Cargando…
Forelimb force direction and magnitude independently controlled by spinal modules in the macaque
Modular organization of the spinal motor system is thought to reduce the cognitive complexity of simultaneously controlling the large number of muscles and joints in the human body. Although modular organization has been confirmed in the hindlimb control system of several animal species, it has yet...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959559/ https://www.ncbi.nlm.nih.gov/pubmed/33060294 http://dx.doi.org/10.1073/pnas.1919253117 |
_version_ | 1783664978806439936 |
---|---|
author | Yaron, Amit Kowalski, David Yaguchi, Hiroaki Takei, Tomohiko Seki, Kazuhiko |
author_facet | Yaron, Amit Kowalski, David Yaguchi, Hiroaki Takei, Tomohiko Seki, Kazuhiko |
author_sort | Yaron, Amit |
collection | PubMed |
description | Modular organization of the spinal motor system is thought to reduce the cognitive complexity of simultaneously controlling the large number of muscles and joints in the human body. Although modular organization has been confirmed in the hindlimb control system of several animal species, it has yet to be established in the forelimb motor system or in primates. Expanding upon experiments originally performed in the frog lumbar spinal cord, we examined whether costimulation of two sites in the macaque monkey cervical spinal cord results in motor activity that is a simple linear sum of the responses evoked by stimulating each site individually. Similar to previous observations in the frog and rodent hindlimb, our analysis revealed that in most cases (77% of all pairs) the directions of the force fields elicited by costimulation were highly similar to those predicted by the simple linear sum of those elicited by stimulating each site individually. A comparable simple summation of electromyography (EMG) output, especially in the proximal muscles, suggested that this linear summation of force field direction was produced by a spinal neural mechanism whereby the forelimb motor output recruited by costimulation was also summed linearly. We further found that the force field magnitudes exhibited supralinear (amplified) summation, which was also observed in the EMG output of distal forelimb muscles, implying a novel feature of primate forelimb control. Overall, our observations support the idea that complex movements in the primate forelimb control system are made possible by flexibly combined spinal motor modules. |
format | Online Article Text |
id | pubmed-7959559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-79595592021-03-23 Forelimb force direction and magnitude independently controlled by spinal modules in the macaque Yaron, Amit Kowalski, David Yaguchi, Hiroaki Takei, Tomohiko Seki, Kazuhiko Proc Natl Acad Sci U S A Biological Sciences Modular organization of the spinal motor system is thought to reduce the cognitive complexity of simultaneously controlling the large number of muscles and joints in the human body. Although modular organization has been confirmed in the hindlimb control system of several animal species, it has yet to be established in the forelimb motor system or in primates. Expanding upon experiments originally performed in the frog lumbar spinal cord, we examined whether costimulation of two sites in the macaque monkey cervical spinal cord results in motor activity that is a simple linear sum of the responses evoked by stimulating each site individually. Similar to previous observations in the frog and rodent hindlimb, our analysis revealed that in most cases (77% of all pairs) the directions of the force fields elicited by costimulation were highly similar to those predicted by the simple linear sum of those elicited by stimulating each site individually. A comparable simple summation of electromyography (EMG) output, especially in the proximal muscles, suggested that this linear summation of force field direction was produced by a spinal neural mechanism whereby the forelimb motor output recruited by costimulation was also summed linearly. We further found that the force field magnitudes exhibited supralinear (amplified) summation, which was also observed in the EMG output of distal forelimb muscles, implying a novel feature of primate forelimb control. Overall, our observations support the idea that complex movements in the primate forelimb control system are made possible by flexibly combined spinal motor modules. National Academy of Sciences 2020-11-03 2020-10-15 /pmc/articles/PMC7959559/ /pubmed/33060294 http://dx.doi.org/10.1073/pnas.1919253117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Yaron, Amit Kowalski, David Yaguchi, Hiroaki Takei, Tomohiko Seki, Kazuhiko Forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
title | Forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
title_full | Forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
title_fullStr | Forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
title_full_unstemmed | Forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
title_short | Forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
title_sort | forelimb force direction and magnitude independently controlled by spinal modules in the macaque |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959559/ https://www.ncbi.nlm.nih.gov/pubmed/33060294 http://dx.doi.org/10.1073/pnas.1919253117 |
work_keys_str_mv | AT yaronamit forelimbforcedirectionandmagnitudeindependentlycontrolledbyspinalmodulesinthemacaque AT kowalskidavid forelimbforcedirectionandmagnitudeindependentlycontrolledbyspinalmodulesinthemacaque AT yaguchihiroaki forelimbforcedirectionandmagnitudeindependentlycontrolledbyspinalmodulesinthemacaque AT takeitomohiko forelimbforcedirectionandmagnitudeindependentlycontrolledbyspinalmodulesinthemacaque AT sekikazuhiko forelimbforcedirectionandmagnitudeindependentlycontrolledbyspinalmodulesinthemacaque |