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Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex

The organizing principle of human motor cortex does not follow an anatomical body map, but rather a distributed representational structure in which motor primitives are combined to produce motor outputs. Electrophysiological recordings in primates and human imaging data suggest that M1 encodes kinem...

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Autores principales: Kolasinski, James, Dima, Diana C, Mehler, David M A, Stephenson, Alice, Valadan, Sara, Kusmia, Slawomir, Rossiter, Holly E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446240/
https://www.ncbi.nlm.nih.gov/pubmed/32864612
http://dx.doi.org/10.1093/texcom/tgaa009
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author Kolasinski, James
Dima, Diana C
Mehler, David M A
Stephenson, Alice
Valadan, Sara
Kusmia, Slawomir
Rossiter, Holly E
author_facet Kolasinski, James
Dima, Diana C
Mehler, David M A
Stephenson, Alice
Valadan, Sara
Kusmia, Slawomir
Rossiter, Holly E
author_sort Kolasinski, James
collection PubMed
description The organizing principle of human motor cortex does not follow an anatomical body map, but rather a distributed representational structure in which motor primitives are combined to produce motor outputs. Electrophysiological recordings in primates and human imaging data suggest that M1 encodes kinematic features of movements, such as joint position and velocity. However, M1 exhibits well-documented sensory responses to cutaneous and proprioceptive stimuli, raising questions regarding the origins of kinematic motor representations: are they relevant in top-down motor control, or are they an epiphenomenon of bottom-up sensory feedback during movement? Here we provide evidence for spatially and temporally distinct encoding of kinematic and muscle information in human M1 during the production of a wide variety of naturalistic hand movements. Using a powerful combination of high-field functional magnetic resonance imaging and magnetoencephalography, a spatial and temporal multivariate representational similarity analysis revealed encoding of kinematic information in more caudal regions of M1, over 200 ms before movement onset. In contrast, patterns of muscle activity were encoded in more rostral motor regions much later after movements began. We provide compelling evidence that top-down control of dexterous movement engages kinematic representations in caudal regions of M1 prior to movement production.
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spelling pubmed-74462402020-08-27 Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex Kolasinski, James Dima, Diana C Mehler, David M A Stephenson, Alice Valadan, Sara Kusmia, Slawomir Rossiter, Holly E Cereb Cortex Commun Original Article The organizing principle of human motor cortex does not follow an anatomical body map, but rather a distributed representational structure in which motor primitives are combined to produce motor outputs. Electrophysiological recordings in primates and human imaging data suggest that M1 encodes kinematic features of movements, such as joint position and velocity. However, M1 exhibits well-documented sensory responses to cutaneous and proprioceptive stimuli, raising questions regarding the origins of kinematic motor representations: are they relevant in top-down motor control, or are they an epiphenomenon of bottom-up sensory feedback during movement? Here we provide evidence for spatially and temporally distinct encoding of kinematic and muscle information in human M1 during the production of a wide variety of naturalistic hand movements. Using a powerful combination of high-field functional magnetic resonance imaging and magnetoencephalography, a spatial and temporal multivariate representational similarity analysis revealed encoding of kinematic information in more caudal regions of M1, over 200 ms before movement onset. In contrast, patterns of muscle activity were encoded in more rostral motor regions much later after movements began. We provide compelling evidence that top-down control of dexterous movement engages kinematic representations in caudal regions of M1 prior to movement production. Oxford University Press 2020-04-04 /pmc/articles/PMC7446240/ /pubmed/32864612 http://dx.doi.org/10.1093/texcom/tgaa009 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kolasinski, James
Dima, Diana C
Mehler, David M A
Stephenson, Alice
Valadan, Sara
Kusmia, Slawomir
Rossiter, Holly E
Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex
title Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex
title_full Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex
title_fullStr Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex
title_full_unstemmed Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex
title_short Spatially and Temporally Distinct Encoding of Muscle and Kinematic Information in Rostral and Caudal Primary Motor Cortex
title_sort spatially and temporally distinct encoding of muscle and kinematic information in rostral and caudal primary motor cortex
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446240/
https://www.ncbi.nlm.nih.gov/pubmed/32864612
http://dx.doi.org/10.1093/texcom/tgaa009
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