Cargando…

The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm

Switch costs have been constantly found asymmetrical when switching between two tasks of unequal dominance. We used a combined Stroop-task-switching paradigm and recorded electroencephalographic (EEG) signals to explore the neural mechanism underlying the phenomenon of asymmetrical switch costs. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Shanshan, Hitchman, Glenn, Tan, Jinfeng, Zhao, Yuanfang, Tang, Dandan, Wang, Lijun, Chen, Antao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650803/
https://www.ncbi.nlm.nih.gov/pubmed/25989933
http://dx.doi.org/10.1038/srep10240
_version_ 1782401559766761472
author Wu, Shanshan
Hitchman, Glenn
Tan, Jinfeng
Zhao, Yuanfang
Tang, Dandan
Wang, Lijun
Chen, Antao
author_facet Wu, Shanshan
Hitchman, Glenn
Tan, Jinfeng
Zhao, Yuanfang
Tang, Dandan
Wang, Lijun
Chen, Antao
author_sort Wu, Shanshan
collection PubMed
description Switch costs have been constantly found asymmetrical when switching between two tasks of unequal dominance. We used a combined Stroop-task-switching paradigm and recorded electroencephalographic (EEG) signals to explore the neural mechanism underlying the phenomenon of asymmetrical switch costs. The results revealed that a fronto-central N2 component demonstrated greater negativity in word switch (cW) trials relative to word repeat (wW) trials, and both First P3 and P3b components over the parieto-central region exhibited greater positivity in color switch (wC) trials relative to color repeat (cC) trials, whereas a contrasting switch-related fronto-central SP effect was found to have an opposite pattern for each task. Moreover, the time-frequency analysis showed a right-frontal lower alpha band (9-11 Hz) modulation in the word task, whereas a fronto-central upper alpha band (11-13 Hz) modulation was exclusively found in the color task. These results provide evidence for dissociable neural processes, which are related to inhibitory control and endogenous control, contributing to the generation of asymmetrical switch costs.
format Online
Article
Text
id pubmed-4650803
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-46508032015-11-24 The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm Wu, Shanshan Hitchman, Glenn Tan, Jinfeng Zhao, Yuanfang Tang, Dandan Wang, Lijun Chen, Antao Sci Rep Article Switch costs have been constantly found asymmetrical when switching between two tasks of unequal dominance. We used a combined Stroop-task-switching paradigm and recorded electroencephalographic (EEG) signals to explore the neural mechanism underlying the phenomenon of asymmetrical switch costs. The results revealed that a fronto-central N2 component demonstrated greater negativity in word switch (cW) trials relative to word repeat (wW) trials, and both First P3 and P3b components over the parieto-central region exhibited greater positivity in color switch (wC) trials relative to color repeat (cC) trials, whereas a contrasting switch-related fronto-central SP effect was found to have an opposite pattern for each task. Moreover, the time-frequency analysis showed a right-frontal lower alpha band (9-11 Hz) modulation in the word task, whereas a fronto-central upper alpha band (11-13 Hz) modulation was exclusively found in the color task. These results provide evidence for dissociable neural processes, which are related to inhibitory control and endogenous control, contributing to the generation of asymmetrical switch costs. Nature Publishing Group 2015-05-20 /pmc/articles/PMC4650803/ /pubmed/25989933 http://dx.doi.org/10.1038/srep10240 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wu, Shanshan
Hitchman, Glenn
Tan, Jinfeng
Zhao, Yuanfang
Tang, Dandan
Wang, Lijun
Chen, Antao
The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm
title The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm
title_full The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm
title_fullStr The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm
title_full_unstemmed The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm
title_short The neural dynamic mechanisms of asymmetric switch costs in a combined Stroop-task-switching paradigm
title_sort neural dynamic mechanisms of asymmetric switch costs in a combined stroop-task-switching paradigm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650803/
https://www.ncbi.nlm.nih.gov/pubmed/25989933
http://dx.doi.org/10.1038/srep10240
work_keys_str_mv AT wushanshan theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT hitchmanglenn theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT tanjinfeng theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT zhaoyuanfang theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT tangdandan theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT wanglijun theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT chenantao theneuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT wushanshan neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT hitchmanglenn neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT tanjinfeng neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT zhaoyuanfang neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT tangdandan neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT wanglijun neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm
AT chenantao neuraldynamicmechanismsofasymmetricswitchcostsinacombinedstrooptaskswitchingparadigm