©The Author(s) 2025.
World J Gastroenterol. Sep 21, 2025; 31(35): 108139
Published online Sep 21, 2025. doi: 10.3748/wjg.v31.i35.108139
Published online Sep 21, 2025. doi: 10.3748/wjg.v31.i35.108139
Figure 5 Ambroxol suppressed inflammation in cyclophosphamide-treated rats.
A-C: Ambroxol decreased liver toll-like receptor-4 (A and B), nuclear factor-kappaB (NF-κB) p65 (A and C); D: Tumor necrosis factor-α; E: Interleukin-1β. Data are expressed as mean ± SD (n = 6). bP < 0.01 and cP < 0.001 vs control group, eP < 0.01 and fP < 0.001 vs cyclophosphamide. ABX: Ambroxol; CP: Cyclophosphamide; TLR: Toll-like receptor; NF-κB: Nuclear factor-kappa B; TNF: Tumor necrosis factor; IL: Interleukin.
- Citation: Alruhaimi RS, Hassanein EHM, Alnasser SM, Ahmeda AF, Althagafy HS, Abd El-Ghafar OAM, Mahmoud AM. Ambroxol mitigates cyclophosphamide-induced liver injury by suppressing TLR-4/NF-κB signaling and oxidative stress and upregulating cytoglobin, TXNRD1 and HMGB1. World J Gastroenterol 2025; 31(35): 108139
- URL: https://www.wjgnet.com/1007-9327/full/v31/i35/108139.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i35.108139