Login / Signup

Photobiomodulation effects in metalloproteinases expression in zymosan-induced arthritis.

Lucia Mara Januário Dos AnjosAnna Cecília Quirino-TeixeiraEugenio Damasceno HottzAdenilson de Souza da FonsecaJacy GameiroFlávia de Paoli
Published in: Lasers in medical science (2022)
Matrix metalloproteinases (MMPs) play a crucial role in the degenerative course of rheumatic disorders. They are responsible for cartilage and other joint-associated tissues breakdown. Amid arthritis treatments, photobiostimulation (PBM), a non-thermal and non-invasive low-power laser application, appears to be an outstanding therapy alternative once it has succeeded in MMPs modulation. Thus, this study aimed to evaluate the PBM effects of low infrared laser (830 nm), testing two different energy densities (3 and 30 Jcm -2 ) in MMP-2, MMP-9, MMP-13, and MMP-14 as well as the inhibitor TIMP-2 expressions using zymosan-induced arthritis model. C57BL/6 mice were distributed into four groups (n = 8): zymosan-induced arthritis without treatment; zymosan-induced arthritis and dexamethasone-treated; zymosan-induced arthritis and PBM at energy density of 3 Jcm -2 treated; and zymosan-induced arthritis and PBM at energy density of 30 Jcm -2 treated. MMPs and TIMP-2 mRNA relative levels by qRT-PCR and proteins expression by immunohistochemical and Western blotting techniques were performed after PBM treatment in the inflamed joint. Our results demonstrated PBM could modulate both mRNA relative levels and proteins expression of the MMP-2, -9, -13, -14, and TIMP-2 in joint tissues, decreasing MMP-9 protein expression and increasing TIMP-2 protein expression. PBM promotes a better arthritis prognostic, modulating metalloproteinase and its inhibitor, especially MMP-9 and TIMP-2 protein expression that is important inflammatory markers. These findings may also corroborate that PBM may regulate MMPs expression using different pathways.
Keyphrases
  • rheumatoid arthritis
  • high glucose
  • diabetic rats
  • poor prognosis
  • cell migration
  • gene expression
  • endothelial cells
  • binding protein
  • stem cells
  • bone marrow
  • metabolic syndrome
  • skeletal muscle
  • newly diagnosed