Anti-Inflammatory Effect of Ebosin on Rat Collagen-Induced Arthritis through Suppressing Production of Interleukin-1β, Interleukin-6 and Tumor Necrosis Factor-α

Author:

Zhang Y.1,Wang L.F.1,Bai J.Y.2,Guan M.Z.2,Jiang R.1,Guo L.H.1,Wu J.B.1,Zhang R.3,Cheng G.F.2,Li Y.1

Affiliation:

1. Key Laboratory of Biotechnology of Antibiotics, Ministry of Health, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

2. Institute of Material Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

3. School of Biological Sciences, University of Wollongong, NSW, Australia

Abstract

Reumatoid arthritis (RA) is an autoimmune disease which has been studied experimentally using a wide variety of animal models including collagen-induced arthritis (CIA). Using this CIA model we studied the therapeutic effects and mechanism of action of Ebosin, a novel exopolysaccharide produced by Streptomyces sp. 139, on arthritis. Ebosin at 200, 400 and 600 mg/kg/day was orally administered to rats respectively between day 10 and 30 after immunization with chicken type II collagen. With the treatment arthritic progression was remarkably suppressed. Levels of anti-type II collagen-specific antibody, IL-1β and TNF-α were significantly lower in the Ebosin-treated CIA rats compared with the untreated controls. In cultured fibroblast-like synoviocytes (FLS), remarkable suppression of IL-1β, TNF-α and IL-6 production was detected at both protein and mRNA levels after Ebosin administration. Ebosin also resulted in lower activities of IL-1β-converting enzyme and TNF-α-converting enzyme in FLS. Based on these results, it is concluded that development and progression of rat CIA can be significantly suppressed by orally-administrated Ebosin. The therapeutic effect may be attributed to its inhibition in the production of IL-1β, TNF-α and IL-6 in the CIA rats.

Publisher

SAGE Publications

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