Rong Yumei, Hong Ge, Zhu Na, Liu Yang, Jiang Yong, Liu Tianjun
Tianjin Key Laboratory of Biomedical Material, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Department of Gastroenterology, The Second Hospital of Tianjin Medical University, Tianjin, China.
Front Pharmacol. 2021 Oct 21;12:746725. doi: 10.3389/fphar.2021.746725. eCollection 2021.
Ulcerative colitis (UC), a chronic, nonspecific inflammatory bowel disease characterized by continuous and diffuse inflammatory changes in the colonic mucosa, requires novel treatment method. Photodynamic therapy (PDT), as a promising physico-chemical treatment method, were used to treat UC rats' model with novel photosensitizer LD in this paper, the treatment effect and mechanism was investigated. LD-PDT could improve the survival rate of 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced UC model rats, decrease expression of interleukin (IL)-6, IL-1, tumor necrosis factor (TNF)-, malondialdehyde (MDA), myeloperoxidase (MPO) and increase the expression of glutathione (GSH) and superoxide oxidase (SOD), while protecting the integrity of the intestinal epithelium. LD-PDT treatment could rebuild the intestinal microflora composition and reprogram the colonic protein profiles in TNBS-induced rats to almost the normal state. Proteomics analysis based upon TNBS-induced UC model rats revealed that Amine oxidase copper-containing 1 (AOC) was a potential target of LD-PDT. Novel photosensitizer agent LD-PDT represents an efficient treatment method for UC, and AOC may be a promising target.
溃疡性结肠炎(UC)是一种慢性非特异性炎症性肠病,其特征为结肠黏膜出现连续性和弥漫性炎症改变,需要新的治疗方法。光动力疗法(PDT)作为一种有前景的物理化学治疗方法,本文采用新型光敏剂LD对UC大鼠模型进行治疗,并对其治疗效果及机制进行了研究。LD-PDT可提高2,4,6-三硝基苯磺酸(TNBS)诱导的UC模型大鼠的存活率,降低白细胞介素(IL)-6、IL-1、肿瘤坏死因子(TNF)-α、丙二醛(MDA)、髓过氧化物酶(MPO)的表达,并增加谷胱甘肽(GSH)和超氧化物歧化酶(SOD)的表达,同时保护肠上皮的完整性。LD-PDT治疗可使TNBS诱导的大鼠肠道微生物群组成重建,并使结肠蛋白质谱重新编程至几乎正常状态。基于TNBS诱导的UC模型大鼠的蛋白质组学分析表明,含铜胺氧化酶1(AOC)是LD-PDT的潜在靶点。新型光敏剂LD-PDT是一种治疗UC的有效方法,AOC可能是一个有前景的靶点。