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Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement
People and animals can move freely, but they must also be able to stay still. How do skeletal muscles economically produce both movement and posture? Humans are well known to have motor units with relatively homogeneous mechanical properties. Thixotropic muscle properties can provide a solution by p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892447/ https://www.ncbi.nlm.nih.gov/pubmed/27293785 http://dx.doi.org/10.1098/rsos.160065 |
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author | Vernooij, Carlijn A. Reynolds, Raymond F. Lakie, Martin |
author_facet | Vernooij, Carlijn A. Reynolds, Raymond F. Lakie, Martin |
author_sort | Vernooij, Carlijn A. |
collection | PubMed |
description | People and animals can move freely, but they must also be able to stay still. How do skeletal muscles economically produce both movement and posture? Humans are well known to have motor units with relatively homogeneous mechanical properties. Thixotropic muscle properties can provide a solution by providing a temporary stiffening of all skeletal muscles in postural conditions. This stiffening is alleviated almost instantly when muscles start to move. In this paper, we probe this behaviour. We monitor both the neural input to a muscle, measured here as extensor muscle electromyography (EMG), and its output, measured as tremor (finger acceleration). Both signals were analysed continuously as the subject made smooth transitions between posture and movement. The results showed that there were marked changes in tremor which systematically increased in size and decreased in frequency as the subject moved faster. By contrast, the EMG changed little and reflected muscle force requirement rather than movement speed. The altered tremor reflects naturally occurring thixotropic changes in muscle behaviour. Our results suggest that physiological tremor provides useful and hitherto unrecognized insights into skeletal muscle's role in posture and movement. |
format | Online Article Text |
id | pubmed-4892447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48924472016-06-10 Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement Vernooij, Carlijn A. Reynolds, Raymond F. Lakie, Martin R Soc Open Sci Biology (Whole Organism) People and animals can move freely, but they must also be able to stay still. How do skeletal muscles economically produce both movement and posture? Humans are well known to have motor units with relatively homogeneous mechanical properties. Thixotropic muscle properties can provide a solution by providing a temporary stiffening of all skeletal muscles in postural conditions. This stiffening is alleviated almost instantly when muscles start to move. In this paper, we probe this behaviour. We monitor both the neural input to a muscle, measured here as extensor muscle electromyography (EMG), and its output, measured as tremor (finger acceleration). Both signals were analysed continuously as the subject made smooth transitions between posture and movement. The results showed that there were marked changes in tremor which systematically increased in size and decreased in frequency as the subject moved faster. By contrast, the EMG changed little and reflected muscle force requirement rather than movement speed. The altered tremor reflects naturally occurring thixotropic changes in muscle behaviour. Our results suggest that physiological tremor provides useful and hitherto unrecognized insights into skeletal muscle's role in posture and movement. The Royal Society 2016-05-04 /pmc/articles/PMC4892447/ /pubmed/27293785 http://dx.doi.org/10.1098/rsos.160065 Text en http://creativecommons.org/licenses/by/4.0/ © 2016 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biology (Whole Organism) Vernooij, Carlijn A. Reynolds, Raymond F. Lakie, Martin Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
title | Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
title_full | Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
title_fullStr | Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
title_full_unstemmed | Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
title_short | Physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
title_sort | physiological tremor reveals how thixotropy adapts skeletal muscle for posture and movement |
topic | Biology (Whole Organism) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892447/ https://www.ncbi.nlm.nih.gov/pubmed/27293785 http://dx.doi.org/10.1098/rsos.160065 |
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