Oral administration of nanoformulated indoximod ameliorates ulcerative colitis by promoting mitochondrial function and mucosal healing

溃疡性结肠炎 芳香烃受体 炎症 炎症性肠病 药理学 结肠炎 势垒函数 化学 封堵器 肠粘膜 医学 代谢物 线粒体ROS 线粒体 紧密连接 癌症研究 免疫学 病理 内科学 生物 生物化学 细胞生物学 疾病 基因 转录因子
作者
Peiyao Wu,Siyu Yao,Xing Wang,Long Yang,Siling Wang,Wenbing Dai,Hua Zhang,Bing He,Xueqing Wang,Shujun Wang,Qiang Zhang
出处
期刊:International Journal of Pharmaceutics [Elsevier]
卷期号:637: 122813-122813 被引量:7
标识
DOI:10.1016/j.ijpharm.2023.122813
摘要

Ulcerative colitis (UC) is a chronic relapsing inflammatory bowel disease with serious mucosal inflammation mainly in the colon and rectum. Currently, there is no effective therapeutics for UC. Indoximod (IND) is a water-insoluble inhibitor for indolamine 2, 3-dioxygenase (IDO) and has been mainly reported in cancer therapy. Here, we prepared orally administrated IND nanoparticles (IND-NPs) for UC treatment and investigated their functions and mechanisms in cellular and animal inflammatory models. Confocal imaging demonstrated that IND-NPs maintained the expression level of ZO-1, Occludin and E-cadherin, thereby stabilizing of intercellular junction in Caco-2 cells. It was found that IND-NPs could lower the ROS level and increase mitochondrial membrane potential as well as ATP level, indicating that IND-NPs could restore DSS-induced mitochondrial dysfunction. In the mice model with DSS-induced colitis, IND-NPs were found to alleviate UC-associated symptoms, inhibit inflammatory response, and improve the integrity of epithelial barrier. The untargeted metabolomics analysis validated that IND-NPs also contributed to regulate the metabolite levels to normal. As an agonist of aryl hydrocarbon receptor (AhR), IND-NPs might repair mucosa via the AhR pathway. These findings demonstrated that IND-NPs prominently ameliorated DSS-induced colonic injury and inflammation and preserved intestinal barrier integrity, showing a promising potential in UC treatment.
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