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姜黄素与色氨酸联合使用通过减轻炎症和氧化应激以及调节肠道微生物群来改善右旋糖酐硫酸钠诱导的溃疡性结肠炎。

Curcumin Combined with Tryptophan Ameliorates DSS-Induced Ulcerative Colitis via Reducing Inflammation and Oxidative Stress and Regulation of Gut Microbiota.

作者信息

Jiang Hedong, Li Gonglong, Xie Liuming, Zhang Nanhai, Huang Yi, Liang Xinli, Guo Fanghua, Jiang Qieying, Liao Zhenggen

机构信息

Key Laboratory of Modern Preparation of TCM, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

School of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

出版信息

Nutrients. 2025 Sep 18;17(18):2988. doi: 10.3390/nu17182988.

DOI:10.3390/nu17182988
PMID:41010513
Abstract

: Curcumin (Cur) and tryptophan (Trp) both show promise for treating ulcerative colitis (UC) alone, but their combination has not been explored. This study investigated the therapeutic advantage of the combination (Cur-Trp) for DSS-induced ulcerative colitis in mice. : We established a mouse model of ulcerative colitis induced by dextran sulfate sodium (DSS). The mice were treated with Cur, Trp, or Cur-Trp, and to evaluate the therapeutic effects, we assessed clinical signs such as body weight, disease activity index (DAI), and colon length. We also examined intestinal barrier function through indicators including histopathological changes, inflammatory factors, oxidative stress levels, mucin secretion, and tight junction protein expression. Additionally, we analyzed the composition of gut microbiota and the content of its metabolites like short-chain fatty acids (SCFAs). : The Cur-Trp group produced the most significant improvement, exceeding that of Cur or Trp group. This was evidenced by a significant recovery of this sign, including slower weight loss, reduced colon shortening, and de-creased disease activity index. Compared with the model group, the weight loss of mice in the Cur-Trp group was reduced from 17.15% to 9.73%, which was better than that in the cur group (11.33%) and the Trp group (11.59%). The DAI decreased from the model group (3.6) to the Cur-Trp group (2.4), while the DAI in the Cur group and the Trp group only decreased to 2.9 and 2.8, respectively. The colon length in the Cur-Trp group (6.52 cm) was larger than that in the cur group (6.31 cm), the Trp group (6.23 cm) and the model group (5.5 cm). The Cur-Trp intervention effectively restored intestinal barrier function, as shown by reducing colon tissue dam-age, modulating inflammatory factors, restoring oxidative balance, increasing mucin secretion, and upregulating tight junction protein expression. Further studies showed that the combination uniquely modulated the gut microbiome, increased the Firmicutes/Bacteroidetes (F/B) ratio, decreased the genus of pro-inflammatory bacteria, and in-creased beneficial bacteria, while increasing SCFA levels to alleviate DSS-induced ulcerative colitis. : Cur-Trp has shown great potential in alleviating colitis and promoting intestinal barrier function, suggesting that the combination of Cur and Trp has the potential to be developed as a therapeutic functional food or dietary supplement for UC. However, more studies are needed to validate this finding. Future research should focus on elucidating the precise molecular mechanisms, optimizing dosage and clinical trials in chronic models and humans to provide more targeted treatment options.

摘要

姜黄素(Cur)和色氨酸(Trp)单独治疗溃疡性结肠炎(UC)均显示出前景,但它们的联合应用尚未得到探索。本研究调查了联合用药(Cur-Trp)对葡聚糖硫酸钠(DSS)诱导的小鼠溃疡性结肠炎的治疗优势。

我们建立了葡聚糖硫酸钠诱导的溃疡性结肠炎小鼠模型。小鼠分别接受Cur、Trp或Cur-Trp治疗,为评估治疗效果,我们评估了体重、疾病活动指数(DAI)和结肠长度等临床指标。我们还通过组织病理学变化、炎症因子、氧化应激水平、粘蛋白分泌和紧密连接蛋白表达等指标检测肠道屏障功能。此外,我们分析了肠道微生物群的组成及其代谢产物如短链脂肪酸(SCFAs)的含量。

Cur-Trp组改善最为显著,超过了Cur组或Trp组。这体现在各项指标的显著恢复,包括体重减轻减缓、结肠缩短减轻以及疾病活动指数降低。与模型组相比,Cur-Trp组小鼠体重减轻从17.15%降至9.73%,优于Cur组(11.33%)和Trp组(11.59%)。DAI从模型组的3.6降至Cur-Trp组的2.4,而Cur组和Trp组的DAI仅分别降至2.9和2.8。Cur-Trp组的结肠长度(6.52 cm)大于Cur组(6.31 cm)、Trp组(6.23 cm)和模型组(5.5 cm)。Cur-Trp干预有效恢复了肠道屏障功能,表现为减少结肠组织损伤、调节炎症因子、恢复氧化平衡、增加粘蛋白分泌以及上调紧密连接蛋白表达。进一步研究表明,联合用药独特地调节了肠道微生物群,增加了厚壁菌门/拟杆菌门(F/B)比值,减少了促炎细菌属,增加了有益细菌,同时提高了SCFA水平以缓解DSS诱导的溃疡性结肠炎。

Cur-Trp在缓解结肠炎和促进肠道屏障功能方面显示出巨大潜力,表明Cur和Trp的联合有潜力开发为UC的治疗功能性食品或膳食补充剂。然而,需要更多研究来验证这一发现。未来的研究应集中于阐明精确的分子机制,优化剂量,并在慢性模型和人类中进行临床试验,以提供更有针对性的治疗选择。

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