

Abstract Task switching is often considered for evaluating limitations of cognitive flexibility. Switch costs are behavioural indices of limited cognitive flexibility, and switch costs may be decomposable into stimulus- and response-related fractions, as conjectured by the domain hypothesis of cogni...

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Main Authors: Bruno Kopp, Alexander Steinke, Antonino Visalli
Format: Article
Language:English
Published: Nature Publishing Group 2020-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-020-66781-5
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spelling doaj-e3bb1c5569d84daca97565e931be770b2021-06-20T11:42:01ZengNature Publishing GroupScientific Reports2045-23222020-06-0110111710.1038/s41598-020-66781-5Cognitive flexibility and N2/P3 event-related brain potentialsBruno Kopp0Alexander Steinke1Antonino Visalli2Department of Neurology, Hannover Medical SchoolDepartment of Neurology, Hannover Medical SchoolDepartment of Neurology, Hannover Medical SchoolAbstract Task switching is often considered for evaluating limitations of cognitive flexibility. Switch costs are behavioural indices of limited cognitive flexibility, and switch costs may be decomposable into stimulus- and response-related fractions, as conjectured by the domain hypothesis of cognitive flexibility. According to the domain hypothesis, there exist separable stimulus- and response-related neural networks for cognitive flexibility, which should be discernible as distinct event-related potentials (ERPs). The present card-matching study allowed isolating stimulus- and response-related switch costs, while measuring ERPs evoked by task cues and target stimuli with a focus on the target-locked N2/P3 complex. Behavioural data revealed that both stimulus-task and response-task bindings contribute to switch costs. Cue-locked ERPs yielded larger anterior negativity/posterior positivity in response to switch cues compared to repeat cues. Target-locked ERPs revealed separable ERP correlates of stimulus- and response-related switch costs. P3 waveforms with fronto-central scalp distributions emerged as a corollary of stimulus-related switch costs. Fronto-centrally distributed N2 waveforms occurred when stimulus-task and response-task bindings contributed jointly to switch costs. The reported N2/P3 ERP data are commensurate with the domain hypothesis according to which there exist separable stimulus- and response-related neural networks for cognitive flexibility.https://doi.org/10.1038/s41598-020-66781-5
collection DOAJ
language English
format Article
sources DOAJ
author Bruno Kopp
Alexander Steinke
Antonino Visalli
spellingShingle Bruno Kopp
Alexander Steinke
Antonino Visalli
Cognitive flexibility and N2/P3 event-related brain potentials
Scientific Reports
author_facet Bruno Kopp
Alexander Steinke
Antonino Visalli
author_sort Bruno Kopp
title Cognitive flexibility and N2/P3 event-related brain potentials
title_short Cognitive flexibility and N2/P3 event-related brain potentials
title_full Cognitive flexibility and N2/P3 event-related brain potentials
title_fullStr Cognitive flexibility and N2/P3 event-related brain potentials
title_full_unstemmed Cognitive flexibility and N2/P3 event-related brain potentials
title_sort cognitive flexibility and n2/p3 event-related brain potentials
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2020-06-01
description Abstract Task switching is often considered for evaluating limitations of cognitive flexibility. Switch costs are behavioural indices of limited cognitive flexibility, and switch costs may be decomposable into stimulus- and response-related fractions, as conjectured by the domain hypothesis of cognitive flexibility. According to the domain hypothesis, there exist separable stimulus- and response-related neural networks for cognitive flexibility, which should be discernible as distinct event-related potentials (ERPs). The present card-matching study allowed isolating stimulus- and response-related switch costs, while measuring ERPs evoked by task cues and target stimuli with a focus on the target-locked N2/P3 complex. Behavioural data revealed that both stimulus-task and response-task bindings contribute to switch costs. Cue-locked ERPs yielded larger anterior negativity/posterior positivity in response to switch cues compared to repeat cues. Target-locked ERPs revealed separable ERP correlates of stimulus- and response-related switch costs. P3 waveforms with fronto-central scalp distributions emerged as a corollary of stimulus-related switch costs. Fronto-centrally distributed N2 waveforms occurred when stimulus-task and response-task bindings contributed jointly to switch costs. The reported N2/P3 ERP data are commensurate with the domain hypothesis according to which there exist separable stimulus- and response-related neural networks for cognitive flexibility.
url https://doi.org/10.1038/s41598-020-66781-5
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