Fursultiamine, a vitamin B1 derivative, enhances chondroprotective effects of glucosamine hydrochloride and chondroitin sulfate in rabbit experimental osteoarthritis

Inflamm Res. 2005 Jun;54(6):249-55. doi: 10.1007/s00011-005-1351-z.

Abstract

Object and design: The therapeutic effect of glucosamine hydrochloride (GH) and chondroitin sulfate (CS) in combination with fursultiamine, a vitamin B1 derivative, on the development of cartilage lesions was investigated in an animal model of osteoarthritis (OA).

Methods: The OA model was created by partial medial meniscectomy of the right knee joint (day 0). The rabbits were placed into three experimental groups: operated (OA) rabbits that received placebo treatment, OA rabbits that received GH (1000 mg/kg) + CS (800 mg/kg), and OA rabbits that received GH + CS + fursultiamine (100 mg/kg). Each treatment was initiated on day 3 and continued for 8 weeks. Macroscopic and histologic analyses were performed on the cartilage. The level of MMP-1 in OA cartilage chondrocytes was evaluated by immunohistochemistry.

Results: Only the group receiving combined treatment with GH + CS + fursultiamine showed a significant reduction in the severity of macroscopic and histologic lesions on tibial plateau, which is the weight bearing cartilage surface of the tibia, compared with placebo-treated OA rabbits. This treatment group also revealed a small, but significant, decrease in the body weight gain of the rabbits. In cartilage from placebo-treated OA rabbits, a significantly higher percentage of chondrocytes in superficial layer stained positive for MMP-1 compared with unoperated control. Rabbits treated with the GH + CS + fursultiamine revealed a significant reduction in the level of MMP-1.

Conclusion: These results suggest that the chondroprotective effect of GH + CS is enhanced by the addition of fursultiamine in experimental OA. This effect was associated with a reduction in the level of MMP-1, which are known to play an important role in the pathophysiology of OA lesions.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Cartilage / metabolism
  • Cartilage / pathology
  • Chondroitin Sulfates / therapeutic use*
  • Disease Models, Animal*
  • Disease Progression
  • Fursultiamin / chemistry
  • Fursultiamin / pharmacology*
  • Fursultiamin / therapeutic use
  • Glucosamine / therapeutic use*
  • Immunohistochemistry
  • Male
  • Matrix Metalloproteinase 1 / metabolism
  • Osteoarthritis / drug therapy*
  • Osteoarthritis / pathology
  • Protective Agents / chemistry
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use
  • Rabbits
  • Tibia / metabolism
  • Tibia / pathology

Substances

  • Protective Agents
  • Fursultiamin
  • Chondroitin Sulfates
  • Matrix Metalloproteinase 1
  • Glucosamine