Qiu Ting, Zhu Xiaodong, Wu Jingju, Hong Wenyuan, Hu Weitao, Fang Taiyong
Department of Gastroenterology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Department of General Practice, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, China.
Sci Rep. 2025 Mar 21;15(1):9815. doi: 10.1038/s41598-025-92282-4.
Metabolic dysfunction-associated steatohepatitis (MASH) has become a serious public health problem, posing an increasingly dangerous threat to human health owing to its increasing prevalence and accompanying intra- and extrahepatic adverse outcomes. Rifaximin is considered to have therapeutic potential for MASH; however, its efficacy remains controversial. Our study aimed to observe the ameliorative effects of rifaximin and explore its possible mechanisms at the cellular level. 1. 42 male C57BL/6J mice were divided into 3 groups, the CON group and MCD group were fed with normal feed and MCD feed for 12 weeks respectively, and the MCD + RFX group was treated with rifaximin by gavage for 4 weeks on the basis of MCD feed. Hematoxylin-eosin staining, Sirius red staining and immunohistochemical staining were used to observe the histopathological changes of liver and intestine. Differences in liver transaminases, inflammatory factors, fibrosis indexes and intestinal tight junction proteins were compared among the 3 groups of mice. 2. A MASH cell model was constructed by inducing HepG2 cells with free fatty acids to observe the effects of rifaximin on MASH in vitro. In addition, the effects of rifaximin on TLR4/NF-κB signaling pathway were explored by applying TLR4 agonist LPS and TLR4 inhibitor TAK-242. Hepatic histopathology was significantly improved in MASH mice after rifaximin treatment, and their serum alanine aminotransferase and aspartate aminotransferase levels were (72.72 ± 5.68) U/L and (222.8 ± 11.22) U/L, respectively, which were significantly lower than those in the MCD group [(293.3 ± 10.69) U/L and (414.1 ± 36.29) U/L, P < 0.05], and the levels of inflammatory factors and fibrosis indicators were reduced. Rifaximin ameliorated intestinal barrier injury with increased expression of intestinal tight junction protein ZO-1 in the MCD + RFX group of mice, and the concentration of LPS-binding proteins (4.92 ± 0.55 vs. 15.82 ± 1.71, P < 0.05) was lower than that in the MCD group. In the NASH cell model, rifaximin similarly exerted inhibitory effects on its inflammatory factors and TLR4/NF-κB signaling pathway. Application of TLR4 inhibitors weakened the inhibitory effect of rifaximin on MASH. Our study supports rifaximin as a potential treatment for MASH, with potential mechanisms related to improving intestinal barrier integrity and downregulating the TLR4/NF-κB signaling pathway.
代谢功能障碍相关脂肪性肝炎(MASH)已成为一个严重的公共卫生问题,由于其患病率不断上升以及伴随的肝内和肝外不良后果,对人类健康构成了日益严重的威胁。利福昔明被认为对MASH具有治疗潜力;然而,其疗效仍存在争议。我们的研究旨在观察利福昔明的改善作用,并在细胞水平上探索其可能的机制。1. 将42只雄性C57BL/6J小鼠分为3组,CON组和MCD组分别给予正常饲料和MCD饲料喂养12周,MCD + RFX组在MCD饲料基础上通过灌胃给予利福昔明治疗4周。采用苏木精-伊红染色、天狼星红染色和免疫组织化学染色观察肝脏和肠道的组织病理学变化。比较3组小鼠肝转氨酶、炎症因子、纤维化指标和肠道紧密连接蛋白的差异。2. 通过用游离脂肪酸诱导HepG2细胞构建MASH细胞模型,以观察利福昔明在体外对MASH的影响。此外,通过应用TLR4激动剂LPS和TLR4抑制剂TAK-242探索利福昔明对TLR4/NF-κB信号通路的影响。利福昔明治疗后,MASH小鼠的肝脏组织病理学明显改善,其血清丙氨酸转氨酶和天冬氨酸转氨酶水平分别为(72.72±5.68)U/L和(222.8±11.22)U/L,显著低于MCD组[(293.3±10.69)U/L和(414.1±36.29)U/L,P<0.05],炎症因子和纤维化指标水平降低。利福昔明改善了肠道屏障损伤,MCD + RFX组小鼠肠道紧密连接蛋白ZO-1的表达增加,脂多糖结合蛋白浓度(4.92±0.55对15.82±1.71,P<0.05)低于MCD组。在NASH细胞模型中,利福昔明同样对其炎症因子和TLR4/NF-κB信号通路发挥抑制作用。应用TLR4抑制剂减弱了利福昔明对MASH的抑制作用。我们的研究支持利福昔明作为MASH的一种潜在治疗方法,其潜在机制与改善肠道屏障完整性和下调TLR4/NF-κB信号通路有关。