Cargando…
Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling
It was observed that gravitational unloading during space missions and simulated microgravity in ground-based studies leads to both transformation of slow-twitch muscle fibers into fast-twitch fibers and to the elimination of support afferentation, leading to the “switching-off” of postural muscle m...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866401/ https://www.ncbi.nlm.nih.gov/pubmed/33573052 http://dx.doi.org/10.3390/ijms22031372 |
_version_ | 1783648067700916224 |
---|---|
author | Sharlo, Kristina A. Paramonova, Inna I. Lvova, Irina D. Mochalova, Ekaterina P. Kalashnikov, Vitaliy E. Vilchinskaya, Natalia A. Tyganov, Sergey A. Konstantinova, Tatyana S. Shevchenko, Tatiana F. Kalamkarov, Grigoriy R. Shenkman, Boris S. |
author_facet | Sharlo, Kristina A. Paramonova, Inna I. Lvova, Irina D. Mochalova, Ekaterina P. Kalashnikov, Vitaliy E. Vilchinskaya, Natalia A. Tyganov, Sergey A. Konstantinova, Tatyana S. Shevchenko, Tatiana F. Kalamkarov, Grigoriy R. Shenkman, Boris S. |
author_sort | Sharlo, Kristina A. |
collection | PubMed |
description | It was observed that gravitational unloading during space missions and simulated microgravity in ground-based studies leads to both transformation of slow-twitch muscle fibers into fast-twitch fibers and to the elimination of support afferentation, leading to the “switching-off” of postural muscle motor units electrical activity. In recent years, plantar mechanical stimulation (PMS) has been found to maintain the neuromuscular activity of the hindlimb muscles. Nitric oxide (NO) was shown to be one of the mediators of muscle fiber activity, which can also promote slow-type myosin expression. We hypothesized that applying PMS during rat hindlimb unloading would lead to NO production upregulation and prevention of the unloading-induced slow-to-fast fiber-type shift in rat soleus muscles. To test this hypothesis, Wistar rats were hindlimb suspended and subjected to daily PMS, and one group of PMS-subjected animals was also treated with nitric oxide synthase inhibitor (L-NAME). We discovered that PMS led to sustained NO level in soleus muscles of the suspended animals, and NOS inhibitor administration blocked this effect, as well as the positive effects of PMS on myosin I and IIa mRNA transcription and slow-to-fast fiber-type ratio during rat hindlimb unloading. The results of the study indicate that NOS activity is necessary for the PMS-mediated prevention of slow-to-fast fiber-type shift and myosin I and IIa mRNA transcription decreases during rat hindlimb unloading. |
format | Online Article Text |
id | pubmed-7866401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78664012021-02-07 Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling Sharlo, Kristina A. Paramonova, Inna I. Lvova, Irina D. Mochalova, Ekaterina P. Kalashnikov, Vitaliy E. Vilchinskaya, Natalia A. Tyganov, Sergey A. Konstantinova, Tatyana S. Shevchenko, Tatiana F. Kalamkarov, Grigoriy R. Shenkman, Boris S. Int J Mol Sci Article It was observed that gravitational unloading during space missions and simulated microgravity in ground-based studies leads to both transformation of slow-twitch muscle fibers into fast-twitch fibers and to the elimination of support afferentation, leading to the “switching-off” of postural muscle motor units electrical activity. In recent years, plantar mechanical stimulation (PMS) has been found to maintain the neuromuscular activity of the hindlimb muscles. Nitric oxide (NO) was shown to be one of the mediators of muscle fiber activity, which can also promote slow-type myosin expression. We hypothesized that applying PMS during rat hindlimb unloading would lead to NO production upregulation and prevention of the unloading-induced slow-to-fast fiber-type shift in rat soleus muscles. To test this hypothesis, Wistar rats were hindlimb suspended and subjected to daily PMS, and one group of PMS-subjected animals was also treated with nitric oxide synthase inhibitor (L-NAME). We discovered that PMS led to sustained NO level in soleus muscles of the suspended animals, and NOS inhibitor administration blocked this effect, as well as the positive effects of PMS on myosin I and IIa mRNA transcription and slow-to-fast fiber-type ratio during rat hindlimb unloading. The results of the study indicate that NOS activity is necessary for the PMS-mediated prevention of slow-to-fast fiber-type shift and myosin I and IIa mRNA transcription decreases during rat hindlimb unloading. MDPI 2021-01-29 /pmc/articles/PMC7866401/ /pubmed/33573052 http://dx.doi.org/10.3390/ijms22031372 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sharlo, Kristina A. Paramonova, Inna I. Lvova, Irina D. Mochalova, Ekaterina P. Kalashnikov, Vitaliy E. Vilchinskaya, Natalia A. Tyganov, Sergey A. Konstantinova, Tatyana S. Shevchenko, Tatiana F. Kalamkarov, Grigoriy R. Shenkman, Boris S. Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling |
title | Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling |
title_full | Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling |
title_fullStr | Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling |
title_full_unstemmed | Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling |
title_short | Plantar Mechanical Stimulation Maintains Slow Myosin Expression in Disused Rat Soleus Muscle via NO-Dependent Signaling |
title_sort | plantar mechanical stimulation maintains slow myosin expression in disused rat soleus muscle via no-dependent signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866401/ https://www.ncbi.nlm.nih.gov/pubmed/33573052 http://dx.doi.org/10.3390/ijms22031372 |
work_keys_str_mv | AT sharlokristinaa plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT paramonovainnai plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT lvovairinad plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT mochalovaekaterinap plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT kalashnikovvitaliye plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT vilchinskayanataliaa plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT tyganovsergeya plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT konstantinovatatyanas plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT shevchenkotatianaf plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT kalamkarovgrigoriyr plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling AT shenkmanboriss plantarmechanicalstimulationmaintainsslowmyosinexpressionindisusedratsoleusmusclevianodependentsignaling |