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Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study
In predictable contexts, motor inhibitory control can be deployed before the actual need for response suppression. The brain functional underpinnings of proactive inhibition, and notably the role of basal ganglia, are not entirely identified. We investigated the effects of deep brain stimulation of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288097/ https://www.ncbi.nlm.nih.gov/pubmed/34110074 http://dx.doi.org/10.1002/hbm.25530 |
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author | De Pretto, Michael Mouthon, Michael Debove, Ines Pollo, Claudio Schüpbach, Michael Spierer, Lucas Accolla, Ettore A. |
author_facet | De Pretto, Michael Mouthon, Michael Debove, Ines Pollo, Claudio Schüpbach, Michael Spierer, Lucas Accolla, Ettore A. |
author_sort | De Pretto, Michael |
collection | PubMed |
description | In predictable contexts, motor inhibitory control can be deployed before the actual need for response suppression. The brain functional underpinnings of proactive inhibition, and notably the role of basal ganglia, are not entirely identified. We investigated the effects of deep brain stimulation of the subthalamic nucleus or internal globus pallidus on proactive inhibition in patients with Parkinson's disease. They completed a cued go/no‐go proactive inhibition task ON and (unilateral) OFF stimulation while EEG was recorded. We found no behavioural effect of either subthalamic nucleus or internal globus pallidus deep brain stimulation on proactive inhibition, despite a general improvement of motor performance with subthalamic nucleus stimulation. In the non‐operated and subthalamic nucleus group, we identified periods of topographic EEG modulation by the level of proactive inhibition. In the subthalamic nucleus group, source estimation analysis suggested the initial involvement of bilateral frontal and occipital areas, followed by a right lateralized fronto‐basal network, and finally of right premotor and left parietal regions. Our results confirm the overall preservation of proactive inhibition capacities in both subthalamic nucleus and internal globus pallidus deep brain stimulation, and suggest a partly segregated network for proactive inhibition, with a preferential recruitment of the indirect pathway. |
format | Online Article Text |
id | pubmed-8288097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82880972021-07-21 Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study De Pretto, Michael Mouthon, Michael Debove, Ines Pollo, Claudio Schüpbach, Michael Spierer, Lucas Accolla, Ettore A. Hum Brain Mapp Research Articles In predictable contexts, motor inhibitory control can be deployed before the actual need for response suppression. The brain functional underpinnings of proactive inhibition, and notably the role of basal ganglia, are not entirely identified. We investigated the effects of deep brain stimulation of the subthalamic nucleus or internal globus pallidus on proactive inhibition in patients with Parkinson's disease. They completed a cued go/no‐go proactive inhibition task ON and (unilateral) OFF stimulation while EEG was recorded. We found no behavioural effect of either subthalamic nucleus or internal globus pallidus deep brain stimulation on proactive inhibition, despite a general improvement of motor performance with subthalamic nucleus stimulation. In the non‐operated and subthalamic nucleus group, we identified periods of topographic EEG modulation by the level of proactive inhibition. In the subthalamic nucleus group, source estimation analysis suggested the initial involvement of bilateral frontal and occipital areas, followed by a right lateralized fronto‐basal network, and finally of right premotor and left parietal regions. Our results confirm the overall preservation of proactive inhibition capacities in both subthalamic nucleus and internal globus pallidus deep brain stimulation, and suggest a partly segregated network for proactive inhibition, with a preferential recruitment of the indirect pathway. John Wiley & Sons, Inc. 2021-06-10 /pmc/articles/PMC8288097/ /pubmed/34110074 http://dx.doi.org/10.1002/hbm.25530 Text en © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles De Pretto, Michael Mouthon, Michael Debove, Ines Pollo, Claudio Schüpbach, Michael Spierer, Lucas Accolla, Ettore A. Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study |
title | Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study |
title_full | Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study |
title_fullStr | Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study |
title_full_unstemmed | Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study |
title_short | Proactive inhibition is not modified by deep brain stimulation for Parkinson's disease: An electrical neuroimaging study |
title_sort | proactive inhibition is not modified by deep brain stimulation for parkinson's disease: an electrical neuroimaging study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288097/ https://www.ncbi.nlm.nih.gov/pubmed/34110074 http://dx.doi.org/10.1002/hbm.25530 |
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