Lívia Assis, Ana Cláudia Muniz Rennó, C. Bublitz, Aya Hirai, Gabriela Harada, H. Kido, Fernanda de Freitas Anibal, L. Yamauchi
{"title":"Laser therapy modulates systemic inflammatory processes and muscle atrophy in an experimental model of sepsis in rats","authors":"Lívia Assis, Ana Cláudia Muniz Rennó, C. Bublitz, Aya Hirai, Gabriela Harada, H. Kido, Fernanda de Freitas Anibal, L. Yamauchi","doi":"10.1515/plm-2015-0007","DOIUrl":null,"url":null,"abstract":"Abstract Objective: The aim of this study was to determine the effectiveness of low-level laser therapy (LLLT) on the modulation of the systemic inflammatory processes and skeletal muscle morphology in an experimental sepsis model (cecal ligation and puncture, CLP). Study design: Seventy-two male Wistar rats were randomly divided into three groups: control group (CG); sepsis group (SG) where rats were submitted to CLP but without LLLT treatment, and the sepsis laser-treated group (SLG). Laser irradiation (GaAlAs laser, continuous wave, 808 nm, 30 mW, 48 s, 30 J/cm2, 0.028 cm2, 1.07 mW/cm2) was performed immediately after surgery and every 24 h at 4 points (on the middle of tibialis anterior and diaphragm, bilaterally), through the punctual contact technique. All sepsis animals were sacrificed at 6, 24, 48 and 72 h post-surgery. The immunohistochemistry analysis was used to verify the expression of proteins related to the regulation of muscle wasting (MuRF-1 and atrogin). In order to investigate the action of LLLT on inflammatory mediators in the rat sepsis model, two inflammatory cytokines IL-6 and IL-10, were evaluated. Results: The results showed that the laser-treated animals presented a lower IL-6 activity and decreased atrogin and MuRF-1 immunoexpression. However, no difference was observed in muscle cross-sectional area between the experimental groups. Conclusion: These results suggest that LLLT was able to decrease the systemic inflammation and muscle atrophy markers, preventing muscle protein degradation.","PeriodicalId":20126,"journal":{"name":"Photonics & Lasers in Medicine","volume":"51 1","pages":"241 - 251"},"PeriodicalIF":0.0000,"publicationDate":"2015-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Photonics & Lasers in Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/plm-2015-0007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Abstract Objective: The aim of this study was to determine the effectiveness of low-level laser therapy (LLLT) on the modulation of the systemic inflammatory processes and skeletal muscle morphology in an experimental sepsis model (cecal ligation and puncture, CLP). Study design: Seventy-two male Wistar rats were randomly divided into three groups: control group (CG); sepsis group (SG) where rats were submitted to CLP but without LLLT treatment, and the sepsis laser-treated group (SLG). Laser irradiation (GaAlAs laser, continuous wave, 808 nm, 30 mW, 48 s, 30 J/cm2, 0.028 cm2, 1.07 mW/cm2) was performed immediately after surgery and every 24 h at 4 points (on the middle of tibialis anterior and diaphragm, bilaterally), through the punctual contact technique. All sepsis animals were sacrificed at 6, 24, 48 and 72 h post-surgery. The immunohistochemistry analysis was used to verify the expression of proteins related to the regulation of muscle wasting (MuRF-1 and atrogin). In order to investigate the action of LLLT on inflammatory mediators in the rat sepsis model, two inflammatory cytokines IL-6 and IL-10, were evaluated. Results: The results showed that the laser-treated animals presented a lower IL-6 activity and decreased atrogin and MuRF-1 immunoexpression. However, no difference was observed in muscle cross-sectional area between the experimental groups. Conclusion: These results suggest that LLLT was able to decrease the systemic inflammation and muscle atrophy markers, preventing muscle protein degradation.