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...

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Main Authors: Brandon G Rasman, Patrick A Forbes, Ryan M Peters, Oscar Ortiz, Ian Franks, J Timothy Inglis, Romeo Chua, Jean-Sébastien Blouin
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-08-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/65085
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author Brandon G Rasman
Patrick A Forbes
Ryan M Peters
Oscar Ortiz
Ian Franks
J Timothy Inglis
Romeo Chua
Jean-Sébastien Blouin
author_facet Brandon G Rasman
Patrick A Forbes
Ryan M Peters
Oscar Ortiz
Ian Franks
J Timothy Inglis
Romeo Chua
Jean-Sébastien Blouin
author_sort Brandon G Rasman
collection DOAJ
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.
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spelling doaj.art-e87ae73a3b0a49598fd891b5ef4465612022-12-22T02:05:16ZengeLife Sciences Publications LtdeLife2050-084X2021-08-011010.7554/eLife.65085Learning to stand with unexpected sensorimotor delaysBrandon G Rasman0https://orcid.org/0000-0002-8031-8320Patrick A Forbes1https://orcid.org/0000-0002-0230-9971Ryan M Peters2Oscar Ortiz3Ian Franks4J Timothy Inglis5Romeo Chua6Jean-Sébastien Blouin7https://orcid.org/0000-0003-0046-4051School of Physical Education, Sport, and Exercise Sciences, University of Otago, Dunedin, New Zealand; Department of Neuroscience, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands; School of Kinesiology, University of British Columbia, Vancouver, CanadaDepartment of Neuroscience, Erasmus MC, University Medical Center Rotterdam, Rotterdam, NetherlandsSchool of Kinesiology, University of British Columbia, Vancouver, Canada; Faculty of Kinesiology, University of Calgary, Calgary, Canada; Hotchkiss Brain Institute, Calgary, CanadaSchool of Kinesiology, University of British Columbia, Vancouver, Canada; Faculty of Kinesiology, University of New Brunswick, Fredericton, CanadaSchool of Kinesiology, University of British Columbia, Vancouver, CanadaSchool of Kinesiology, University of British Columbia, Vancouver, Canada; Djavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, CanadaSchool of Kinesiology, University of British Columbia, Vancouver, CanadaSchool of Kinesiology, University of British Columbia, Vancouver, Canada; Djavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, Canada; Institute for Computing, Information and Cognitive Systems, University of British Columbia, Vancouver, CanadaHuman 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.https://elifesciences.org/articles/65085sensorimotor delaysensorimotor adaptationstanding balance controlvestibularmotion perceptionposture
spellingShingle Brandon G Rasman
Patrick A Forbes
Ryan M Peters
Oscar Ortiz
Ian Franks
J Timothy Inglis
Romeo Chua
Jean-Sébastien Blouin
Learning to stand with unexpected sensorimotor delays
eLife
sensorimotor delay
sensorimotor adaptation
standing balance control
vestibular
motion perception
posture
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 sensorimotor delay
sensorimotor adaptation
standing balance control
vestibular
motion perception
posture
url https://elifesciences.org/articles/65085
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