Yang Ye Jin, Kim Min Jung, Lee Ho Jeong, Lee Won-Yung, Yang Ju-Hye, Kim Hun Hwan, Shim Min Sup, Heo Ji Woong, Son Jae Dong, Kim Woo H, Kim Gon Sup, Lee Hu-Jang, Kim Young-Woo, Kim Kwang Youn, Park Kwang Il
Departments of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Republic of Korea.
Gyeongnam Bio-Health Research Support Center, Gyeongnam Branch Institute, Korea Institute of Toxicology (KIT), 17 Jeigok-gil, Jinju 52834, Republic of Korea.
Antioxidants (Basel). 2024 May 7;13(5):575. doi: 10.3390/antiox13050575.
Inflammatory bowel disease (IBD) is a chronic inflammatory condition caused by the disruption of the intestinal barrier. The intestinal barrier is maintained by tight junctions (TJs), which sustain intestinal homeostasis and prevent pathogens from entering the microbiome and mucosal tissues. Miller () is a natural substance that has been used in traditional medicine as a therapy for a variety of diseases. However, in IBD, the efficacy of is unknown. Therefore, we evaluated ZJB in Caco2 cells and a dextran sodium sulfate (DSS)-induced mouse model to demonstrate its efficacy in IBD. extracts were prepared using 70% ethanol and were named ZJB. ZJB was found to be non-cytotoxic and to have excellent antioxidant effects. We confirmed its anti-inflammatory properties via the down-regulation of inflammatory factors, including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). To evaluate the effects of ZJB on intestinal barrier function and TJ improvement, the trans-epithelial electrical resistance (TEER) and fluorescein isothiocyanate-dextran 4 kDa (FITC-Dextran 4) permeability were assessed. The TEER value increased by 61.389% and permeability decreased by 27.348% in the 200 μg/mL ZJB group compared with the 50 ng/mL IL-6 group after 24 h. Additionally, ZJB alleviated body weight loss, reduced the disease activity index (DAI) score, and induced colon shortening in 5% DSS-induced mice; inflammatory cytokines, tumor necrosis factor (TNF)-α, and interleukin (IL)-6 were down-regulated in the serum. TJ proteins, such as Zonula occludens (ZO)-1 and occludin, were up-regulated by ZJB in an impaired Caco2 mouse model. Additionally, according to the liquid chromatography results, in tandem with mass spectrometry (LC-MS/MS) analysis, seven active ingredients were detected in ZJB. In conclusion, ZJB down-regulated inflammatory factors, protected intestinal barrier function, and increased TJ proteins. It is thus a safe, natural substance with the potential to be used as a therapeutic agent in IBD treatment.
炎症性肠病(IBD)是一种由肠道屏障破坏引起的慢性炎症性疾病。肠道屏障由紧密连接(TJ)维持,紧密连接维持肠道稳态并防止病原体进入微生物群和黏膜组织。 米勒()是一种天然物质,在传统医学中已被用作多种疾病的治疗方法。然而,在IBD中,其疗效尚不清楚。因此,我们在Caco2细胞和葡聚糖硫酸钠(DSS)诱导的小鼠模型中评估了ZJB,以证明其在IBD中的疗效。 使用70%乙醇制备提取物并将其命名为ZJB。发现ZJB无细胞毒性且具有出色的抗氧化作用。我们通过下调包括诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)在内的炎症因子来证实其抗炎特性。为了评估ZJB对肠道屏障功能和TJ改善的影响,评估了跨上皮电阻(TEER)和异硫氰酸荧光素-葡聚糖4 kDa(FITC-葡聚糖4)通透性。与50 ng/mL IL-6组相比,200 μg/mL ZJB组在24小时后TEER值增加了61.389%,通透性降低了27.348%。此外,ZJB减轻了5% DSS诱导的小鼠体重减轻,降低了疾病活动指数(DAI)评分,并导致结肠缩短;血清中炎症细胞因子、肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6下调。在受损的Caco2小鼠模型中,ZJB上调了紧密连接蛋白,如闭合蛋白(ZO)-1和闭合蛋白。此外,根据液相色谱结果并结合质谱(LC-MS/MS)分析,在ZJB中检测到七种活性成分。总之,ZJB下调炎症因子,保护肠道屏障功能,并增加紧密连接蛋白。因此,它是一种安全的天然物质,有可能用作IBD治疗的治疗剂。