4.3 Article

Diacerein reduces joint damage, pain behavior and inhibits transient receptor potential vanilloid 1, matrix metalloproteinase and glial cells in rat spinal cord

期刊

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
卷 20, 期 10, 页码 1337-1349

出版社

WILEY
DOI: 10.1111/1756-185X.12741

关键词

diacerein; glial cells; joint inflammation; MMP-9; pain; TRPV1

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel superior (CAPES)
  3. Fundacao de Amparo a Pesquisa e Inovacao do Estado de Santa Catarina (FAPESC), Brazil
  4. CAPES
  5. CNPq

向作者/读者索取更多资源

Aim: To investigate the antinociceptive, antiedematogenic and chondroprotective effects of diacerein (DIA) in a model of joint inflammation induced by complete Freund's adjuvant (CFA), as well as to investigate the involvement of metalloproteinase (MMP)-9, transient receptor potential vanilloid 1 (TRPV1) and glial cells in DIA's action mechanism. Methods: Complete Freund's adjuvant was injected into the knee joint of male rats. We observed mechanical and cold hypersensitivity, vocalization and spontaneous pain-related behaviors, as well as edema of the knee. Tissue samples of the knee were stained with Cason's technique and the thickness of the condilus cartilage was measured. Immunohistochemical analysis was performed on the spinal cord using anti-GFAP (glial fibrillary acidic protein), anti-MMP and anti-TRPV1 antibodies. Sections of the dorsal horns of the spinal cord were captured and an optical density was obtained. Results: Complete Freund's adjuvant induced mechanical and thermal hypersensitivity, as well as joint edema and changes in the synovial membrane and cartilage. DIA (30 mg/kg, orally, daily) significantly inhibited mechanical (58 +/- 10-87 +/- 3%) and thermal (66 +/- 12-87 +/- 8%) hypersensitivity, vocalization (83 +/- 541 +/- 11%), spontaneous pain score, joint swelling (60 +/- 6-40 +/- 9%), as well as the histological changes induced by CFA. In addition, DIA inhibited astrocyte activation, and prevented the increase of MMP-9 and TRPV1 expression in the spinal cord of the animals subjected to CFA injections. Conclusions: In short, this study shows that DIA reduces joint damage and hypersensitivity associated with inflammation induced by CFA through the inhibition of astroglial activation and decreases the expression of TRPV1 and MMP-9 in the rat spinal cord.

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