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Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements

In humans, the ability to withhold manual motor responses seems to rely on a right-lateralized frontal–basal ganglia–thalamic network, including the pre-supplementary motor area and the inferior frontal gyrus (IFG). These areas should drive subthalamic nuclei to implement movement inhibition via the...

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Autores principales: Mattia, M., Spadacenta, S., Pavone, L., Quarato, P., Esposito, V., Sparano, A., Sebastiano, F., Di Gennaro, G., Morace, R., Cantore, G., Mirabella, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386527/
https://www.ncbi.nlm.nih.gov/pubmed/22754525
http://dx.doi.org/10.3389/fneng.2012.00012
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author Mattia, M.
Spadacenta, S.
Pavone, L.
Quarato, P.
Esposito, V.
Sparano, A.
Sebastiano, F.
Di Gennaro, G.
Morace, R.
Cantore, G.
Mirabella, G.
author_facet Mattia, M.
Spadacenta, S.
Pavone, L.
Quarato, P.
Esposito, V.
Sparano, A.
Sebastiano, F.
Di Gennaro, G.
Morace, R.
Cantore, G.
Mirabella, G.
author_sort Mattia, M.
collection PubMed
description In humans, the ability to withhold manual motor responses seems to rely on a right-lateralized frontal–basal ganglia–thalamic network, including the pre-supplementary motor area and the inferior frontal gyrus (IFG). These areas should drive subthalamic nuclei to implement movement inhibition via the hyperdirect pathway. The output of this network is expected to influence those cortical areas underlying limb movement preparation and initiation, i.e., premotor (PMA) and primary motor (M1) cortices. Electroencephalographic (EEG) studies have shown an enhancement of the N200/P300 complex in the event-related potentials (ERPs) when a planned reaching movement is successfully stopped after the presentation of an infrequent stop-signal. PMA and M1 have been suggested as possible neural sources of this ERP complex but, due to the limited spatial resolution of scalp EEG, it is not yet clear which cortical areas contribute to its generation. To elucidate the role of motor cortices, we recorded epicortical ERPs from the lateral surface of the fronto-temporal lobes of five pharmacoresistant epileptic patients performing a reaching version of the countermanding task while undergoing presurgical monitoring. We consistently found a stereotyped ERP complex on a single-trial level when a movement was successfully cancelled. These ERPs were selectively expressed in M1, PMA, and Brodmann's area (BA) 9 and their onsets preceded the end of the stop process, suggesting a causal involvement in this executive function. Such ERPs also occurred in unsuccessful-stop (US) trials, that is, when subjects moved despite the occurrence of a stop-signal, mostly when they had long reaction times (RTs). These findings support the hypothesis that motor cortices are the final target of the inhibitory command elaborated by the frontal–basal ganglia–thalamic network.
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spelling pubmed-33865272012-07-02 Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements Mattia, M. Spadacenta, S. Pavone, L. Quarato, P. Esposito, V. Sparano, A. Sebastiano, F. Di Gennaro, G. Morace, R. Cantore, G. Mirabella, G. Front Neuroeng Neuroscience In humans, the ability to withhold manual motor responses seems to rely on a right-lateralized frontal–basal ganglia–thalamic network, including the pre-supplementary motor area and the inferior frontal gyrus (IFG). These areas should drive subthalamic nuclei to implement movement inhibition via the hyperdirect pathway. The output of this network is expected to influence those cortical areas underlying limb movement preparation and initiation, i.e., premotor (PMA) and primary motor (M1) cortices. Electroencephalographic (EEG) studies have shown an enhancement of the N200/P300 complex in the event-related potentials (ERPs) when a planned reaching movement is successfully stopped after the presentation of an infrequent stop-signal. PMA and M1 have been suggested as possible neural sources of this ERP complex but, due to the limited spatial resolution of scalp EEG, it is not yet clear which cortical areas contribute to its generation. To elucidate the role of motor cortices, we recorded epicortical ERPs from the lateral surface of the fronto-temporal lobes of five pharmacoresistant epileptic patients performing a reaching version of the countermanding task while undergoing presurgical monitoring. We consistently found a stereotyped ERP complex on a single-trial level when a movement was successfully cancelled. These ERPs were selectively expressed in M1, PMA, and Brodmann's area (BA) 9 and their onsets preceded the end of the stop process, suggesting a causal involvement in this executive function. Such ERPs also occurred in unsuccessful-stop (US) trials, that is, when subjects moved despite the occurrence of a stop-signal, mostly when they had long reaction times (RTs). These findings support the hypothesis that motor cortices are the final target of the inhibitory command elaborated by the frontal–basal ganglia–thalamic network. Frontiers Media S.A. 2012-06-29 /pmc/articles/PMC3386527/ /pubmed/22754525 http://dx.doi.org/10.3389/fneng.2012.00012 Text en Copyright © 2012 Mattia, Spadacenta, Pavone, Quarato, Esposito, Sparano, Sebastiano, Di Gennaro, Morace, Cantore and Mirabella. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
Mattia, M.
Spadacenta, S.
Pavone, L.
Quarato, P.
Esposito, V.
Sparano, A.
Sebastiano, F.
Di Gennaro, G.
Morace, R.
Cantore, G.
Mirabella, G.
Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
title Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
title_full Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
title_fullStr Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
title_full_unstemmed Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
title_short Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
title_sort stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386527/
https://www.ncbi.nlm.nih.gov/pubmed/22754525
http://dx.doi.org/10.3389/fneng.2012.00012
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