Beijing National Laboratory for Molecular Sciences, Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Sci China Life Sci. 2022 Jun;65(6):1146-1156. doi: 10.1007/s11427-021-2001-0. Epub 2021 Nov 2.
Ulcerative colitis (UC) is a long-term, recurrent inflammatory bowel disease for which no effective cure is yet available in the clinical setting. Repairing the barrier dysfunction of the colon and reducing intestinal inflammation are considered key objectives to cure UC. Here we demonstrate a novel therapeutic strategy based on a C fullerene suspension (CFS) to treat dinitrobenzene sulfonic acid-induced UC in an animal model. CFS can repair the barrier dysfunction of UC and effectively promote the healing of ulcers; it also manifests better treatment effects compared with mesalazine enema. CFS can reduce the numbers of basophils in the blood of UC rats and mast cells in the colorectal tissue, thereby effectively alleviating inflammation. The expression of H1R, H4R, and VEGFR2 receptors in colorectal tissues is inhibited by CFS, and the levels of histamine and prostaglandin in the rat blood are reduced. This work presents a reliable strategy based on fullerene to cure UC and provides a novel guide for UC treatment.
溃疡性结肠炎(UC)是一种长期、反复发作的炎症性肠病,目前临床上尚无有效的治疗方法。修复结肠的屏障功能障碍和减轻肠道炎症被认为是治愈 UC 的关键目标。在这里,我们展示了一种基于 C60 富勒烯混悬液(CFS)的新型治疗策略,用于治疗动物模型中的二硝基苯磺酸诱导的 UC。CFS 可以修复 UC 的屏障功能障碍,有效促进溃疡愈合;与美沙拉嗪灌肠相比,它也表现出更好的治疗效果。CFS 可以减少 UC 大鼠血液中的嗜碱性粒细胞和结直肠组织中的肥大细胞数量,从而有效缓解炎症。CFS 抑制结直肠组织中 H1R、H4R 和 VEGFR2 受体的表达,降低大鼠血液中的组胺和前列腺素水平。这项工作提出了一种基于富勒烯治愈 UC 的可靠策略,为 UC 治疗提供了新的指导。