Kim Dongwoo, Koo Ja Seol, Kim Soon Ha, Park Yeong Seo, Choe Jung Wan, Kim Seung Young, Hyun Jong Jin, Jung Sung Woo, Jung Young Kul, Yim Hyung Joon
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Ansan Hospital, Korea University College of Medicine, Seoul 02841, Republic of Korea.
MitoImmune Therapeutics Inc., Seoul 06123, Republic of Korea.
Pharmaceutics. 2023 Jan 9;15(1):222. doi: 10.3390/pharmaceutics15010222.
Uncontrolled chronic inflammation and necrosis is characteristic of inflammatory bowel disease (IBD). This study aimed to investigate the effect of necrosis inhibitor (NI, NecroX-7) on a dextran sulfate sodium (DSS) induced chronic colitis model of mice. DSS was administered on days 1-5, and the NI was administered intraperitoneally (3 mg/kg, 30 mg/kg) on days 1, 3, and 5 as well as every other day during the first five days of a three-week cycle. Three cycles of administration were performed. Colitis was evaluated based on the disease activity index (DAI) score, colon length, and histological score. Reverse transcription polymerase chain reaction testing, the Western blot assay, and immunohistochemical staining were performed to determine inflammatory cytokine levels. The NI reduced body weight change and the DAI score. Colon length and the histological score were longer and lower in the NI-treated groups, respectively. The NI decreased the expression of pro-inflammatory cytokines, particularly in tumor necrosis factor alpha (TNF-α) and phosphorylated nuclear factor kappa B (p-NF-κB). Immunohistochemical staining revealed decreased inducible nitric oxide synthase (iNOS) and high mobility group box 1 (HMGB1) levels. Overall, the NI improved DSS induced chronic colitis by attenuating the mRNA expression of pro-inflammatory cytokines such as TNF-α. Therefore, NI use is a potential, novel treatment approach for IBD.
不受控制的慢性炎症和坏死是炎症性肠病(IBD)的特征。本研究旨在探讨坏死抑制剂(NI,NecroX-7)对葡聚糖硫酸钠(DSS)诱导的小鼠慢性结肠炎模型的影响。在第1至5天给予DSS,并在第1、3和5天以及在三周周期的前五天每隔一天腹腔注射NI(3mg/kg,30mg/kg)。进行三个周期的给药。基于疾病活动指数(DAI)评分、结肠长度和组织学评分评估结肠炎。进行逆转录聚合酶链反应检测、蛋白质印迹分析和免疫组织化学染色以确定炎性细胞因子水平。NI减轻了体重变化和DAI评分。NI治疗组的结肠长度更长,组织学评分更低。NI降低了促炎细胞因子的表达,特别是肿瘤坏死因子α(TNF-α)和磷酸化核因子κB(p-NF-κB)。免疫组织化学染色显示诱导型一氧化氮合酶(iNOS)和高迁移率族蛋白B1(HMGB1)水平降低。总体而言,NI通过减弱TNF-α等促炎细胞因子的mRNA表达改善了DSS诱导的慢性结肠炎。因此,使用NI是一种潜在的IBD新型治疗方法。