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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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