Cargando…

Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition

Reward and cognitive control play crucial roles in shaping goal-directed behavior. Yet, the behavioral and neural underpinnings of interactive effects of both processes in driving our actions towards a particular goal have remained rather unclear. Given the importance of inhibitory control, we inves...

Descripción completa

Detalles Bibliográficos
Autores principales: Koyun, Anna Helin, Stock, Ann-Kathrin, Beste, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322977/
https://www.ncbi.nlm.nih.gov/pubmed/37407656
http://dx.doi.org/10.1038/s41598-023-37524-z
_version_ 1785068876794429440
author Koyun, Anna Helin
Stock, Ann-Kathrin
Beste, Christian
author_facet Koyun, Anna Helin
Stock, Ann-Kathrin
Beste, Christian
author_sort Koyun, Anna Helin
collection PubMed
description Reward and cognitive control play crucial roles in shaping goal-directed behavior. Yet, the behavioral and neural underpinnings of interactive effects of both processes in driving our actions towards a particular goal have remained rather unclear. Given the importance of inhibitory control, we investigated the effect of reward prospect on the modulatory influence of automatic versus controlled processes during response inhibition. For this, a performance-contingent monetary reward for both correct response selection and response inhibition was added to a Simon NoGo task, which manipulates the relationship of automatic and controlled processes in Go and NoGo trials. A neurophysiological approach was used by combining EEG temporal signal decomposition and source localization methods. Compared to a non-rewarded control group, rewarded participants showed faster response execution, as well as overall lower response selection and inhibition accuracy (shifted speed-accuracy tradeoff). Interestingly, the reward group displayed a larger interference of the interactive effects of automatic versus controlled processes during response inhibition (i.e., a larger Simon NoGo effect), but not during response selection. The reward-specific behavioral effect was mirrored by the P3 amplitude, underlining the importance of stimulus–response association processes in explaining variability in response inhibition performance. The selective reward-induced neurophysiological modulation was associated with lower activation differences in relevant structures spanning the inferior frontal and parietal cortex, as well as higher activation differences in the somatosensory cortex. Taken together, this study highlights relevant neuroanatomical structures underlying selective reward effects on response inhibition and extends previous reports on the possible detrimental effect of reward-triggered performance trade-offs on cognitive control processes.
format Online
Article
Text
id pubmed-10322977
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-103229772023-07-07 Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition Koyun, Anna Helin Stock, Ann-Kathrin Beste, Christian Sci Rep Article Reward and cognitive control play crucial roles in shaping goal-directed behavior. Yet, the behavioral and neural underpinnings of interactive effects of both processes in driving our actions towards a particular goal have remained rather unclear. Given the importance of inhibitory control, we investigated the effect of reward prospect on the modulatory influence of automatic versus controlled processes during response inhibition. For this, a performance-contingent monetary reward for both correct response selection and response inhibition was added to a Simon NoGo task, which manipulates the relationship of automatic and controlled processes in Go and NoGo trials. A neurophysiological approach was used by combining EEG temporal signal decomposition and source localization methods. Compared to a non-rewarded control group, rewarded participants showed faster response execution, as well as overall lower response selection and inhibition accuracy (shifted speed-accuracy tradeoff). Interestingly, the reward group displayed a larger interference of the interactive effects of automatic versus controlled processes during response inhibition (i.e., a larger Simon NoGo effect), but not during response selection. The reward-specific behavioral effect was mirrored by the P3 amplitude, underlining the importance of stimulus–response association processes in explaining variability in response inhibition performance. The selective reward-induced neurophysiological modulation was associated with lower activation differences in relevant structures spanning the inferior frontal and parietal cortex, as well as higher activation differences in the somatosensory cortex. Taken together, this study highlights relevant neuroanatomical structures underlying selective reward effects on response inhibition and extends previous reports on the possible detrimental effect of reward-triggered performance trade-offs on cognitive control processes. Nature Publishing Group UK 2023-07-05 /pmc/articles/PMC10322977/ /pubmed/37407656 http://dx.doi.org/10.1038/s41598-023-37524-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Koyun, Anna Helin
Stock, Ann-Kathrin
Beste, Christian
Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
title Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
title_full Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
title_fullStr Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
title_full_unstemmed Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
title_short Neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
title_sort neurophysiological mechanisms underlying the differential effect of reward prospect on response selection and inhibition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322977/
https://www.ncbi.nlm.nih.gov/pubmed/37407656
http://dx.doi.org/10.1038/s41598-023-37524-z
work_keys_str_mv AT koyunannahelin neurophysiologicalmechanismsunderlyingthedifferentialeffectofrewardprospectonresponseselectionandinhibition
AT stockannkathrin neurophysiologicalmechanismsunderlyingthedifferentialeffectofrewardprospectonresponseselectionandinhibition
AT bestechristian neurophysiologicalmechanismsunderlyingthedifferentialeffectofrewardprospectonresponseselectionandinhibition