Department of Colorectal and Anal Surgery, The First Affiliated Hospital of College of Medicine, Zhejiang University, China.
College of Life Science, Sichuan Normal University, Chengdu, Sichuan 610101, China.
J Immunol Res. 2021 Apr 30;2021:6679316. doi: 10.1155/2021/6679316. eCollection 2021.
Ulcerative colitis (UC) is a chronic and relapsing inflammatory bowel disorder in the colon and rectum leading to low life-quality and high societal costs. Ursolic acid (UA) is a natural product with pharmacological and biological activities. The studies are aimed at investigating the protective and treatment effects of UA against the dextran sulfate sodium- (DSS-) induced UC mouse model and its underlying mechanism. UA was orally administered at different time points before and after the DSS-induced model. Mice body weight, colon length, and histological analysis were used to evaluate colon tissue damage and therapeutic evaluation. Intestinal transcriptome and microbe 16 s sequencing was used to analyze the mechanisms of UA in the prevention and treatment of UC. The early prevention effect of UA could effectively delay mouse weight loss and colon length shorten. UA alleviated UC inflammation and lowered serum and colon IL-6 levels. Three classical inflammatory pathways: MAPKs, IL-6/STAT3, and PI3K were downregulated by UA treatment. The proportion of macrophages and neutrophils in inflammatory cell infiltration was reduced in UA treatment groups. UA could significantly reduce the richness of intestinal flora to avoid the inflammatory response due to the destruction of the intestinal epithelial barrier. The function of UA against UC was through reducing intestinal flora abundance and regulating inflammatory and fatty acid metabolism signaling pathways to affect immune cell infiltration and cytokine expression.
溃疡性结肠炎(UC)是一种慢性、复发性的结肠和直肠炎症性肠病,导致生活质量降低和社会成本增加。熊果酸(UA)是一种具有药理和生物学活性的天然产物。本研究旨在探讨 UA 对葡聚糖硫酸钠(DSS)诱导的 UC 小鼠模型的保护和治疗作用及其机制。UA 在 DSS 诱导模型前后的不同时间点进行口服给药。采用小鼠体重、结肠长度和组织学分析来评估结肠组织损伤和治疗评估。肠道转录组和微生物 16s 测序用于分析 UA 在预防和治疗 UC 中的作用机制。UA 的早期预防作用可有效延缓小鼠体重减轻和结肠缩短。UA 减轻 UC 炎症并降低血清和结肠 IL-6 水平。UA 治疗可下调三个经典炎症通路:MAPKs、IL-6/STAT3 和 PI3K。UA 治疗组炎症细胞浸润中巨噬细胞和中性粒细胞的比例降低。UA 可显著降低肠道菌群的丰富度,避免因肠道上皮屏障破坏引起的炎症反应。UA 对 UC 的作用是通过减少肠道菌群丰度和调节炎症及脂肪酸代谢信号通路,影响免疫细胞浸润和细胞因子表达。