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The control and training of single motor units in isometric tasks are constrained by a common input signal
Recent developments in neural interfaces enable the real-time and non-invasive tracking of motor neuron spiking activity. Such novel interfaces could provide a promising basis for human motor augmentation by extracting potentially high-dimensional control signals directly from the human nervous syst...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208758/ https://www.ncbi.nlm.nih.gov/pubmed/35670561 http://dx.doi.org/10.7554/eLife.72871 |
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author | Bräcklein, Mario Barsakcioglu, Deren Yusuf Ibáñez, Jaime Eden, Jonathan Burdet, Etienne Mehring, Carsten Farina, Dario |
author_facet | Bräcklein, Mario Barsakcioglu, Deren Yusuf Ibáñez, Jaime Eden, Jonathan Burdet, Etienne Mehring, Carsten Farina, Dario |
author_sort | Bräcklein, Mario |
collection | PubMed |
description | Recent developments in neural interfaces enable the real-time and non-invasive tracking of motor neuron spiking activity. Such novel interfaces could provide a promising basis for human motor augmentation by extracting potentially high-dimensional control signals directly from the human nervous system. However, it is unclear how flexibly humans can control the activity of individual motor neurons to effectively increase the number of degrees of freedom available to coordinate multiple effectors simultaneously. Here, we provided human subjects (N = 7) with real-time feedback on the discharge patterns of pairs of motor units (MUs) innervating a single muscle (tibialis anterior) and encouraged them to independently control the MUs by tracking targets in a 2D space. Subjects learned control strategies to achieve the target-tracking task for various combinations of MUs. These strategies rarely corresponded to a volitional control of independent input signals to individual MUs during the onset of neural activity. Conversely, MU activation was consistent with a common input to the MU pair, while individual activation of the MUs in the pair was predominantly achieved by alterations in de-recruitment order that could be explained by history-dependent changes in motor neuron excitability. These results suggest that flexible MU recruitment based on independent synaptic inputs to single MUs is unlikely, although de-recruitment might reflect varying inputs or modulations in the neuron’s intrinsic excitability. |
format | Online Article Text |
id | pubmed-9208758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92087582022-06-21 The control and training of single motor units in isometric tasks are constrained by a common input signal Bräcklein, Mario Barsakcioglu, Deren Yusuf Ibáñez, Jaime Eden, Jonathan Burdet, Etienne Mehring, Carsten Farina, Dario eLife Neuroscience Recent developments in neural interfaces enable the real-time and non-invasive tracking of motor neuron spiking activity. Such novel interfaces could provide a promising basis for human motor augmentation by extracting potentially high-dimensional control signals directly from the human nervous system. However, it is unclear how flexibly humans can control the activity of individual motor neurons to effectively increase the number of degrees of freedom available to coordinate multiple effectors simultaneously. Here, we provided human subjects (N = 7) with real-time feedback on the discharge patterns of pairs of motor units (MUs) innervating a single muscle (tibialis anterior) and encouraged them to independently control the MUs by tracking targets in a 2D space. Subjects learned control strategies to achieve the target-tracking task for various combinations of MUs. These strategies rarely corresponded to a volitional control of independent input signals to individual MUs during the onset of neural activity. Conversely, MU activation was consistent with a common input to the MU pair, while individual activation of the MUs in the pair was predominantly achieved by alterations in de-recruitment order that could be explained by history-dependent changes in motor neuron excitability. These results suggest that flexible MU recruitment based on independent synaptic inputs to single MUs is unlikely, although de-recruitment might reflect varying inputs or modulations in the neuron’s intrinsic excitability. eLife Sciences Publications, Ltd 2022-06-07 /pmc/articles/PMC9208758/ /pubmed/35670561 http://dx.doi.org/10.7554/eLife.72871 Text en © 2022, Bräcklein 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 Bräcklein, Mario Barsakcioglu, Deren Yusuf Ibáñez, Jaime Eden, Jonathan Burdet, Etienne Mehring, Carsten Farina, Dario The control and training of single motor units in isometric tasks are constrained by a common input signal |
title | The control and training of single motor units in isometric tasks are constrained by a common input signal |
title_full | The control and training of single motor units in isometric tasks are constrained by a common input signal |
title_fullStr | The control and training of single motor units in isometric tasks are constrained by a common input signal |
title_full_unstemmed | The control and training of single motor units in isometric tasks are constrained by a common input signal |
title_short | The control and training of single motor units in isometric tasks are constrained by a common input signal |
title_sort | control and training of single motor units in isometric tasks are constrained by a common input signal |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208758/ https://www.ncbi.nlm.nih.gov/pubmed/35670561 http://dx.doi.org/10.7554/eLife.72871 |
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