Chondroitin sulfate from Scophthalmus maximus for treating osteoarthritis

Int J Biol Macromol. 2018 Mar:108:1158-1164. doi: 10.1016/j.ijbiomac.2017.11.091. Epub 2017 Nov 14.

Abstract

Osteoarthritis (OA) is a common joint disease characterized by cartilage degradation. Chondroitin sulfate from shark (CS-S) has a good effect on OA in clinical, but due to source limited of CS from shark. Therefore, it is important to find a novel CS source with similar efficacy to CS-S in the treatment of OA. Herein, we reported a therapeutic effect of CS from scophthalmus maximus (CS-SM) for treating OA in rats. The OA model was established. After intervention with CS-SM by intragastric administration. Our results showed that CS-SM could protect articular cartilage in OA, inhibit the degradation of cartilage, decrease the apoptosis of chondrocytes, decline the content of interleukin-1, tumor necrosis factor-α and Prostaglandins E2 in synovial fluid, down-regulate the protein expression of matrix metalloproteinase-1 and up-regulate the protein expression of tissue inhibitor of metalloproteinase-1. Our results suggest that oral CS from SM is a new potential therapy for OA.

Keywords: Chondroitin sulfate; Osteoarthritis; Scophthalmus maximus.

MeSH terms

  • Animals
  • Cartilage, Articular / drug effects
  • Cartilage, Articular / pathology
  • Chondroitin Sulfates / pharmacology*
  • Chondroitin Sulfates / therapeutic use
  • Flatfishes*
  • Gene Expression Regulation / drug effects
  • Male
  • Matrix Metalloproteinase 1 / metabolism
  • Osteoarthritis / drug therapy*
  • Osteoarthritis / metabolism
  • Osteoarthritis / pathology
  • Rats
  • Synovial Fluid / drug effects
  • Synovial Fluid / metabolism
  • Tissue Inhibitor of Metalloproteinase-1 / metabolism

Substances

  • Tissue Inhibitor of Metalloproteinase-1
  • Chondroitin Sulfates
  • Matrix Metalloproteinase 1