Low-level laser therapy (808 nm) contributes to muscle regeneration and prevents fibrosis in rat tibialis anterior muscle after cryolesion

Muscle regeneration is a complex phenomenon, involving replacement of damaged fibers by new muscle fibers. During this process, there is a tendency to form scar tissue or fibrosis by deposition of collagen that could be detrimental to muscle function. New therapies that could regulate fibrosis and f...

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Veröffentlicht in:Lasers in medical science 2013-05, Vol.28 (3), p.947-955
Hauptverfasser: Assis, Lívia, Moretti, Ana Iochabel Soares, Abrahão, Thalita Balsamo, de Souza, Heraldo Possolo, Hamblin, Michael R, Parizotto, Nivaldo Antonio
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container_issue 3
container_start_page 947
container_title Lasers in medical science
container_volume 28
creator Assis, Lívia
Moretti, Ana Iochabel Soares
Abrahão, Thalita Balsamo
de Souza, Heraldo Possolo
Hamblin, Michael R
Parizotto, Nivaldo Antonio
description Muscle regeneration is a complex phenomenon, involving replacement of damaged fibers by new muscle fibers. During this process, there is a tendency to form scar tissue or fibrosis by deposition of collagen that could be detrimental to muscle function. New therapies that could regulate fibrosis and favor muscle regeneration would be important for physical therapy. Low-level laser therapy (LLLT) has been studied for clinical treatment of skeletal muscle injuries and disorders, even though the molecular and cellular mechanisms have not yet been clarified. The aim of this study was to evaluate the effects of LLLT on molecular markers involved in muscle fibrosis and regeneration after cryolesion of the tibialis anterior (TA) muscle in rats. Sixty Wistar rats were randomly divided into three groups: control, injured TA muscle without LLLT, injured TA muscle treated with LLLT. The injured region was irradiated daily for four consecutive days, starting immediately after the lesion using an AlGaAs laser (808 nm, 30 mW, 180 J/cm 2 ; 3.8 W/cm 2 , 1.4 J). The animals were sacrificed on the fourth day after injury. LLLT significantly reduced the lesion percentage area in the injured muscle ( p  
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During this process, there is a tendency to form scar tissue or fibrosis by deposition of collagen that could be detrimental to muscle function. New therapies that could regulate fibrosis and favor muscle regeneration would be important for physical therapy. Low-level laser therapy (LLLT) has been studied for clinical treatment of skeletal muscle injuries and disorders, even though the molecular and cellular mechanisms have not yet been clarified. The aim of this study was to evaluate the effects of LLLT on molecular markers involved in muscle fibrosis and regeneration after cryolesion of the tibialis anterior (TA) muscle in rats. Sixty Wistar rats were randomly divided into three groups: control, injured TA muscle without LLLT, injured TA muscle treated with LLLT. The injured region was irradiated daily for four consecutive days, starting immediately after the lesion using an AlGaAs laser (808 nm, 30 mW, 180 J/cm 2 ; 3.8 W/cm 2 , 1.4 J). The animals were sacrificed on the fourth day after injury. LLLT significantly reduced the lesion percentage area in the injured muscle ( p  &lt; 0.05), increased mRNA levels of the transcription factors MyoD and myogenin ( p  &lt; 0.01) and the pro-angiogenic vascular endothelial growth factor ( p  &lt; 0.01). Moreover, LLLT decreased the expression of the profibrotic transforming growth factor TGF-β mRNA ( p  &lt; 0.01) and reduced type I collagen deposition ( p  &lt; 0.01). 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During this process, there is a tendency to form scar tissue or fibrosis by deposition of collagen that could be detrimental to muscle function. New therapies that could regulate fibrosis and favor muscle regeneration would be important for physical therapy. Low-level laser therapy (LLLT) has been studied for clinical treatment of skeletal muscle injuries and disorders, even though the molecular and cellular mechanisms have not yet been clarified. The aim of this study was to evaluate the effects of LLLT on molecular markers involved in muscle fibrosis and regeneration after cryolesion of the tibialis anterior (TA) muscle in rats. Sixty Wistar rats were randomly divided into three groups: control, injured TA muscle without LLLT, injured TA muscle treated with LLLT. The injured region was irradiated daily for four consecutive days, starting immediately after the lesion using an AlGaAs laser (808 nm, 30 mW, 180 J/cm 2 ; 3.8 W/cm 2 , 1.4 J). The animals were sacrificed on the fourth day after injury. LLLT significantly reduced the lesion percentage area in the injured muscle ( p  &lt; 0.05), increased mRNA levels of the transcription factors MyoD and myogenin ( p  &lt; 0.01) and the pro-angiogenic vascular endothelial growth factor ( p  &lt; 0.01). Moreover, LLLT decreased the expression of the profibrotic transforming growth factor TGF-β mRNA ( p  &lt; 0.01) and reduced type I collagen deposition ( p  &lt; 0.01). These results suggest that LLLT could be an effective therapeutic approach for promoting skeletal muscle regeneration while preventing tissue fibrosis after muscle injury.</abstract><cop>London</cop><pub>Springer-Verlag</pub><pmid>22898787</pmid><doi>10.1007/s10103-012-1183-3</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Collagen Type I - metabolism
Dentistry
Fibrosis
Injuries
Lasers
Lasers, Semiconductor - therapeutic use
Low-Level Light Therapy
Male
Medicine
Medicine & Public Health
Muscle, Skeletal - injuries
Muscle, Skeletal - metabolism
Muscle, Skeletal - radiation effects
Muscular system
MyoD Protein - genetics
Myogenin - genetics
Optical Devices
Optics
Original Article
Photonics
Quantum Optics
Rats
Rats, Wistar
Regeneration - genetics
Regeneration - physiology
Regeneration - radiation effects
RNA, Messenger - genetics
RNA, Messenger - metabolism
Rodents
Transforming Growth Factor beta1 - genetics
Vascular Endothelial Growth Factor A - genetics
title Low-level laser therapy (808 nm) contributes to muscle regeneration and prevents fibrosis in rat tibialis anterior muscle after cryolesion
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