Department of Pharmaceutics, College of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China; Beijing Key Laboratory of Molecular Pharmaceutics, New Drug Delivery Systems, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Beijing Key Laboratory of Molecular Pharmaceutics, New Drug Delivery Systems, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Int J Pharm. 2023 Apr 25;637:122813. doi: 10.1016/j.ijpharm.2023.122813. Epub 2023 Mar 9.
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.
溃疡性结肠炎(UC)是一种慢性复发性炎症性肠病,主要累及结肠和直肠的黏膜炎症。目前,UC 尚无有效的治疗方法。Indoximod(IND)是一种不溶于水的吲哚胺 2,3-双加氧酶(IDO)抑制剂,主要用于癌症治疗。本研究制备了可口服的 IND 纳米粒(IND-NPs)用于治疗 UC,并在细胞和动物炎症模型中研究了其功能和机制。共聚焦成像显示,IND-NPs 维持了 ZO-1、Occludin 和 E-cadherin 的表达水平,从而稳定了 Caco-2 细胞的细胞间连接。研究发现,IND-NPs 可以降低 ROS 水平,增加线粒体膜电位和 ATP 水平,表明 IND-NPs 可以恢复 DSS 诱导的线粒体功能障碍。在 DSS 诱导的结肠炎小鼠模型中,IND-NPs 可减轻 UC 相关症状、抑制炎症反应,并改善上皮屏障的完整性。非靶向代谢组学分析验证了 IND-NPs 还可以调节代谢物水平至正常。作为芳烃受体(AhR)的激动剂,IND-NPs 可能通过 AhR 途径修复黏膜。这些发现表明,IND-NPs 显著改善了 DSS 诱导的结肠损伤和炎症,并维持了肠道屏障的完整性,在 UC 治疗方面具有广阔的应用前景。