Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE

User menu

  • Log out
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • Log out
  • Log in
  • My Cart
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE
PreviousNext
Featured ArticleResearch Articles, Systems/Circuits

The Volitional Control of Individual Motor Units Is Constrained within Low-Dimensional Neural Manifolds by Common Inputs

Julien Rossato, Simon Avrillon, Kylie Tucker, Dario Farina and François Hug
Journal of Neuroscience 21 August 2024, 44 (34) e0702242024; https://doi.org/10.1523/JNEUROSCI.0702-24.2024
Julien Rossato
1Laboratory “Movement, Interactions, Performance” (UR 4334), Nantes Université, Nantes, France
2Laboratory of Neuromotor Physiology, IRCCS Fondazione Santa Lucia, Rome, Italy
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Simon Avrillon
3Department of Bioengineering, Faculty of Engineering, Imperial College London, London, United Kingdom
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Simon Avrillon
Kylie Tucker
4School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Dario Farina
3Department of Bioengineering, Faculty of Engineering, Imperial College London, London, United Kingdom
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Dario Farina
François Hug
4School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia
5LAMHESS, Université Côte d'Azur, Nice, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for François Hug
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • Peer Review
  • PDF
Loading

Article Figures & Data

Figures

  • Figure 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 1.

    Experimental setup and protocol. A, Participants performed submaximal isometric plantar flexions or knee extensions. Electromyographic signals were recorded using grids of surface electrodes and decomposed into motor unit discharge times. We used an online feedback motor unit (MU) control paradigm to test the hypothesis that the central nervous system mainly adopts a rigid control of the motor units during a single-joint task. B, Participants first performed a series of 10 contractions with torque feedback (reference contractions, B). In the second part of the experiment, motor unit firing rates were estimated in real time and converted into visual feedback displayed to the participant (online control contractions, C). The visual feedback consisted of a two-dimensional space in which a cursor moved according to the firing rates of two motor units. Two targets (Target 1 and Target 2) were alternately displayed to the participant, who had to differentially modulate the firing rates of the two motor units to alternately move the cursor toward one of the two targets. B, The firing rates of the motor unit 1 from the gastrocnemius lateralis (GL) and motor unit 7 from the gastrocnemius medialis (GM) of one participant are displayed across the 10 trials. Note that the two-dimensional space is displayed in panel B but was not provided as feedback to the participants during the reference contractions. This example shows a clear dissociation of the activity of two motor units from different muscles, i.e., GL and GM, during the online control task. Such a dissociation was not observed for GM–GM and vastus lateralis–vastus medialis motor units.

  • Figure 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 2.

    Motor unit behavior during the reference contractions. A, Biplots in which the coordinates of each motor unit represent its weights within the two latent factors, as identified using non-negative matrix factorization (data depicted for three participants: P3, P5, and P14). Angles between vectors were calculated to estimate the level of common inputs for each pair of motor unit. It is worth noting that the firing activity of GL–GM motor units was either well correlated (P5) or uncorrelated (P3), while the firing activity of VL–VM motor units systematically covaried (P14). B, Results are displayed for all participants, where each gray dot represents a pair of motor units and each colored dot represents a pair that was used as feedback in the second part of the experiment. The box denotes the 25th and 75th percentiles of the values distribution. The line is the median. The thick horizontal black lines denote a significant statistical difference between muscles (p < 0.05).

  • Figure 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 3.

    Volitional control of motor unit firing rates. A, Typical examples of cursor positions are depicted for the 10 reference contractions (only torque feedback) and the online contractions (5 for each target). The success rate is displayed for each target. It is calculated as the percentage of time spent within the target (while maintaining the torque constant) over the total duration of the trial. B, Relation between the angle between motor units estimated from the reference contractions and the success rate in Target 2 (true flexible control) for all the displayed motor units. Each data point is a pair of motor units, and the color code is the same as in C. C, Success rate for Targets 1 (T1) and 2 (T2). Each data point is a pair of motor units, the box denotes the 25th and 75th percentiles of the distribution of scores, and the line is the median. The thick horizontal black lines denote a significant statistical difference between muscles (p < 0.05).

  • Figure 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 4.

