Triptolide was intraperitoneally administrated every another day for 8 weeks to IL-10−/− mice. The gross and histological appearances of the colon, the level of inflammatory mediators and transcription factor activation in the colon were evaluated and compared with the control group.
The 8-week administration of triptolide resulted in a significant decrease in the severity of colitis, together with lower production of TNF-α ,IFN-γ and IL-4 in colon. The level of serum amyloid A was decreased in triptolide-treated mice. Gene expressions of IL-12 and IL-23 in colon were also downregulated after treatment. Furthermore, administration of triptolide markedly reduced NF-кB activation in colon mucosa of IL-10−/− mice.
The efficacy of tritpolide treatment for the reduction of intestinal inflammation in IL-10−/− mice is a result of both anti-inflammatory and immunosuppressive activity. Triptolide holds significant potential for clinical applications for CD treatment.