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Single sarcomere contraction dynamics in a whole muscle
The instantaneous sarcomere length (SL) is regarded as an important indicator of the functional properties of striated muscle. Previously, we found greater sarcomere elongations at the distal end compared to the mid-portion in the mouse tibialis anterior (TA) when the muscle was stretched passively....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189036/ https://www.ncbi.nlm.nih.gov/pubmed/30323321 http://dx.doi.org/10.1038/s41598-018-33658-7 |
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author | Moo, Eng Kuan Herzog, Walter |
author_facet | Moo, Eng Kuan Herzog, Walter |
author_sort | Moo, Eng Kuan |
collection | PubMed |
description | The instantaneous sarcomere length (SL) is regarded as an important indicator of the functional properties of striated muscle. Previously, we found greater sarcomere elongations at the distal end compared to the mid-portion in the mouse tibialis anterior (TA) when the muscle was stretched passively. Here, we wanted to see if SL dispersions increase with activation, as has been observed in single myofibrils, and if SL dispersions differ for different locations in a muscle. Sarcomere lengths were measured at a mid- and a distal location of the TA in live mice using second harmonic generation imaging. Muscle force was measured using a tendon force transducer. We found that SL dispersions increased substantially from the passive to the active state, and were the same for the mid- and distal portions of TA. Sarcomere length non-uniformities within a segment of ~30 serial sarcomeres were up to 1.0 µm. We conclude from these findings that passive, mean SLs obtained from a single location are not necessarily representative of the distribution of SL in active muscle, and thus may be misinterpreted when deriving muscle mechanical properties, such as the force-length relationship. In view of these findings, it seems crucial to determine how SL distributions within a muscle relate to the most fundamental properties of muscle, such as the maximal isometric force. |
format | Online Article Text |
id | pubmed-6189036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61890362018-10-22 Single sarcomere contraction dynamics in a whole muscle Moo, Eng Kuan Herzog, Walter Sci Rep Article The instantaneous sarcomere length (SL) is regarded as an important indicator of the functional properties of striated muscle. Previously, we found greater sarcomere elongations at the distal end compared to the mid-portion in the mouse tibialis anterior (TA) when the muscle was stretched passively. Here, we wanted to see if SL dispersions increase with activation, as has been observed in single myofibrils, and if SL dispersions differ for different locations in a muscle. Sarcomere lengths were measured at a mid- and a distal location of the TA in live mice using second harmonic generation imaging. Muscle force was measured using a tendon force transducer. We found that SL dispersions increased substantially from the passive to the active state, and were the same for the mid- and distal portions of TA. Sarcomere length non-uniformities within a segment of ~30 serial sarcomeres were up to 1.0 µm. We conclude from these findings that passive, mean SLs obtained from a single location are not necessarily representative of the distribution of SL in active muscle, and thus may be misinterpreted when deriving muscle mechanical properties, such as the force-length relationship. In view of these findings, it seems crucial to determine how SL distributions within a muscle relate to the most fundamental properties of muscle, such as the maximal isometric force. Nature Publishing Group UK 2018-10-15 /pmc/articles/PMC6189036/ /pubmed/30323321 http://dx.doi.org/10.1038/s41598-018-33658-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Moo, Eng Kuan Herzog, Walter Single sarcomere contraction dynamics in a whole muscle |
title | Single sarcomere contraction dynamics in a whole muscle |
title_full | Single sarcomere contraction dynamics in a whole muscle |
title_fullStr | Single sarcomere contraction dynamics in a whole muscle |
title_full_unstemmed | Single sarcomere contraction dynamics in a whole muscle |
title_short | Single sarcomere contraction dynamics in a whole muscle |
title_sort | single sarcomere contraction dynamics in a whole muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189036/ https://www.ncbi.nlm.nih.gov/pubmed/30323321 http://dx.doi.org/10.1038/s41598-018-33658-7 |
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