Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
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
_version_ 1783229885568778240
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
work_keys_str_mv AT kerrmatthewsd theroleofassociativecorticesandhippocampusduringmovementperturbations
AT sacrepierre theroleofassociativecorticesandhippocampusduringmovementperturbations
AT kahnkevin theroleofassociativecorticesandhippocampusduringmovementperturbations
AT parkhyunjoo theroleofassociativecorticesandhippocampusduringmovementperturbations
AT johnsonmathew theroleofassociativecorticesandhippocampusduringmovementperturbations
AT leejames theroleofassociativecorticesandhippocampusduringmovementperturbations
AT thompsonsusan theroleofassociativecorticesandhippocampusduringmovementperturbations
AT bulaciojuan theroleofassociativecorticesandhippocampusduringmovementperturbations
AT jonesjaes theroleofassociativecorticesandhippocampusduringmovementperturbations
AT gonzalezmartinezjorge theroleofassociativecorticesandhippocampusduringmovementperturbations
AT liegeoischauvelcatherine theroleofassociativecorticesandhippocampusduringmovementperturbations
AT sarmasrideviv theroleofassociativecorticesandhippocampusduringmovementperturbations
AT galejohnt theroleofassociativecorticesandhippocampusduringmovementperturbations
AT kerrmatthewsd roleofassociativecorticesandhippocampusduringmovementperturbations
AT sacrepierre roleofassociativecorticesandhippocampusduringmovementperturbations
AT kahnkevin roleofassociativecorticesandhippocampusduringmovementperturbations
AT parkhyunjoo roleofassociativecorticesandhippocampusduringmovementperturbations
AT johnsonmathew roleofassociativecorticesandhippocampusduringmovementperturbations
AT leejames roleofassociativecorticesandhippocampusduringmovementperturbations
AT thompsonsusan roleofassociativecorticesandhippocampusduringmovementperturbations
AT bulaciojuan roleofassociativecorticesandhippocampusduringmovementperturbations
AT jonesjaes roleofassociativecorticesandhippocampusduringmovementperturbations
AT gonzalezmartinezjorge roleofassociativecorticesandhippocampusduringmovementperturbations
AT liegeoischauvelcatherine roleofassociativecorticesandhippocampusduringmovementperturbations
AT sarmasrideviv roleofassociativecorticesandhippocampusduringmovementperturbations
AT galejohnt roleofassociativecorticesandhippocampusduringmovementperturbations