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Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats

Following active muscle shortening, steady‐state isometric force is less than a purely isometric contraction at the same muscle length and level of activation; this is known as residual force depression (rFD). It is unknown whether rFD at the single muscle fiber level can be modified via training. H...

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Autores principales: Mashouri, Parastoo, Chen, Jackey, Noonan, Alex M., Brown, Stephen H. M., Power, Geoffrey A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839327/
https://www.ncbi.nlm.nih.gov/pubmed/33502825
http://dx.doi.org/10.14814/phy2.14725
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author Mashouri, Parastoo
Chen, Jackey
Noonan, Alex M.
Brown, Stephen H. M.
Power, Geoffrey A.
author_facet Mashouri, Parastoo
Chen, Jackey
Noonan, Alex M.
Brown, Stephen H. M.
Power, Geoffrey A.
author_sort Mashouri, Parastoo
collection PubMed
description Following active muscle shortening, steady‐state isometric force is less than a purely isometric contraction at the same muscle length and level of activation; this is known as residual force depression (rFD). It is unknown whether rFD at the single muscle fiber level can be modified via training. Here we investigated whether rFD in single muscle fibers is modifiable through downhill and uphill running in the extensor digitorum longus (EDL) and soleus (SOL) muscles in rats. Rats were run uphill or downhill 5 days/week for 4 weeks. After muscles were dissected and chemically permeabilized, single fibers were tied between a length controller and force transducer, transferred to an activating solution, with ATP and pCa of 4.2 for mechanical testing. rFD was quantified after active fiber shortening from an average sarcomere length (SL) of 3.1–2.5 µm at a relative speed of 0.15 fiber lengths/s (slow) and 0.6 fiber lengths/s (fast). rFD was calculated as the difference in force (normalized to cross‐sectional area) during the isometric steady‐state phase following active shortening and the purely isometric contraction. In addition to rFD, mechanical work of shortening and stiffness depression were also calculated. rFD was present for both the EDL (6–15%) and SOL (1–2%) muscles, with no effect of training. rFD was greater for the EDL than SOL which closely corresponded to the greater stiffness depression in the EDL, indicating a greater inhibition of cross‐bridge attachments. These results indicate that while rFD was observed, training did not appear to alter this intrinsic history‐dependent property of single muscle fibers.
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spelling pubmed-78393272021-02-04 Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats Mashouri, Parastoo Chen, Jackey Noonan, Alex M. Brown, Stephen H. M. Power, Geoffrey A. Physiol Rep Original Research Following active muscle shortening, steady‐state isometric force is less than a purely isometric contraction at the same muscle length and level of activation; this is known as residual force depression (rFD). It is unknown whether rFD at the single muscle fiber level can be modified via training. Here we investigated whether rFD in single muscle fibers is modifiable through downhill and uphill running in the extensor digitorum longus (EDL) and soleus (SOL) muscles in rats. Rats were run uphill or downhill 5 days/week for 4 weeks. After muscles were dissected and chemically permeabilized, single fibers were tied between a length controller and force transducer, transferred to an activating solution, with ATP and pCa of 4.2 for mechanical testing. rFD was quantified after active fiber shortening from an average sarcomere length (SL) of 3.1–2.5 µm at a relative speed of 0.15 fiber lengths/s (slow) and 0.6 fiber lengths/s (fast). rFD was calculated as the difference in force (normalized to cross‐sectional area) during the isometric steady‐state phase following active shortening and the purely isometric contraction. In addition to rFD, mechanical work of shortening and stiffness depression were also calculated. rFD was present for both the EDL (6–15%) and SOL (1–2%) muscles, with no effect of training. rFD was greater for the EDL than SOL which closely corresponded to the greater stiffness depression in the EDL, indicating a greater inhibition of cross‐bridge attachments. These results indicate that while rFD was observed, training did not appear to alter this intrinsic history‐dependent property of single muscle fibers. John Wiley and Sons Inc. 2021-01-27 /pmc/articles/PMC7839327/ /pubmed/33502825 http://dx.doi.org/10.14814/phy2.14725 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Mashouri, Parastoo
Chen, Jackey
Noonan, Alex M.
Brown, Stephen H. M.
Power, Geoffrey A.
Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
title Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
title_full Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
title_fullStr Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
title_full_unstemmed Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
title_short Modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
title_sort modifiability of residual force depression in single muscle fibers following uphill and downhill training in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839327/
https://www.ncbi.nlm.nih.gov/pubmed/33502825
http://dx.doi.org/10.14814/phy2.14725
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