Cargando…

Learning to stand with unexpected sensorimotor delays

Human standing balance relies on self-motion estimates that are used by the nervous system to detect unexpected movements and enable corrective responses and adaptations in control. These estimates must accommodate for inherent delays in sensory and motor pathways. Here, we used a robotic system to...

Descripción completa

Detalles Bibliográficos
Autores principales: Rasman, Brandon G, Forbes, Patrick A, Peters, Ryan M, Ortiz, Oscar, Franks, Ian, Inglis, J Timothy, Chua, Romeo, Blouin, Jean-Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480973/
https://www.ncbi.nlm.nih.gov/pubmed/34374648
http://dx.doi.org/10.7554/eLife.65085
_version_ 1784576581173248000
author Rasman, Brandon G
Forbes, Patrick A
Peters, Ryan M
Ortiz, Oscar
Franks, Ian
Inglis, J Timothy
Chua, Romeo
Blouin, Jean-Sébastien
author_facet Rasman, Brandon G
Forbes, Patrick A
Peters, Ryan M
Ortiz, Oscar
Franks, Ian
Inglis, J Timothy
Chua, Romeo
Blouin, Jean-Sébastien
author_sort Rasman, Brandon G
collection PubMed
description Human standing balance relies on self-motion estimates that are used by the nervous system to detect unexpected movements and enable corrective responses and adaptations in control. These estimates must accommodate for inherent delays in sensory and motor pathways. Here, we used a robotic system to simulate human standing about the ankles in the anteroposterior direction and impose sensorimotor delays into the control of balance. Imposed delays destabilized standing, but through training, participants adapted and re-learned to balance with the delays. Before training, imposed delays attenuated vestibular contributions to balance and triggered perceptions of unexpected standing motion, suggesting increased uncertainty in the internal self-motion estimates. After training, vestibular contributions partially returned to baseline levels and larger delays were needed to evoke perceptions of unexpected standing motion. Through learning, the nervous system accommodates balance sensorimotor delays by causally linking whole-body sensory feedback (initially interpreted as imposed motion) to self-generated balance motor commands.
format Online
Article
Text
id pubmed-8480973
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-84809732021-09-30 Learning to stand with unexpected sensorimotor delays Rasman, Brandon G Forbes, Patrick A Peters, Ryan M Ortiz, Oscar Franks, Ian Inglis, J Timothy Chua, Romeo Blouin, Jean-Sébastien eLife Neuroscience Human standing balance relies on self-motion estimates that are used by the nervous system to detect unexpected movements and enable corrective responses and adaptations in control. These estimates must accommodate for inherent delays in sensory and motor pathways. Here, we used a robotic system to simulate human standing about the ankles in the anteroposterior direction and impose sensorimotor delays into the control of balance. Imposed delays destabilized standing, but through training, participants adapted and re-learned to balance with the delays. Before training, imposed delays attenuated vestibular contributions to balance and triggered perceptions of unexpected standing motion, suggesting increased uncertainty in the internal self-motion estimates. After training, vestibular contributions partially returned to baseline levels and larger delays were needed to evoke perceptions of unexpected standing motion. Through learning, the nervous system accommodates balance sensorimotor delays by causally linking whole-body sensory feedback (initially interpreted as imposed motion) to self-generated balance motor commands. eLife Sciences Publications, Ltd 2021-08-10 /pmc/articles/PMC8480973/ /pubmed/34374648 http://dx.doi.org/10.7554/eLife.65085 Text en © 2021, Rasman et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Rasman, Brandon G
Forbes, Patrick A
Peters, Ryan M
Ortiz, Oscar
Franks, Ian
Inglis, J Timothy
Chua, Romeo
Blouin, Jean-Sébastien
Learning to stand with unexpected sensorimotor delays
title Learning to stand with unexpected sensorimotor delays
title_full Learning to stand with unexpected sensorimotor delays
title_fullStr Learning to stand with unexpected sensorimotor delays
title_full_unstemmed Learning to stand with unexpected sensorimotor delays
title_short Learning to stand with unexpected sensorimotor delays
title_sort learning to stand with unexpected sensorimotor delays
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480973/
https://www.ncbi.nlm.nih.gov/pubmed/34374648
http://dx.doi.org/10.7554/eLife.65085
work_keys_str_mv AT rasmanbrandong learningtostandwithunexpectedsensorimotordelays
AT forbespatricka learningtostandwithunexpectedsensorimotordelays
AT petersryanm learningtostandwithunexpectedsensorimotordelays
AT ortizoscar learningtostandwithunexpectedsensorimotordelays
AT franksian learningtostandwithunexpectedsensorimotordelays
AT inglisjtimothy learningtostandwithunexpectedsensorimotordelays
AT chuaromeo learningtostandwithunexpectedsensorimotordelays
AT blouinjeansebastien learningtostandwithunexpectedsensorimotordelays