Cargando…

Skeletal muscle function underpins muscle spindle abundance

Muscle spindle abundance is highly variable within and across species, but we currently lack any clear picture of the mechanistic causes or consequences of this variation. Previous use of spindle abundance as a correlate for muscle function implies a mechanical underpinning to this variation, but th...

Descripción completa

Detalles Bibliográficos
Autores principales: Kissane, Roger W. P., Charles, James P., Banks, Robert W., Bates, Karl T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156921/
https://www.ncbi.nlm.nih.gov/pubmed/35642368
http://dx.doi.org/10.1098/rspb.2022.0622
_version_ 1784718537531588608
author Kissane, Roger W. P.
Charles, James P.
Banks, Robert W.
Bates, Karl T.
author_facet Kissane, Roger W. P.
Charles, James P.
Banks, Robert W.
Bates, Karl T.
author_sort Kissane, Roger W. P.
collection PubMed
description Muscle spindle abundance is highly variable within and across species, but we currently lack any clear picture of the mechanistic causes or consequences of this variation. Previous use of spindle abundance as a correlate for muscle function implies a mechanical underpinning to this variation, but these ideas have not been tested. Herein, we use integrated medical imaging and subject-specific musculoskeletal models to investigate the relationship between spindle abundance, muscle architecture and in vivo muscle behaviour in the human locomotor system. These analyses indicate that muscle spindle number is tightly correlated with muscle fascicle length, absolute fascicle length change, velocity of fibre lengthening and active muscle forces during walking. Novel correlations between functional indices and spindle abundance are also recovered, where muscles with a high abundance predominantly function as springs, compared to those with a lower abundance mostly functioning as brakes during walking. These data demonstrate that muscle fibre length, lengthening velocity and fibre force are key physiological signals to the central nervous system and its modulation of locomotion, and that muscle spindle abundance may be tightly correlated to how a muscle generates work. These insights may be combined with neuromechanics and robotic studies of motor control to help further tease apart the functional drivers of muscle spindle composition.
format Online
Article
Text
id pubmed-9156921
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-91569212022-06-13 Skeletal muscle function underpins muscle spindle abundance Kissane, Roger W. P. Charles, James P. Banks, Robert W. Bates, Karl T. Proc Biol Sci Morphology and Biomechanics Muscle spindle abundance is highly variable within and across species, but we currently lack any clear picture of the mechanistic causes or consequences of this variation. Previous use of spindle abundance as a correlate for muscle function implies a mechanical underpinning to this variation, but these ideas have not been tested. Herein, we use integrated medical imaging and subject-specific musculoskeletal models to investigate the relationship between spindle abundance, muscle architecture and in vivo muscle behaviour in the human locomotor system. These analyses indicate that muscle spindle number is tightly correlated with muscle fascicle length, absolute fascicle length change, velocity of fibre lengthening and active muscle forces during walking. Novel correlations between functional indices and spindle abundance are also recovered, where muscles with a high abundance predominantly function as springs, compared to those with a lower abundance mostly functioning as brakes during walking. These data demonstrate that muscle fibre length, lengthening velocity and fibre force are key physiological signals to the central nervous system and its modulation of locomotion, and that muscle spindle abundance may be tightly correlated to how a muscle generates work. These insights may be combined with neuromechanics and robotic studies of motor control to help further tease apart the functional drivers of muscle spindle composition. The Royal Society 2022-06-08 2022-06-01 /pmc/articles/PMC9156921/ /pubmed/35642368 http://dx.doi.org/10.1098/rspb.2022.0622 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society 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 use, provided the original author and source are credited.
spellingShingle Morphology and Biomechanics
Kissane, Roger W. P.
Charles, James P.
Banks, Robert W.
Bates, Karl T.
Skeletal muscle function underpins muscle spindle abundance
title Skeletal muscle function underpins muscle spindle abundance
title_full Skeletal muscle function underpins muscle spindle abundance
title_fullStr Skeletal muscle function underpins muscle spindle abundance
title_full_unstemmed Skeletal muscle function underpins muscle spindle abundance
title_short Skeletal muscle function underpins muscle spindle abundance
title_sort skeletal muscle function underpins muscle spindle abundance
topic Morphology and Biomechanics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156921/
https://www.ncbi.nlm.nih.gov/pubmed/35642368
http://dx.doi.org/10.1098/rspb.2022.0622
work_keys_str_mv AT kissanerogerwp skeletalmusclefunctionunderpinsmusclespindleabundance
AT charlesjamesp skeletalmusclefunctionunderpinsmusclespindleabundance
AT banksrobertw skeletalmusclefunctionunderpinsmusclespindleabundance
AT bateskarlt skeletalmusclefunctionunderpinsmusclespindleabundance