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Methyl salicylate lactoside inhibits inflammatory response of fibroblast‐like synoviocytes and joint destruction in collagen‐induced arthritis in mice
Author(s) -
Xin Wenyu,
Huang Chao,
Zhang Xue,
Xin Sheng,
Zhou Yiming,
Ma Xiaowei,
Zhang Dan,
Li Yongjie,
Zhou Sibai,
Zhang Dongming,
Zhang Tiantai,
Du Guanhua
Publication year - 2014
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.12715
Subject(s) - arthritis , in vivo , pharmacology , rheumatoid arthritis , cancer research , osteoarthritis , cytokine , tumor necrosis factor alpha , medicine , chemistry , immunology , pathology , biology , alternative medicine , microbiology and biotechnology
Background and Purpose Methyl salicylate 2‐ O ‐β‐ d ‐lactoside ( MSL ), whose chemical structure is similar to that of salicylic acid, is a natural product derivative isolated from a traditional Chinese herb. The aim of this study was to investigate the therapeutic effect of MSL in mice with collagen‐induced arthritis ( CIA ) and explore its underlying mechanism. Experimental Approach The anti‐arthritic effects of MSL were evaluated on human rheumatoid fibroblast‐like synoviocytes ( FLS ) in vitro and CIA in mice in vivo by obtaining clinical scores, measuring hind paw thickness and inflammatory cytokine levels, radiographic evaluations and histopathological assessments. Key Results Treatment with MSL after the onset of arthritis significantly prevented the progression and development of rheumatoid arthritis ( RA ) in CIA mice without megascopic gastric mucosa damage. In addition, MSL inhibited the production of pro‐inflammatory mediators, the phosphorylation and translocation of NF ‐κ B, and cell proliferation induced by TNF ‐α in FLS . MSL non‐selectively inhibited the activity of COX in vitro, but was a more potent inhibitor of COX‐2 than COX‐1. MSL also inhibited the phosphorylation of inhibitor of NF ‐κ B kinase, I κ B α and p65, thus blocking the nuclear translocation of NF ‐κ B in TNF ‐α‐stimulated FLS . Conclusion and Implications MSL exerts therapeutic effects on CIA mice, suppressing the inflammatory response and joint destruction by non‐selectively inhibiting the activity of COX and suppressing activation of the NF‐κB signalling pathway, but without damaging the gastric mucosa. Therefore, MSL has great potential to be developed into a novel therapeutic agent for the treatment of RA .