肠道菌群
姜黄素
溃疡性结肠炎
势垒函数
结肠炎
微生物群
炎症性肠病
失调
炎症
代谢组学
胃肠道
医学
药理学
微生物学
生物
脂质运载蛋白
免疫学
化学
肠粘膜
氧化应激
平衡
紧密连接
粪便
短链脂肪酸
肠-脑轴
机制(生物学)
殖民抵抗
调解人
二十烷酸
丁酸盐
作者
Yin-zhuo Xie,Chen-Xi Sun,Tiantian Fu,Zheng Jin,Nonthaneth Nalinratana,Pornchai Rojsitthisak,Kai Zhao,Jingsheng Hua,Fangyi Pei,Xiaohua Wang
标识
DOI:10.1142/s0192415x26500837
摘要
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.
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