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
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI