Cargando…

Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance

The functional role of the right inferior frontal cortex (rIFC) in mediating human behavior is the subject of ongoing debate. Activation of the rIFC has been associated with both response inhibition and with signaling action adaptation demands resulting from unpredicted events. The goal of this stud...

Descripción completa

Detalles Bibliográficos
Autores principales: van Campen, A. Dilene, Neubert, Franz-Xaver, van den Wildenberg, Wery P. M., Ridderinkhof, K. Richard, Mars, Rogier B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825091/
https://www.ncbi.nlm.nih.gov/pubmed/24282398
http://dx.doi.org/10.3389/fnhum.2013.00736
_version_ 1782290767757180928
author van Campen, A. Dilene
Neubert, Franz-Xaver
van den Wildenberg, Wery P. M.
Ridderinkhof, K. Richard
Mars, Rogier B.
author_facet van Campen, A. Dilene
Neubert, Franz-Xaver
van den Wildenberg, Wery P. M.
Ridderinkhof, K. Richard
Mars, Rogier B.
author_sort van Campen, A. Dilene
collection PubMed
description The functional role of the right inferior frontal cortex (rIFC) in mediating human behavior is the subject of ongoing debate. Activation of the rIFC has been associated with both response inhibition and with signaling action adaptation demands resulting from unpredicted events. The goal of this study is to investigate the role of rIFC by combining a go/no-go paradigm with paired-pulse transcranial magnetic stimulation (ppTMS) over rIFC and the primary motor cortex (M1) to probe the functional connectivity between these brain areas. Participants performed a go/no-go task with 20% or 80% of the trials requiring response inhibition (no-go trials) in a classic and a reversed version of the task, respectively. Responses were slower to infrequent compared to frequent go trials, while commission errors were more prevalent to infrequent compared to frequent no-go trials. We hypothesized that if rIFC is involved primarily in response inhibition, then rIFC should exert an inhibitory influence over M1 on no-go (inhibition) trials regardless of no-go probability. If, by contrast, rIFC has a role on unexpected trials other than just response inhibition then rIFC should influence M1 on infrequent trials regardless of response demands. We observed that rIFC suppressed M1 excitability during frequent no-go trials, but not during infrequent no-go trials, suggesting that the role of rIFC in response inhibition is context dependent rather than generic. Importantly, rIFC was found to facilitate M1 excitability on all low frequent trials, irrespective of whether the infrequent event involved response inhibition, a finding more in line with a predictive coding framework of cognitive control.
format Online
Article
Text
id pubmed-3825091
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-38250912013-11-26 Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance van Campen, A. Dilene Neubert, Franz-Xaver van den Wildenberg, Wery P. M. Ridderinkhof, K. Richard Mars, Rogier B. Front Hum Neurosci Neuroscience The functional role of the right inferior frontal cortex (rIFC) in mediating human behavior is the subject of ongoing debate. Activation of the rIFC has been associated with both response inhibition and with signaling action adaptation demands resulting from unpredicted events. The goal of this study is to investigate the role of rIFC by combining a go/no-go paradigm with paired-pulse transcranial magnetic stimulation (ppTMS) over rIFC and the primary motor cortex (M1) to probe the functional connectivity between these brain areas. Participants performed a go/no-go task with 20% or 80% of the trials requiring response inhibition (no-go trials) in a classic and a reversed version of the task, respectively. Responses were slower to infrequent compared to frequent go trials, while commission errors were more prevalent to infrequent compared to frequent no-go trials. We hypothesized that if rIFC is involved primarily in response inhibition, then rIFC should exert an inhibitory influence over M1 on no-go (inhibition) trials regardless of no-go probability. If, by contrast, rIFC has a role on unexpected trials other than just response inhibition then rIFC should influence M1 on infrequent trials regardless of response demands. We observed that rIFC suppressed M1 excitability during frequent no-go trials, but not during infrequent no-go trials, suggesting that the role of rIFC in response inhibition is context dependent rather than generic. Importantly, rIFC was found to facilitate M1 excitability on all low frequent trials, irrespective of whether the infrequent event involved response inhibition, a finding more in line with a predictive coding framework of cognitive control. Frontiers Media S.A. 2013-11-12 /pmc/articles/PMC3825091/ /pubmed/24282398 http://dx.doi.org/10.3389/fnhum.2013.00736 Text en Copyright © 2013 van Campen, Neubert, van den Wildenberg, Ridderinkhof and Mars. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
van Campen, A. Dilene
Neubert, Franz-Xaver
van den Wildenberg, Wery P. M.
Ridderinkhof, K. Richard
Mars, Rogier B.
Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
title Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
title_full Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
title_fullStr Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
title_full_unstemmed Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
title_short Paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
title_sort paired-pulse transcranial magnetic stimulation reveals probability-dependent changes in functional connectivity between right inferior frontal cortex and primary motor cortex during go/no-go performance
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825091/
https://www.ncbi.nlm.nih.gov/pubmed/24282398
http://dx.doi.org/10.3389/fnhum.2013.00736
work_keys_str_mv AT vancampenadilene pairedpulsetranscranialmagneticstimulationrevealsprobabilitydependentchangesinfunctionalconnectivitybetweenrightinferiorfrontalcortexandprimarymotorcortexduringgonogoperformance
AT neubertfranzxaver pairedpulsetranscranialmagneticstimulationrevealsprobabilitydependentchangesinfunctionalconnectivitybetweenrightinferiorfrontalcortexandprimarymotorcortexduringgonogoperformance
AT vandenwildenbergwerypm pairedpulsetranscranialmagneticstimulationrevealsprobabilitydependentchangesinfunctionalconnectivitybetweenrightinferiorfrontalcortexandprimarymotorcortexduringgonogoperformance
AT ridderinkhofkrichard pairedpulsetranscranialmagneticstimulationrevealsprobabilitydependentchangesinfunctionalconnectivitybetweenrightinferiorfrontalcortexandprimarymotorcortexduringgonogoperformance
AT marsrogierb pairedpulsetranscranialmagneticstimulationrevealsprobabilitydependentchangesinfunctionalconnectivitybetweenrightinferiorfrontalcortexandprimarymotorcortexduringgonogoperformance