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The Role of Associative Cortices and Hippocampus during Movement Perturbations
Although motor control has been extensively studied, most research involving neural recordings has focused on primary motor cortex, pre-motor cortex, supplementary motor area, and cerebellum. These regions are involved during normal movements, however, associative cortices and hippocampus are also l...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395558/ https://www.ncbi.nlm.nih.gov/pubmed/28469563 http://dx.doi.org/10.3389/fncir.2017.00026 |
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author | Kerr, Matthew S. D. Sacré, Pierre Kahn, Kevin Park, Hyun-Joo Johnson, Mathew Lee, James Thompson, Susan Bulacio, Juan Jones, Jaes González-Martínez, Jorge Liégeois-Chauvel, Catherine Sarma, Sridevi V. Gale, John T. |
author_facet | Kerr, Matthew S. D. Sacré, Pierre Kahn, Kevin Park, Hyun-Joo Johnson, Mathew Lee, James Thompson, Susan Bulacio, Juan Jones, Jaes González-Martínez, Jorge Liégeois-Chauvel, Catherine Sarma, Sridevi V. Gale, John T. |
author_sort | Kerr, Matthew S. D. |
collection | PubMed |
description | Although motor control has been extensively studied, most research involving neural recordings has focused on primary motor cortex, pre-motor cortex, supplementary motor area, and cerebellum. These regions are involved during normal movements, however, associative cortices and hippocampus are also likely involved during perturbed movements as one must detect the unexpected disturbance, inhibit the previous motor plan, and create a new plan to compensate. Minimal data is available on these brain regions during such “robust” movements. Here, epileptic patients implanted with intracerebral electrodes performed reaching movements while experiencing occasional unexpected force perturbations allowing study of the fronto-parietal, limbic and hippocampal network at unprecedented high spatial, and temporal scales. Areas including orbitofrontal cortex (OFC) and hippocampus showed increased activation during perturbed trials. These results, coupled with a visual novelty control task, suggest the hippocampal MTL-P300 novelty response is modality independent, and that the OFC is involved in modifying motor plans during robust movement. |
format | Online Article Text |
id | pubmed-5395558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53955582017-05-03 The Role of Associative Cortices and Hippocampus during Movement Perturbations Kerr, Matthew S. D. Sacré, Pierre Kahn, Kevin Park, Hyun-Joo Johnson, Mathew Lee, James Thompson, Susan Bulacio, Juan Jones, Jaes González-Martínez, Jorge Liégeois-Chauvel, Catherine Sarma, Sridevi V. Gale, John T. Front Neural Circuits Neuroscience Although motor control has been extensively studied, most research involving neural recordings has focused on primary motor cortex, pre-motor cortex, supplementary motor area, and cerebellum. These regions are involved during normal movements, however, associative cortices and hippocampus are also likely involved during perturbed movements as one must detect the unexpected disturbance, inhibit the previous motor plan, and create a new plan to compensate. Minimal data is available on these brain regions during such “robust” movements. Here, epileptic patients implanted with intracerebral electrodes performed reaching movements while experiencing occasional unexpected force perturbations allowing study of the fronto-parietal, limbic and hippocampal network at unprecedented high spatial, and temporal scales. Areas including orbitofrontal cortex (OFC) and hippocampus showed increased activation during perturbed trials. These results, coupled with a visual novelty control task, suggest the hippocampal MTL-P300 novelty response is modality independent, and that the OFC is involved in modifying motor plans during robust movement. Frontiers Media S.A. 2017-04-19 /pmc/articles/PMC5395558/ /pubmed/28469563 http://dx.doi.org/10.3389/fncir.2017.00026 Text en Copyright © 2017 Kerr, Sacré, Kahn, Park, Johnson, Lee, Thompson, Bulacio, Jones, González-Martínez, Liégeois-Chauvel, Sarma and Gale. http://creativecommons.org/licenses/by/4.0/ 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 Kerr, Matthew S. D. Sacré, Pierre Kahn, Kevin Park, Hyun-Joo Johnson, Mathew Lee, James Thompson, Susan Bulacio, Juan Jones, Jaes González-Martínez, Jorge Liégeois-Chauvel, Catherine Sarma, Sridevi V. Gale, John T. The Role of Associative Cortices and Hippocampus during Movement Perturbations |
title | The Role of Associative Cortices and Hippocampus during Movement Perturbations |
title_full | The Role of Associative Cortices and Hippocampus during Movement Perturbations |
title_fullStr | The Role of Associative Cortices and Hippocampus during Movement Perturbations |
title_full_unstemmed | The Role of Associative Cortices and Hippocampus during Movement Perturbations |
title_short | The Role of Associative Cortices and Hippocampus during Movement Perturbations |
title_sort | role of associative cortices and hippocampus during movement perturbations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395558/ https://www.ncbi.nlm.nih.gov/pubmed/28469563 http://dx.doi.org/10.3389/fncir.2017.00026 |
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