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      Infrared Low-Level Laser Therapy (Photobiomodulation Therapy) before Intense Progressive Running Test of High-Level Soccer Players: Effects on Functional, Muscle Damage, Inflammatory, and Oxidative Stress Markers—A Randomized Controlled Trial

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          Abstract

          The effects of preexercise photobiomodulation therapy (PBMT) to enhance performance, accelerate recovery, and attenuate exercise-induced oxidative stress were still not fully investigated, especially in high-level athletes. The aim of this study was to evaluate the effects of PBMT (using infrared low-level laser therapy) applied before a progressive running test on functional aspects, muscle damage, and inflammatory and oxidative stress markers in high-level soccer players. A randomized, triple-blind, placebo-controlled crossover trial was performed. Twenty-two high-level male soccer players from the same team were recruited and treated with active PBMT and placebo. The order of interventions was randomized. Immediately after the application of active PBMT or placebo, the volunteers performed a standardized high-intensity progressive running test (ergospirometry test) until exhaustion. We analyzed rates of oxygen uptake (VO 2 max), time until exhaustion, and aerobic and anaerobic threshold during the intense progressive running test. Creatine kinase (CK) and lactate dehydrogenase (LDH) activities, levels of interleukin-1 β (IL-1- β), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF- α), levels of thiobarbituric acid (TBARS) and carbonylated proteins, and catalase (CAT) and superoxide dismutase (SOD) activities were measured before and five minutes after the end of the test. PBMT increased the VO 2 max (both relative and absolute values— p < 0.0467 and p < 0.0013, respectively), time until exhaustion ( p < 0.0043), time ( p < 0.0007) and volume ( p < 0.0355) in which anaerobic threshold happened, and volume in which aerobic threshold happened ( p < 0.0068). Moreover, PBMT decreased CK ( p < 0.0001) and LDH ( p < 0.0001) activities. Regarding the cytokines, PBMT decreased only IL-6 ( p < 0.0001). Finally, PBMT decreased TBARS ( p < 0.0001) and carbonylated protein levels ( p < 0.01) and increased SOD ( p < 0.0001)and CAT ( p < 0.0001) activities. The findings of this study demonstrate that preexercise PBMT acts on different functional aspects and biochemical markers. Moreover, preexercise PBMT seems to play an important antioxidant effect, decreasing exercise-induced oxidative stress and consequently enhancing athletic performance and improving postexercise recovery. This trial is registered with Clinicaltrials.gov NCT03803956.

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          Most cited references47

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          Determination of carbonyl content in oxidatively modified proteins.

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            The effects of physical activity on serum C-reactive protein and inflammatory markers: a systematic review.

            Physical activity is associated with a reduced incidence of coronary disease, but the mechanisms mediating this effect are not defined. There has been considerable recent interest in inflammation in the pathogenesis of cardiovascular disease. Some of the beneficial role of physical activity may result from its effects on the inflammatory process. We searched PubMed for articles published between 1975 through May 2004 using the terms exercise, physical activity, or physical fitness combined with C-reactive protein, inflammation, inflammatory markers, or cytokines. The review revealed 19 articles on the acute inflammatory response to exercise, 18 on cross-sectional comparisons of subjects by activity levels, and 5 examining prospectively the effects of exercise training on the inflammatory process. Exercise produces a short-term, inflammatory response, whereas both cross-sectional comparisons and longitudinal exercise training studies demonstrate a long-term "anti-inflammatory" effect. This anti-inflammatory response may contribute to the beneficial effects of habitual physical activity.
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              Biochemical markers of muscular damage.

              Muscle tissue may be damaged following intense prolonged training as a consequence of both metabolic and mechanical factors. Serum levels of skeletal muscle enzymes or proteins are markers of the functional status of muscle tissue, and vary widely in both pathological and physiological conditions. Creatine kinase, lactate dehydrogenase, aldolase, myoglobin, troponin, aspartate aminotransferase, and carbonic anhydrase CAIII are the most useful serum markers of muscle injury, but apoptosis in muscle tissues subsequent to strenuous exercise may be also triggered by increased oxidative stress. Therefore, total antioxidant status can be used to evaluate the level of stress in muscle by other markers, such as thiobarbituric acid-reactive substances, malondialdehyde, sulfhydril groups, reduced glutathione, oxidized glutathione, superoxide dismutase, catalase and others. As the various markers provide a composite picture of muscle status, we recommend using more than one to provide a better estimation of muscle stress.
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                Author and article information

                Contributors
                Journal
                Oxid Med Cell Longev
                Oxid Med Cell Longev
                OMCL
                Oxidative Medicine and Cellular Longevity
                Hindawi
                1942-0900
                1942-0994
                2019
                16 November 2019
                : 2019
                : 6239058
                Affiliations
                1Physiotherapy Research Group, Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway
                2Laboratory of Phototherapy and Innovative Technologies in Health (LaPIT), Nove de Julho University, São Paulo, SP, Brazil
                3Postgraduate Program in Rehabilitation Sciences, Nove de Julho University, São Paulo, SP, Brazil
                4Faculty Cenecista of Bento Gonçalves (CNEC), Bento Gonçalves, RS, Brazil
                Author notes

                Guest Editor: José R. Pinto

                Author information
                https://orcid.org/0000-0002-1669-9675
                https://orcid.org/0000-0001-9624-4103
                https://orcid.org/0000-0001-6393-7616
                Article
                10.1155/2019/6239058
                6885272
                31827687
                81f243e9-33d6-482b-9a4b-1d8d7ff67736
                Copyright © 2019 Shaiane Silva Tomazoni et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 20 February 2019
                : 9 October 2019
                Funding
                Funded by: National Council for Scientific and Technological Development
                Award ID: 310281/2017-2
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo
                Award ID: 2017/06422-5
                Award ID: 2010/52404-0
                Categories
                Clinical Study

                Molecular medicine
                Molecular medicine

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