Cargando…

A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans

Evolution of the direct, monosynaptic connection from the primary motor cortex to the spinal cord parallels acquisition of hand dexterity and lateralization of hand preference. In non-human mammals, the indirect, multi-synaptic connections between the bilateral primary motor cortices and the spinal...

Descripción completa

Detalles Bibliográficos
Autores principales: Takasawa, Eiji, Abe, Mitsunari, Chikuda, Hirotaka, Hanakawa, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256686/
https://www.ncbi.nlm.nih.gov/pubmed/35790815
http://dx.doi.org/10.1038/s42003-022-03615-2
_version_ 1784741185831567360
author Takasawa, Eiji
Abe, Mitsunari
Chikuda, Hirotaka
Hanakawa, Takashi
author_facet Takasawa, Eiji
Abe, Mitsunari
Chikuda, Hirotaka
Hanakawa, Takashi
author_sort Takasawa, Eiji
collection PubMed
description Evolution of the direct, monosynaptic connection from the primary motor cortex to the spinal cord parallels acquisition of hand dexterity and lateralization of hand preference. In non-human mammals, the indirect, multi-synaptic connections between the bilateral primary motor cortices and the spinal cord also participates in controlling dexterous hand movement. However, it remains unknown how the direct and indirect corticospinal pathways work in concert to control unilateral hand movement with lateralized preference in humans. Here we demonstrated the asymmetric functional organization of the two corticospinal networks, by combining network modelling and simultaneous functional magnetic resonance imaging techniques of the brain and the spinal cord. Moreover, we also found that the degree of the involvement of the two corticospinal networks paralleled lateralization of hand preference. The present results pointed to the functionally lateralized motor nervous system that underlies the behavioral asymmetry of handedness in humans.
format Online
Article
Text
id pubmed-9256686
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-92566862022-07-07 A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans Takasawa, Eiji Abe, Mitsunari Chikuda, Hirotaka Hanakawa, Takashi Commun Biol Article Evolution of the direct, monosynaptic connection from the primary motor cortex to the spinal cord parallels acquisition of hand dexterity and lateralization of hand preference. In non-human mammals, the indirect, multi-synaptic connections between the bilateral primary motor cortices and the spinal cord also participates in controlling dexterous hand movement. However, it remains unknown how the direct and indirect corticospinal pathways work in concert to control unilateral hand movement with lateralized preference in humans. Here we demonstrated the asymmetric functional organization of the two corticospinal networks, by combining network modelling and simultaneous functional magnetic resonance imaging techniques of the brain and the spinal cord. Moreover, we also found that the degree of the involvement of the two corticospinal networks paralleled lateralization of hand preference. The present results pointed to the functionally lateralized motor nervous system that underlies the behavioral asymmetry of handedness in humans. Nature Publishing Group UK 2022-07-05 /pmc/articles/PMC9256686/ /pubmed/35790815 http://dx.doi.org/10.1038/s42003-022-03615-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Takasawa, Eiji
Abe, Mitsunari
Chikuda, Hirotaka
Hanakawa, Takashi
A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans
title A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans
title_full A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans
title_fullStr A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans
title_full_unstemmed A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans
title_short A computational model based on corticospinal functional MRI revealed asymmetrically organized motor corticospinal networks in humans
title_sort computational model based on corticospinal functional mri revealed asymmetrically organized motor corticospinal networks in humans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256686/
https://www.ncbi.nlm.nih.gov/pubmed/35790815
http://dx.doi.org/10.1038/s42003-022-03615-2
work_keys_str_mv AT takasawaeiji acomputationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT abemitsunari acomputationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT chikudahirotaka acomputationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT hanakawatakashi acomputationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT takasawaeiji computationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT abemitsunari computationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT chikudahirotaka computationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans
AT hanakawatakashi computationalmodelbasedoncorticospinalfunctionalmrirevealedasymmetricallyorganizedmotorcorticospinalnetworksinhumans