Zhao Man, Liu Mengqi, Wu Fengyang, Li Chong, Liu Shudong, Yang Xinyu, Wei Zhonghua, Chen Baojiang, Han Shuaijuan
College of Animal Science and Technology, Hebei Agricultural University, Baoding 071000, China.
College of Animal Science and Technology, Henan Agricultural University, Zhengzhou 450002, China.
J Agric Food Chem. 2025 Jul 2;73(26):16317-16332. doi: 10.1021/acs.jafc.5c00220. Epub 2025 Jun 17.
Ursolic acid (UA), a natural compound abundant in fruits and vegetables, exhibits established anti-inflammatory and hepatoprotective properties. This study investigated the therapeutic potential of UA as a dietary supplement for DSS-induced colitis and secondary liver injury using both an DSS-induced colitis mouse model and an intestinal epithelial cell model. Colitis model mice were administered UA at doses of 5, 25, 100, and 250 mg/kg. Through comprehensive analyses, including enzyme-linked immunosorbent assay (ELISA), immunohistochemistry (IHC), immunofluorescence (IF), Western blot, 16S rRNA sequencing, untargeted metabolomics, and transcriptomics, we demonstrated that 25 mg/kg UA optimally alleviated colitis symptoms. The mechanism involves restoring the balance between T regulatory cells (Treg) and T helper 17 cells (Th17) to reduce inflammation, potentially mediated by increased production of propionate from short-chain fatty acid (SCFA)-producing bacteria. Additionally, UA inhibits () growth through the action of the microbial metabolite l-histidine, thereby enhancing intestinal barrier integrity and inhibiting pyroptosis. Moreover, 25 mg/kg of UA exerts protective effects against liver injury by suppressing inflammation-related signaling pathways in colitis mice. These findings position UA as a promising functional food component for managing colitis and its hepatic complications.
熊果酸(UA)是一种在水果和蔬菜中大量存在的天然化合物,具有已被证实的抗炎和肝脏保护特性。本研究使用DSS诱导的结肠炎小鼠模型和肠上皮细胞模型,研究了UA作为膳食补充剂对DSS诱导的结肠炎和继发性肝损伤的治疗潜力。给结肠炎模型小鼠分别给予5、25、100和250mg/kg剂量的UA。通过包括酶联免疫吸附测定(ELISA)、免疫组织化学(IHC)、免疫荧光(IF)、蛋白质印迹法、16S rRNA测序、非靶向代谢组学和转录组学在内的综合分析,我们证明25mg/kg的UA能最佳地缓解结肠炎症状。其机制包括恢复调节性T细胞(Treg)和辅助性T细胞17(Th17)之间的平衡以减轻炎症,这可能是由产生短链脂肪酸(SCFA)的细菌增加丙酸生成所介导的。此外,UA通过微生物代谢产物L-组氨酸的作用抑制()生长,从而增强肠道屏障完整性并抑制细胞焦亡。此外,25mg/kg的UA通过抑制结肠炎小鼠中与炎症相关的信号通路,对肝损伤发挥保护作用。这些发现表明UA是一种有前景的功能性食品成分,可用于管理结肠炎及其肝脏并发症。