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  • Effects of photobiomodulati...
    Silva, Tamiris; Fragoso, Yara Dadalti; Destro Rodrigues, Maria Fernanda Setúbal; Gomes, Andréa Oliver; da Silva, Fernanda Cordeiro; Andreo, Lucas; Viana, Ariane; Teixeira da Silva, Daniela de Fátima; Chavantes, Maria Cristina; Tempestini Horliana, Anna Carolina Ratto; De Angelis, Kátia; Deana, Alessandro Melo; Branco, Luciana Prats; Santos Fernandes, Kristianne Porta; Motta, Lara Jansiski; Mesquita-Ferrari, Raquel Agnelli; Bussadori, Sandra Kalil

    PloS one, 04/2020, Volume: 15, Issue: 4
    Journal Article

    Investigate the effects of photobiomodulation (PBM) on the expression of IL-10 and nitrites in individuals with Relapsing-Remitting multiple sclerosis (MS), as these biomarkers play a fundamental role in the physiopathology of the disease. The modulation of IL-10 and nitrites through treatment with PBM may be a novel treatment modality for MS. A randomized, uncontrolled, clinical trial was conducted involving 14 individuals with a diagnosis of Relapsing-Remitting MS and a score of up to 6.0 on the Expanded Disability Status Scale (EDSS). Group 1 -PBM in the sublingual region; Group 2 -PBM over the radial artery. Irradiation was administered with a wavelength of 808 nm and output power of 100 mW for 360 seconds twice a week, totaling 24 sessions. Peripheral blood was analyzed for the determination of serum levels of IL-10 and nitrites. After treatment with PBM, the expression of IL-10 increased in both the sublingual group (pre-treatment: 2.8 ± 1.4 pg/ml; post-treatment: 8.3 ± 2.4 pg/ml) and the radial artery group (pre-treatment: 2.7 pg/ml ± 1.4; post-treatment: 11.7 ± 3.8 pg/ml). In contrast, nitrite levels were not modulated in the sublingual group (pre-treatment: 65 ± 50 nmol/mg protein; post-treatment: 51 ± 42 nmol/mg protein) or the radial artery group (pre-treatment: 51 ± 16 nmol/mg protein; post-treatment: 42 ± 7 nmol/mg protein). Treatment with PBM positively modulated the expression of IL-10 but had no effect on nitrite levels. Further studies should be conducted with a larger sample and a control group, as PBM may be a promising complementary treatment for the management of MS. This trial is registered at ClinicalTrials.gov. Identifier: NCT03360487.