Copyright: ©Author(s) 2026.
World J Gastroenterol. Jun 21, 2026; 32(23): 117320
Published online Jun 21, 2026. doi: 10.3748/wjg.v32.i23.117320
Published online Jun 21, 2026. doi: 10.3748/wjg.v32.i23.117320
Figure 12 Esmolol ameliorates lipopolysaccharide-induced intestinal injury via the AMPK/mTOR/ULK1 autophagy pathway.
A: The MTT assay was used to detect cell viability; B-D: Western blotting analysis was performed to analyze Beclin-1, LC3-II expression in IEC-6 cells in the Sham, lipopolysaccharide (LPS), LPS + esmolol (ES), LPS + Compound C (CC), and LPS + ES + CC treatment groups (after 6 hours of treatment); E-H: Western blotting analysis was performed to analyze p-AMPK, p-ULK1, and p-mTOR expression in IEC-6 cells after 6 hours of treatment in each group. β-actin was used as a loading control and for normalization. Representative immunoblots and densitometry analyses are presented. Data in the Sham group were set to 1. n = 6 in each group. ES: Esmolol; CC: Compound C; LPS: Lipopolysaccharide.
- Citation: Zhang YB, Yu ZJ, Jin J, Liu MX, Ji FH, Yang XJ. Esmolol alleviates lipopolysaccharide-induced intestinal injuries by enhancing autophagy through the AMPK/mTOR/ULK1 pathway. World J Gastroenterol 2026; 32(23): 117320
- URL: https://www.wjgnet.com/1007-9327/full/v32/i23/117320.htm
- DOI: https://dx.doi.org/10.3748/wjg.v32.i23.117320