Abstract
Eucommia ulmoides Oliv., a native Chinese plant species, has been used as a traditional Chinese medicine formulation to treat rheumatoid arthritis (RA), strengthen bones and muscles, and lower blood pressure. Various parts of this plant such as the bark, leaves, and flowers have been found to have anti-inflammatory properties. E. ulmoides has potential applications as a therapeutic agent against bone disorders, which were investigated in this study. In vitro, RA joint fibroblast-like synoviocytes (RA-FLS) were treated with different concentrations (0, 25, 50, 100, 200, 400, 800, and 1000 μg/mL) of E. ulmoides bark, leaf, and male flower alcoholic extracts (EB, EL, and EF, respectively) to determine their potential cytotoxicity. Tumor necrosis factor- (TNF-) α and nitric oxide (NO) levels in RA-FLS were quantified using enzyme-linked immunosorbent assay (ELISA). Furthermore, collagen-induced arthritis (CIA) rats were treated with EB, EL, EF, Tripterygium wilfordii polyglycoside (TG) or the normal control (Nor), and then ankle joint pathology, bone morphology, and serum and spleen inflammatory cytokine levels were evaluated. The results showed that, in RA-FLS, EB, EL, and EF were not cytotoxic; EB and EF reduced TNF-α supernatant levels; and EB, EL, and EF reduced NO levels. The results of in vivo experiments showed that EB, EL, and EF alleviated ankle swelling and joint inflammation, while all extracts diminished inflammatory cell infiltration, pannus and bone destruction, and bone erosion. All tested extracts inhibited interleukin- (IL-) 6, IL-17, and TNF-α mRNA in the spleen of CIA rats, while EB most effectively reduced osteoclasts and inhibited bone erosion. EF showed the most obvious inhibition of inflammatory factors and pannus. Thus, EB, EL, and EF may alleviate bone destruction by inhibiting inflammation.
Highlights
Rheumatoid arthritis (RA) is a chronic autoimmune disease mainly characterized by synovial inflammation and bone destruction [1]
Different concentrations of EB, EL, and EF exhibited no inhibitory effects on RA joint fibroblast-like synoviocytes (RA-Fibroblast-like synoviocytes (FLS)) cells, indicating that concentrations up to 1000 μg/mL were not cytotoxic (Figure 1(a)). erefore, experimental groups treated with 500 μg/mL were analyzed for effects on tumor necrosis factor- (TNF-)α and nitric oxide (NO) levels of synovial extracellular fluid
Results showed that TNF-α expression of the cell-culture supernatants of the EB, EF, and Tripterygium wilfordii polyglycoside (TG) groups decreased significantly (P < 0.05) compared to that of the negative control group, while NO expression levels in the cell culture supernatants of the EB, EL, EF, and TG groups decreased significantly (P < 0.01) compared to those of the negative control group (Figure 1(b))
Summary
Rheumatoid arthritis (RA) is a chronic autoimmune disease mainly characterized by synovial inflammation and bone destruction [1]. Fibroblast-like synoviocytes (FLS) in normal synovial tissues maintain normal joint function by producing extracellular matrix components and joint lubricants. In RA, FLS can be induced by immunopathological mechanisms and signal transduction to synthesize numerous factors that mediate inflammation and joint damage [2]. Inflammatory cytokines including tumor necrosis factor- (TNF-) α, interleukin- (IL-) 1β, IL-6, and IL-17 play a critical role in the pathogenesis of RA. TNF-α, IL-1β, and IL-17 induce RA synovitis with the promotion of vasospasm and cause bone destruction in late-stage synovitis [3]. Four main approaches are used for the treatment of RA: nonsteroidal anti-inflammatory drugs, disease-modifying antirheumatic drugs, glucocorticoids, and herbal preparations [4].
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