Wang Ke-Ying, Huang Chun-Xiang, Hu Xiao-Jia, Liu Jun-Yang, Qin Xiao-Hui, Tong Chen-Xi, Liu Zhi-Qiang, He Wen, Jiang Tie-Min, Song Jia-Le
Guangxi Key Laboratory of Environmental Exposureomics and Entire Lifecycle Health, Guilin Medical University, No. 1, Zhiyuan Road, Guangxi, Guilin 541100, China.
South Asia Branch of National Engineering Center of Dairy for Maternal and Child Health, Guilin University of Technology, No. 319, Yanshan Street, Guangxi, Guilin 541004, China.
ACS Omega. 2025 Sep 5;10(36):40981-40994. doi: 10.1021/acsomega.5c03232. eCollection 2025 Sep 16.
The development of strictures due to intestinal fibrosis remains a significant clinical challenge in patients with ulcerative colitis (UC). The purpose of this experiment was to investigate the protective effects of naringenin (NAR, 40 mg/kg), a natural flavonoid predominantly present in grapes and oranges, against dextran sodium sulfate (DSS, 2.5%)-induced intestinal fibrosis in UC mice. Oral administration of NAR effectively mitigated clinical symptoms and histological damage in UC mice by reducing the colonic F4/80 and MPO levels. Additionally, NAR lowered the serum concentrations of proinflammatory cytokines and inhibited NLRP3 inflammasome activation in the colon. NAR regulates the Nrf2/Keap1 pathway to combat oxidative damage caused by DSS and enhance autophagy through the AMPK-Akt/mTOR pathway, ultimately decreasing intestinal fibrosis in UC mice by inhibiting α-SMA and Collagen-I. Taken together, our findings demonstrate that NAR can prevent the occurrence and progression of intestinal fibrosis. This effect is achieved by adjusting the AMPK-Akt/mTOR pathway and the promotion of autophagy at the molecular level.
溃疡性结肠炎(UC)患者中,因肠道纤维化导致的狭窄形成仍是一项重大的临床挑战。本实验旨在研究柚皮素(NAR,40毫克/千克)对葡聚糖硫酸钠(DSS,2.5%)诱导的UC小鼠肠道纤维化的保护作用,柚皮素是一种主要存在于葡萄和橙子中的天然黄酮类化合物。口服NAR可通过降低结肠F4/80和MPO水平,有效减轻UC小鼠的临床症状和组织学损伤。此外,NAR降低了促炎细胞因子的血清浓度,并抑制了结肠中NLRP3炎性小体的激活。NAR通过调节Nrf2/Keap1途径对抗DSS引起的氧化损伤,并通过AMPK-Akt/mTOR途径增强自噬,最终通过抑制α-SMA和I型胶原蛋白减少UC小鼠的肠道纤维化。综上所述,我们的研究结果表明,NAR可以预防肠道纤维化的发生和进展。这种作用是通过在分子水平上调节AMPK-Akt/mTOR途径和促进自噬来实现的。