AI Article Synopsis

  • The study investigates how polysaccharides from Saposhnikovia divaricata (SDP) affect fibroblast-like synoviocytes (FLS) from a rat model of rheumatoid arthritis.
  • High concentrations of SDP significantly increased p53 gene expression and reduced inflammatory factors TNF-α and IL-1β, indicating its inhibitory effects on FLS.
  • Results showed that SDP treatment led to increased apoptosis in FLS by altering the balance of pro- and anti-apoptotic proteins, suggesting its potential as a therapeutic option for rheumatoid arthritis.

Article Abstract

To study the mechanism and inhibitory effect of Saposhnikovia divaricata polysaccharide (SDP) on fibroblast-like synoviocytes (FLS) isolated from rheumatoid arthritis rat model. Rheumatoid arthritis rat model was established by the classical composite factors including wind, cold, damp plus biological agents. The synovial tissues were digested with trypsin to isolate FLS cells. The different dosage of SDP was applied in culture. The cell viability was evaluated by MTT assay and the apoptosis was determined by analytic flow cytometry. The expression change of p53 gene was monitored by RT-PCR method. The production of secretory inflammation factors TNF-α and IL-1β were determined by ELISA. The proliferative and apoptotic proteins such as Bcl-2, Bax, Caspase-3, MMP-1, MMP-3, P53 were measured by western blotting. Our data demonstrated that treatment with high concentration of SDP could enhance the expression of P53 at both mRNA (P<0.05) and protein (P<0.05) level, inhibit the secretion of TNF-α (P<0.05) and IL-1β (P<0.05). Simultaneously, the Bcl-2/Bax ratio and level of MMP-1, MMP-3 was significantly decreased, and apoptotic marker caspase-3 protein was increased. In addition, the FACS analysis consistently consolidated the apoptosis-inducing effect of SDP on RAFLS. SDP could significantly inhibit dysplasia of RAFLS via modulation of p53 expression and suppression of inflammatory factors, which suggested a potential therapeutic value for rheumatoid arthritis.

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