    Changes in firing rate at the motor unit population level. A, We calculated the correlation coefficients between the smoothed firing rates of the motor units displayed to the participant and the smoothed firing rates of the nondisplayed units. In this example, the correlation coefficient between the firing rates of the two displayed motor units was 0.01 (left panel), showing a perfect dissociation of the activity of the two units. We extended the analysis to the correlation between the firing rate of the displayed motor units from the GL (central panel) or GM (right panel) and all the other motor units from GM. Each pair of motor units has a different color. B, Correlation coefficients between the motor units (displayed and nondisplayed to the participants) during the reference contractions and the online control contractions. Each data point is a pair of motor units, and the connecting line denotes the change in correlation between conditions. The box denotes the 25th and 75th percentiles of the distribution of coefficients, and the black line is the median. The thick horizontal black lines represent a significant statistical difference between conditions. C, The changes in correlations observed between reference contractions and online control trials were separated between all pairs of motor units displayed to the participant (top panel). The changes in correlations between the displayed units and those nondisplayed units are shown in the bottom panel.

  • Figure 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 5.

    Control strategies during the online task. A, To investigate the strategies associated with the dissociation of GL and GM motor unit firing rates, we identified the time stamps where the cursor was in the target favoring GL (TGL) or GM (TGM) motor unit recruitment. TGas refers to a cursor position between the two targets. Ankle moments and EMG amplitudes of the tibialis anterior and vastus lateralis were averaged over these periods and compared. B, Average ankle force moments during the reference (Ref) contractions and the three targets. Each data point is a participant and the connect lines denote the variations between conditions. The box represents the 25th and 75th percentiles of the distribution of moments and the black line is the median. C, Each data point is a participant and the connecting lines denote the variations between conditions. The box represents the 25th and 75th percentiles of the distribution of EMG amplitudes and the black line is the median. The thick horizontal black lines represent a significant statistical difference between conditions (p < 0.05).

Back to top

In this issue

The Journal of Neuroscience: 44 (34)
Journal of Neuroscience
Vol. 44, Issue 34
21 Aug 2024
  • Table of Contents
  • About the Cover
  • Index by author
  • Masthead (PDF)
Email

Thank you for sharing this Journal of Neuroscience article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
The Volitional Control of Individual Motor Units Is Constrained within Low-Dimensional Neural Manifolds by Common Inputs
(Your Name) has forwarded a page to you from Journal of Neuroscience
(Your Name) thought you would be interested in this article in Journal of Neuroscience.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Citation Tools
The Volitional Control of Individual Motor Units Is Constrained within Low-Dimensional Neural Manifolds by Common Inputs
Julien Rossato, Simon Avrillon, Kylie Tucker, Dario Farina, François Hug
Journal of Neuroscience 21 August 2024, 44 (34) e0702242024; DOI: 10.1523/JNEUROSCI.0702-24.2024

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Request Permissions
Share
The Volitional Control of Individual Motor Units Is Constrained within Low-Dimensional Neural Manifolds by Common Inputs
Julien Rossato, Simon Avrillon, Kylie Tucker, Dario Farina, François Hug
Journal of Neuroscience 21 August 2024, 44 (34) e0702242024; DOI: 10.1523/JNEUROSCI.0702-24.2024
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Significance Statement
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Data Availability
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • eLetters
  • Peer Review
  • PDF

Keywords

  • electromyography
  • module
  • motor neuron
  • real-time feedback
  • synergy

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

Research Articles

  • Increased perceptual reliability reduces membrane potential variability in cortical neurons
  • Synergistic geniculate and cortical dynamics facilitate a decorrelated spatial frequency code in the early visual system
  • Is the whole the sum of its parts? Neural computation of consumer bundle valuation in humans
Show more Research Articles

Systems/Circuits

  • Increased perceptual reliability reduces membrane potential variability in cortical neurons
  • Synergistic geniculate and cortical dynamics facilitate a decorrelated spatial frequency code in the early visual system
  • Is the whole the sum of its parts? Neural computation of consumer bundle valuation in humans
Show more Systems/Circuits
  • Home
  • Alerts
  • Follow SFN on BlueSky
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Issue Archive
  • Collections

Information

  • For Authors
  • For Advertisers
  • For the Media
  • For Subscribers

About

  • About the Journal
  • Editorial Board
  • Privacy Notice
  • Contact
  • Accessibility
(JNeurosci logo)
(SfN logo)

Copyright © 2025 by the Society for Neuroscience.
JNeurosci Online ISSN: 1529-2401

The ideas and opinions expressed in JNeurosci do not necessarily reflect those of SfN or the JNeurosci Editorial Board. Publication of an advertisement or other product mention in JNeurosci should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in JNeurosci.