Cargando…
Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing
Growing evidence suggests that both the medial prefrontal cortex (mPFC) and the subthalamic nucleus (STN) play crucial roles in conflict processing, but how these two structures coordinate their activities remains poorly understood. We simultaneously recorded electroencephalogram from the mPFC and l...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944202/ https://www.ncbi.nlm.nih.gov/pubmed/34077804 http://dx.doi.org/10.1016/j.neuroimage.2021.118205 |
_version_ | 1784673669055774720 |
---|---|
author | Zeng, Ke Drummond, Neil M. Ghahremani, Ayda Saha, Utpal Kalia, Suneil K. Hodaie, Mojgan Lozano, Andres M. Aron, Adam R. Chen, Robert |
author_facet | Zeng, Ke Drummond, Neil M. Ghahremani, Ayda Saha, Utpal Kalia, Suneil K. Hodaie, Mojgan Lozano, Andres M. Aron, Adam R. Chen, Robert |
author_sort | Zeng, Ke |
collection | PubMed |
description | Growing evidence suggests that both the medial prefrontal cortex (mPFC) and the subthalamic nucleus (STN) play crucial roles in conflict processing, but how these two structures coordinate their activities remains poorly understood. We simultaneously recorded electroencephalogram from the mPFC and local field potentials from the STN using deep brain stimulation electrodes in 13 Parkinson’s disease patients while they performed a Stroop task. Both mPFC and STN showed significant increases in theta activities (2–8 Hz) in incongruent trials compared to the congruent trials. The theta activity in incongruent trials also demonstrated significantly increased phase synchronization between mPFC and STN. Furthermore, the amplitude of gamma oscillation was modulated by the phase of theta activity at the STN in incongruent trials. Such theta-gamma phase-amplitude coupling (PAC) was much stronger for incongruent trials with faster reaction times than those with slower reaction times. Elevated theta-gamma PAC in the STN provides a novel mechanism by which the STN may operationalize its proposed “hold-your-horses” role. The co-occurrence of mPFC-STN theta phase synchronization and STN theta-gamma PAC reflects a neural substrate for fronto-subthalamic communication during conflict processing. More broadly, it may be a general mechanism for neuronal interactions in the cortico-basal ganglia circuits via a combination of long-range, within-frequency phase synchronization and local cross-frequency PAC. |
format | Online Article Text |
id | pubmed-8944202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-89442022022-03-24 Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing Zeng, Ke Drummond, Neil M. Ghahremani, Ayda Saha, Utpal Kalia, Suneil K. Hodaie, Mojgan Lozano, Andres M. Aron, Adam R. Chen, Robert Neuroimage Article Growing evidence suggests that both the medial prefrontal cortex (mPFC) and the subthalamic nucleus (STN) play crucial roles in conflict processing, but how these two structures coordinate their activities remains poorly understood. We simultaneously recorded electroencephalogram from the mPFC and local field potentials from the STN using deep brain stimulation electrodes in 13 Parkinson’s disease patients while they performed a Stroop task. Both mPFC and STN showed significant increases in theta activities (2–8 Hz) in incongruent trials compared to the congruent trials. The theta activity in incongruent trials also demonstrated significantly increased phase synchronization between mPFC and STN. Furthermore, the amplitude of gamma oscillation was modulated by the phase of theta activity at the STN in incongruent trials. Such theta-gamma phase-amplitude coupling (PAC) was much stronger for incongruent trials with faster reaction times than those with slower reaction times. Elevated theta-gamma PAC in the STN provides a novel mechanism by which the STN may operationalize its proposed “hold-your-horses” role. The co-occurrence of mPFC-STN theta phase synchronization and STN theta-gamma PAC reflects a neural substrate for fronto-subthalamic communication during conflict processing. More broadly, it may be a general mechanism for neuronal interactions in the cortico-basal ganglia circuits via a combination of long-range, within-frequency phase synchronization and local cross-frequency PAC. 2021-09 2021-05-30 /pmc/articles/PMC8944202/ /pubmed/34077804 http://dx.doi.org/10.1016/j.neuroimage.2021.118205 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Article Zeng, Ke Drummond, Neil M. Ghahremani, Ayda Saha, Utpal Kalia, Suneil K. Hodaie, Mojgan Lozano, Andres M. Aron, Adam R. Chen, Robert Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
title | Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
title_full | Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
title_fullStr | Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
title_full_unstemmed | Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
title_short | Fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
title_sort | fronto-subthalamic phase synchronization and cross-frequency coupling during conflict processing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944202/ https://www.ncbi.nlm.nih.gov/pubmed/34077804 http://dx.doi.org/10.1016/j.neuroimage.2021.118205 |
work_keys_str_mv | AT zengke frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT drummondneilm frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT ghahremaniayda frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT sahautpal frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT kaliasuneilk frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT hodaiemojgan frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT lozanoandresm frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT aronadamr frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing AT chenrobert frontosubthalamicphasesynchronizationandcrossfrequencycouplingduringconflictprocessing |