Copyright: ©Author(s) 2026.
World J Gastroenterol. May 7, 2026; 32(17): 116590
Published online May 7, 2026. doi: 10.3748/wjg.v32.i17.116590
Published online May 7, 2026. doi: 10.3748/wjg.v32.i17.116590
Figure 9 Farnesoid X receptor inhibitor abolishes the therapeutic effects of the Niu Huang.
A: Representative images of the colon length; B: Colon length (n = 4 in each group); C and D: Protein expression levels of NOD-like receptor family pyrin domain containing 3, complement component 3, p-P65 and P65 in colon tissues (n = 4 in each group); E: Representative images of the colon length; F: Colon length (n = 6 in each group); G: Disease active index; H: Representative hematoxylin and eosin staining images of colon tissues. aP < 0.05 vs dextran sulfate sodium group, bP < 0.01 vs dextran sulfate sodium group. WT: Wild type; DSS: Dextran sulfate sodium; FXR: Farnesoid X receptor; C3: Complement component 3; NLRP3: NOD-like receptor family pyrin domain containing 3; Gug: Gug gulsterone; NH: Niu Huang.
- Citation: Shi J, Ma CY, Zhang XH, Liu KJ, Liu JY, Wang QG, Wang XQ, Cheng FF, Xu T. Niu Huang mitigates dextran sulfate sodium-induced colitis by modulating farnesoid X receptor activation and the complement 3/NLRP3 signaling pathway. World J Gastroenterol 2026; 32(17): 116590
- URL: https://www.wjgnet.com/1007-9327/full/v32/i17/116590.htm
- DOI: https://dx.doi.org/10.3748/wjg.v32.i17.116590