Local low‐intensity vibration improves healing of muscle injury in mice

Abstract Recovery from traumatic muscle injuries is typically prolonged and incomplete. Our previous study demonstrated that whole‐body low‐intensity vibration (LIV) enhances healing in a mouse laceration model. We sought to determine whether locally applied LIV (a) improves muscle repair following...

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Main Authors: Thomas F. Corbiere, Timothy J. Koh
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.14356
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spelling doaj-db379120411e47ec91cf2c02c8b59c222020-11-25T03:25:17ZengWileyPhysiological Reports2051-817X2020-01-0182n/an/a10.14814/phy2.14356Local low‐intensity vibration improves healing of muscle injury in miceThomas F. Corbiere0Timothy J. Koh1Department of Kinesiology and Nutrition University of Illinois at Chicago Chicago IL USADepartment of Kinesiology and Nutrition University of Illinois at Chicago Chicago IL USAAbstract Recovery from traumatic muscle injuries is typically prolonged and incomplete. Our previous study demonstrated that whole‐body low‐intensity vibration (LIV) enhances healing in a mouse laceration model. We sought to determine whether locally applied LIV (a) improves muscle repair following injury in mice and (b) is directly transduced by cultured muscle cells, via increased IGF‐1 activity. C57BL/6J mice were subjected to laceration of the gastrocnemius muscle and were treated with LIV applied directly to the lower leg for 30 min/day or non‐LIV sham treatment (controls) for 7 or 14 days. LIV was also applied to differentiating myotubes in culture for 30 min/day for 3 or 6 days. Compared with control mice, LIV increased myofiber cross‐sectional area, diameter, and percent area of peripherally nucleated fibers, and decreased percent damaged area after 14 days of treatment. In cultured myotubes, LIV increased fusion and diameter compared with controls after 6 days of treatment. These LIV‐induced effects were associated with increased total Akt on day 7 in injured muscle and on day 3 in myotubes, whereas phosphorylated‐to‐total Akt ratio increased on day 14 in injured muscle and on day 6 in myotubes but were not associated with increased IGF‐1 levels at any time point. These changes were also associated with LIV‐induced suppression of FOXO1 and Atrogin‐1 gene expression at day 7 in injured muscle. These findings demonstrate that muscle cells can directly transduce LIV signals into increased growth and differentiation, and this effect is associated with increased Akt signaling.https://doi.org/10.14814/phy2.14356cell culturemechanical stimulationmouse modelmuscle repairskeletal muscle injury
collection DOAJ
language English
format Article
sources DOAJ
author Thomas F. Corbiere
Timothy J. Koh
spellingShingle Thomas F. Corbiere
Timothy J. Koh
Local low‐intensity vibration improves healing of muscle injury in mice
Physiological Reports
cell culture
mechanical stimulation
mouse model
muscle repair
skeletal muscle injury
author_facet Thomas F. Corbiere
Timothy J. Koh
author_sort Thomas F. Corbiere
title Local low‐intensity vibration improves healing of muscle injury in mice
title_short Local low‐intensity vibration improves healing of muscle injury in mice
title_full Local low‐intensity vibration improves healing of muscle injury in mice
title_fullStr Local low‐intensity vibration improves healing of muscle injury in mice
title_full_unstemmed Local low‐intensity vibration improves healing of muscle injury in mice
title_sort local low‐intensity vibration improves healing of muscle injury in mice
publisher Wiley
series Physiological Reports
issn 2051-817X
publishDate 2020-01-01
description Abstract Recovery from traumatic muscle injuries is typically prolonged and incomplete. Our previous study demonstrated that whole‐body low‐intensity vibration (LIV) enhances healing in a mouse laceration model. We sought to determine whether locally applied LIV (a) improves muscle repair following injury in mice and (b) is directly transduced by cultured muscle cells, via increased IGF‐1 activity. C57BL/6J mice were subjected to laceration of the gastrocnemius muscle and were treated with LIV applied directly to the lower leg for 30 min/day or non‐LIV sham treatment (controls) for 7 or 14 days. LIV was also applied to differentiating myotubes in culture for 30 min/day for 3 or 6 days. Compared with control mice, LIV increased myofiber cross‐sectional area, diameter, and percent area of peripherally nucleated fibers, and decreased percent damaged area after 14 days of treatment. In cultured myotubes, LIV increased fusion and diameter compared with controls after 6 days of treatment. These LIV‐induced effects were associated with increased total Akt on day 7 in injured muscle and on day 3 in myotubes, whereas phosphorylated‐to‐total Akt ratio increased on day 14 in injured muscle and on day 6 in myotubes but were not associated with increased IGF‐1 levels at any time point. These changes were also associated with LIV‐induced suppression of FOXO1 and Atrogin‐1 gene expression at day 7 in injured muscle. These findings demonstrate that muscle cells can directly transduce LIV signals into increased growth and differentiation, and this effect is associated with increased Akt signaling.
topic cell culture
mechanical stimulation
mouse model
muscle repair
skeletal muscle injury
url https://doi.org/10.14814/phy2.14356
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