Copyright
©The Author(s) 2025.
World J Gastroenterol. Jun 21, 2025; 31(23): 106949
Published online Jun 21, 2025. doi: 10.3748/wjg.v31.i23.106949
Published online Jun 21, 2025. doi: 10.3748/wjg.v31.i23.106949
Figure 7 The effect of celastrol on NLR family pyrin domain containing 3 activation in vivo.
Data presented as mean ± SE. Statistical analysis was performed using Dunnett’s multiple comparison test, with the “vehicle” group as the control. A: Western blot analysis of NLR family pyrin domain containing 3 (NLRP3) and interleukin (IL)-1β in the esophageal ulceration area of rat tissues on day 6. aP < 0.001; bP < 0.001; cP = 0.004; dP = 0.01; eP < 0.001; fP = 0.01; B: mRNA levels of NLRP3 and IL-1β in rat esophagus on day 6. gP = 0.009; hP = 0.001; iP = 0.01; jP = 0.02; kP < 0.001; LP < 0.001; mP = 0.002; nP = 0.009; C: Representative immunohistochemistry (IHC) image of NLRP3 in the esophageal ulceration area of rats. Scale bar = 80 μm, 20 μm; D: Quantitative analysis of the NLRP3-positive area (%) for IHC, oP = 0.004; pP = 0.02; qP = 0.01; NLRP3: NLR family pyrin domain containing 3; CEL: Celastrol; PRED: Prednisolone; LPS: Lipopolysaccharide.
- Citation: Zhang MX, Wu C, Feng XX, Tian W, Zhao NH, Lu PP, Ding Q, Liu M. Celastrol alleviates esophageal stricture in rats by inhibiting NLR family pyrin domain containing 3 activation. World J Gastroenterol 2025; 31(23): 106949
- URL: https://www.wjgnet.com/1007-9327/full/v31/i23/106949.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i23.106949