Cargando…

Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns

During behavior, the work done by actuators on the body can be resisted by the body's inertia, elastic forces, gravity, or viscosity. The dominant forces that resist actuation have major consequences on the control of that behavior. In the literature, features and actuation of locomotion, for e...

Descripción completa

Detalles Bibliográficos
Autores principales: Sutton, G P, Szczecinski, N S, Quinn, R D, Chiel, H J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563792/
https://www.ncbi.nlm.nih.gov/pubmed/37822766
http://dx.doi.org/10.1093/pnasnexus/pgad298
_version_ 1785118411256233984
author Sutton, G P
Szczecinski, N S
Quinn, R D
Chiel, H J
author_facet Sutton, G P
Szczecinski, N S
Quinn, R D
Chiel, H J
author_sort Sutton, G P
collection PubMed
description During behavior, the work done by actuators on the body can be resisted by the body's inertia, elastic forces, gravity, or viscosity. The dominant forces that resist actuation have major consequences on the control of that behavior. In the literature, features and actuation of locomotion, for example, have been successfully predicted by nondimensional numbers (e.g. Froude number and Reynolds number) that generally express the ratio between two of these forces (gravitational, inertial, elastic, and viscous). However, animals of different sizes or motions at different speeds may not share the same dominant forces within a behavior, making ratios of just two of these forces less useful. Thus, for a broad comparison of behavior across many orders of magnitude of limb length and cycle period, a dimensionless number that includes gravitational, inertial, elastic, and viscous forces is needed. This study proposes a nondimensional number that relates these four forces: the phase shift (ϕ) between the displacement of the limb and the actuator force that moves it. Using allometric scaling laws, ϕ for terrestrial walking is expressed as a function of the limb length and the cycle period at which the limb steps. Scale-dependent values of ϕ are used to explain and predict the electromyographic (EMG) patterns employed by different animals as they walk.
format Online
Article
Text
id pubmed-10563792
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-105637922023-10-11 Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns Sutton, G P Szczecinski, N S Quinn, R D Chiel, H J PNAS Nexus Biological, Health, and Medical Sciences During behavior, the work done by actuators on the body can be resisted by the body's inertia, elastic forces, gravity, or viscosity. The dominant forces that resist actuation have major consequences on the control of that behavior. In the literature, features and actuation of locomotion, for example, have been successfully predicted by nondimensional numbers (e.g. Froude number and Reynolds number) that generally express the ratio between two of these forces (gravitational, inertial, elastic, and viscous). However, animals of different sizes or motions at different speeds may not share the same dominant forces within a behavior, making ratios of just two of these forces less useful. Thus, for a broad comparison of behavior across many orders of magnitude of limb length and cycle period, a dimensionless number that includes gravitational, inertial, elastic, and viscous forces is needed. This study proposes a nondimensional number that relates these four forces: the phase shift (ϕ) between the displacement of the limb and the actuator force that moves it. Using allometric scaling laws, ϕ for terrestrial walking is expressed as a function of the limb length and the cycle period at which the limb steps. Scale-dependent values of ϕ are used to explain and predict the electromyographic (EMG) patterns employed by different animals as they walk. Oxford University Press 2023-10-10 /pmc/articles/PMC10563792/ /pubmed/37822766 http://dx.doi.org/10.1093/pnasnexus/pgad298 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of National Academy of Sciences. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (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 Biological, Health, and Medical Sciences
Sutton, G P
Szczecinski, N S
Quinn, R D
Chiel, H J
Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
title Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
title_full Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
title_fullStr Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
title_full_unstemmed Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
title_short Phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
title_sort phase shift between joint rotation and actuation reflects dominant forces and predicts muscle activation patterns
topic Biological, Health, and Medical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563792/
https://www.ncbi.nlm.nih.gov/pubmed/37822766
http://dx.doi.org/10.1093/pnasnexus/pgad298
work_keys_str_mv AT suttongp phaseshiftbetweenjointrotationandactuationreflectsdominantforcesandpredictsmuscleactivationpatterns
AT szczecinskins phaseshiftbetweenjointrotationandactuationreflectsdominantforcesandpredictsmuscleactivationpatterns
AT quinnrd phaseshiftbetweenjointrotationandactuationreflectsdominantforcesandpredictsmuscleactivationpatterns
AT chielhj phaseshiftbetweenjointrotationandactuationreflectsdominantforcesandpredictsmuscleactivationpatterns