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Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli

Control of adaptive walking requires the integration of sensory signals of muscle force and load. We have studied how mechanoreceptors (tibial campaniform sensilla) encode “naturalistic” stimuli derived from joint torques of stick insects walking on a horizontal substrate. Previous studies showed th...

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Autores principales: Zill, Sasha N., Dallmann, Chris J., S. Szczecinski, Nicholas, Büschges, Ansgar, Schmitz, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424542/
https://www.ncbi.nlm.nih.gov/pubmed/34107221
http://dx.doi.org/10.1152/jn.00120.2021
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author Zill, Sasha N.
Dallmann, Chris J.
S. Szczecinski, Nicholas
Büschges, Ansgar
Schmitz, Josef
author_facet Zill, Sasha N.
Dallmann, Chris J.
S. Szczecinski, Nicholas
Büschges, Ansgar
Schmitz, Josef
author_sort Zill, Sasha N.
collection PubMed
description Control of adaptive walking requires the integration of sensory signals of muscle force and load. We have studied how mechanoreceptors (tibial campaniform sensilla) encode “naturalistic” stimuli derived from joint torques of stick insects walking on a horizontal substrate. Previous studies showed that forces applied to the legs using the mean torque profiles of a proximal joint were highly effective in eliciting motor activities. However, substantial variations in torque direction and magnitude occurred at the more distal femorotibial joint, which can generate braking or propulsive forces and provide lateral stability. To determine how these forces are encoded, we used torque waveforms of individual steps that had maximum values in stance in the directions of flexion or extension. Analysis of kinematic data showed that the torques in different directions tended to occur in different ranges of joint angles. Variations within stance were not accompanied by comparable changes in joint angle but often reflected vertical ground reaction forces and leg support of body load. Application of torque waveforms elicited sensory discharges with variations in firing frequency similar to those seen in freely walking insects. All sensilla directionally encoded the dynamics of force increases and showed hysteresis to transient force decreases. Smaller receptors exhibited more tonic firing. Our findings suggest that dynamic sensitivity in force feedback can modulate ongoing muscle activities to stabilize distal joints when large forces are generated at proximal joints. Furthermore, use of “naturalistic” stimuli can reproduce characteristics seen in freely moving animals that are absent in conventional restrained preparations. NEW & NOTEWORTHY Sensory encoding of forces during walking by campaniform sensilla was characterized in stick insects using waveforms of joint torques calculated by inverse dynamics as mechanical stimuli. Tests using the mean joint torque and torques of individual steps showed the system is highly sensitive to force dynamics (dF/dt). Use of “naturalistic” stimuli can reproduce characteristics of sensory discharges seen in freely walking insects, such as load transfer among legs.
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spelling pubmed-84245422022-07-01 Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli Zill, Sasha N. Dallmann, Chris J. S. Szczecinski, Nicholas Büschges, Ansgar Schmitz, Josef J Neurophysiol Research Article Control of adaptive walking requires the integration of sensory signals of muscle force and load. We have studied how mechanoreceptors (tibial campaniform sensilla) encode “naturalistic” stimuli derived from joint torques of stick insects walking on a horizontal substrate. Previous studies showed that forces applied to the legs using the mean torque profiles of a proximal joint were highly effective in eliciting motor activities. However, substantial variations in torque direction and magnitude occurred at the more distal femorotibial joint, which can generate braking or propulsive forces and provide lateral stability. To determine how these forces are encoded, we used torque waveforms of individual steps that had maximum values in stance in the directions of flexion or extension. Analysis of kinematic data showed that the torques in different directions tended to occur in different ranges of joint angles. Variations within stance were not accompanied by comparable changes in joint angle but often reflected vertical ground reaction forces and leg support of body load. Application of torque waveforms elicited sensory discharges with variations in firing frequency similar to those seen in freely walking insects. All sensilla directionally encoded the dynamics of force increases and showed hysteresis to transient force decreases. Smaller receptors exhibited more tonic firing. Our findings suggest that dynamic sensitivity in force feedback can modulate ongoing muscle activities to stabilize distal joints when large forces are generated at proximal joints. Furthermore, use of “naturalistic” stimuli can reproduce characteristics seen in freely moving animals that are absent in conventional restrained preparations. NEW & NOTEWORTHY Sensory encoding of forces during walking by campaniform sensilla was characterized in stick insects using waveforms of joint torques calculated by inverse dynamics as mechanical stimuli. Tests using the mean joint torque and torques of individual steps showed the system is highly sensitive to force dynamics (dF/dt). Use of “naturalistic” stimuli can reproduce characteristics of sensory discharges seen in freely walking insects, such as load transfer among legs. American Physiological Society 2021-07-01 2021-06-09 /pmc/articles/PMC8424542/ /pubmed/34107221 http://dx.doi.org/10.1152/jn.00120.2021 Text en Copyright © 2021 The Authors https://creativecommons.org/licenses/by/4.0/Licensed under Creative Commons Attribution CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/) . Published by the American Physiological Society.
spellingShingle Research Article
Zill, Sasha N.
Dallmann, Chris J.
S. Szczecinski, Nicholas
Büschges, Ansgar
Schmitz, Josef
Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
title Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
title_full Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
title_fullStr Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
title_full_unstemmed Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
title_short Evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
title_sort evaluation of force feedback in walking using joint torques as “naturalistic” stimuli
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424542/
https://www.ncbi.nlm.nih.gov/pubmed/34107221
http://dx.doi.org/10.1152/jn.00120.2021
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