Nanoformulated Curcumin Ameliorates Ulcerative Colitis via Gut Microbiota Modulation and Barrier Function Restoration.

IF 5.5
Yin-Zhuo Xie, Chen-Xi Sun, Tian-Tian Fu, Zheng Jin, Nonthaneth Nalinratana, Pornchai Rojsitthisak, Kai Zhao, Jing-Sheng Hua, Fang-Yi Pei, Xiao-Hua Wang
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Abstract

The gut microbiota is increasingly recognized as a key mediator of the anticolitis effects of curcumin (CUR). However, the clinical translation of this promising activity is severely hampered by CUR's low solubility and poor bioavailability. Although nanoencapsulation represents a promising strategy to address these limitations, the preventive effect of nanocurcumin (nano-CUR) against colitis remains largely unexplored. The present study aimed to elucidate the preventive effects of nano-CUR on intestinal barrier function, gut microbiota composition, and metabolic profiles in a murine model of dextran sulfate sodium (DSS)-induced colitis. The results demonstrated that pre-supplementation of nano-CUR significantly ameliorated disease severity, attenuated intestinal barrier disruption, and suppressed colonic inflammation in mice with DSS-induced colitis. Mechanistically, integrated 16S rRNA sequencing and untargeted metabolomics demonstrated that nano-CUR-restored microbial homeostasis and enhanced the production of short-chain fatty acids, linking microbial shifts to anti-inflammatory outcomes. Fecal microbiota transplantation (FMT) further validated the causal role of the nano-CUR-remodeled microbiota in conferring protection. Collectively, these findings decipher the mechanism by which nano-CUR interacts with the gut microbiota, confirming that dietary nano-CUR consumption protects against ulcerative colitis by modulating the gut microbiome and its metabolic output.

纳米姜黄素通过肠道菌群调节和屏障功能恢复改善溃疡性结肠炎。
肠道微生物群越来越被认为是姜黄素(CUR)抗结肠炎作用的关键媒介。然而,这种有希望的活性的临床转化受到CUR的低溶解度和生物利用度差的严重阻碍。尽管纳米胶囊化是解决这些局限性的一种很有前途的策略,但纳米姜黄素(nano-CUR)对结肠炎的预防作用仍未得到充分研究。本研究旨在阐明纳米cur对小鼠右旋糖酐硫酸钠(DSS)诱导的结肠炎模型中肠道屏障功能、肠道微生物群组成和代谢谱的预防作用。结果表明,预先补充纳米cur可显著改善dss诱导结肠炎小鼠的疾病严重程度,减轻肠屏障破坏,并抑制结肠炎症。在机制上,集成16S rRNA测序和非靶向代谢组学表明,纳米cu恢复了微生物稳态,增强了短链脂肪酸的产生,将微生物变化与抗炎结果联系起来。粪便微生物群移植(FMT)进一步验证了纳米cu重塑的微生物群在赋予保护作用中的因果作用。总的来说,这些发现破译了纳米cur与肠道微生物群相互作用的机制,证实了饮食中纳米cur的摄入通过调节肠道微生物群及其代谢输出来预防溃疡性结肠炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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