法尼醇通过调节炎症细胞因子、修复肠道屏障、逆转肠道微生物群失衡以及影响 C57BL/6 小鼠粪便代谢组,改善了 DSS 诱导的 IBD。

Ya Yuan, Dazuo Wu, Heping Chen, Zheng Ma, Xinyue Peng, Xiaodie Li, Chuchu Zhao, Linping Jiang, Jinping Liang, Weiwei Zhang, Juan Dai
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引用次数: 0

摘要

炎症性肠病(IBD)的发病率在全球范围内呈上升趋势,因此人们对用于预防和控制该病的食品成分越来越感兴趣。本研究评估了柚子花挥发油的主要成分法尼醇(FAR)对右旋糖酐硫酸钠(DSS)诱导的 C57BL/6 小鼠结肠炎的影响。柚子花挥发油明显减轻了右旋糖酐硫酸钠(DSS)诱导的结肠炎和继发性肝损伤,表现为体重、DAI、结肠长度和病理变化以及肝功能和血脂指标的改善。其机制涉及 FAR 介导的炎症细胞因子调节、紧密连接蛋白基因表达的增加和脂质代谢相关蛋白表达的减少。FAR 还提高了肠道微生物群的多样性,平衡了有害菌和益生菌。粪便代谢组分析表明,FAR 在逆转与炎症和肝脏脂质代谢有关的代谢紊乱方面发挥了作用。这些研究结果支持利用柚子花挥发油开发治疗 IBD 的功能性食品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Farnesol ameliorates DSS-induced IBD by regulating inflammatory cytokines, repairing the intestinal barrier, reversing the gut microbiota imbalance, and influencing fecal metabolome in C57BL/6 mice.

The incidence of inflammatory bowel disease (IBD) is rising globally, increasing interest in food ingredients for its prevention and control. This study evaluated the effect of farnesol (FAR), a key component of pomelo flower volatile oil, on dextran sodium sulfate (DSS)-induced colitis in C57BL/6 mice. FAR significantly alleviated DSS-induced colitis and secondary liver injury, as shown by improved body weight, DAI, colon length, and pathology, as well as liver function and blood lipid indices. The mechanism involves FAR-mediated regulation of inflammatory cytokines, increased expression of tight junction protein genes, and decreased expression of lipid metabolism-related proteins. FAR also enhanced gut microbiota diversity, balancing harmful and probiotic bacteria. Fecal metabolome analysis indicated FAR's role in reversing metabolic disturbances related to inflammation and liver lipid metabolism. These findings support developing functional foods for IBD treatment using pomelo flower volatile oil.

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