Copyright: ©Author(s) 2026.
World J Gastroenterol. Sep 7, 2026; 32(33): 117979
Published online Sep 7, 2026. doi: 10.3748/wjg.117979
Published online Sep 7, 2026. doi: 10.3748/wjg.117979
Figure 3 Naringenin pretreatment reduces inflammatory response and oxidative stress in hepatic ischemia-reperfusion injury.
A: Immunofluorescence staining images of CD11b+ cells in liver tissues; B: Quantitative analysis of CD11b+ positive cells (n = 3); C: MRNA expression levels of pro-inflammatory cytokines interleukin-1β (n = 3); D: MRNA expression levels of pro-inflammatory cytokines interleukin-6 (n = 3); E: MRNA expression levels of pro-inflammatory cytokines tumor necrosis factor-α (n = 3); F: Levels of malondialdehyde in liver tissue (n = 6); G: Levels of superoxide dismutase in liver tissue (n = 6); H: Levels of reduced glutathione in liver tissue (n = 6). Scale bar: 100 μm. aP < 0.05 vs the Sham group, bP < 0.05 vs the ischemia-reperfusion injury group. NAR: Naringenin; IRI: Ischemia-reperfusion injury; IL: Interleukin; TNF-α: Tumor necrosis factor-α; MDA: Malondialdehyde; SOD: Superoxide dismutase; GSH: Reduced glutathione.
- Citation: Lu JS, Liang HL, Chen DC, Pan H, Han T, Zhang WY, Fan M, Hou W, Shen ZY. Naringenin pretreatment attenuates hepatic ischemia-reperfusion injury by activating the PI3K-Akt signaling pathway. World J Gastroenterol 2026; 32(33): 117979
- URL: https://www.wjgnet.com/1007-9327/full/v32/i33/117979.htm
- DOI: https://dx.doi.org/10.3748/wjg.117979