Yang Ye Jin, Kim Min Jung, Heo Ji Woong, Kim Hun Hwan, Kim Gon Sup, Shim Min Sub, Kim Kwang Youn, Park Kwang Il
College of Veterinary Medicine, Gyeongsang National University, 501 Jinjudaero, Gazwa, Jinju 52828, Republic of Korea.
Department of Biochemistry and Molecular Genetics, College of Graduate Studies, Midwestern University, 19555 N. 59th Ave., Glendale, AZ 85308, USA.
Antioxidants (Basel). 2025 Mar 20;14(3):370. doi: 10.3390/antiox14030370.
Korean mistletoe ( var. , KML) offers remarkable therapeutic potential for a variety of diseases. This study aims to evaluate the effects and potential molecular mechanisms of KML ethanol extracts (KMLE), focusing on intestinal barrier function and tight junctions (TJs) in an interleukin (IL)-6-induced Caco-2 cell monolayer model and a dextran sodium sulfate (DSS)-induced ulcerative colitis (UC) mouse model. KMLE is non-cytotoxic in Caco-2 cells and demonstrated strong antioxidant activity. KMLE alleviated significant barrier dysfunction and protected tight junction proteins (TJPs) in vitro. Furthermore, KMLE alleviated clinical symptoms and histopathological damage, upregulated TJPs, and suppressed the inflammatory cytokines in vivo. Additionally, six bioactive compounds were identified in KMLE by liquid chromatography-tandem mass spectrometry (LC-MS/MS). In conclusion, KMLE ameliorated intestinal barrier dysfunction in vitro and in vivo. These findings underscore the potential of KMLE as a therapeutic agent for UC, providing insights into the mechanisms through anti-inflammatory properties and its ability to restore TJ integrity.
韩国槲寄生(变种,KML)对多种疾病具有显著的治疗潜力。本研究旨在评估KML乙醇提取物(KMLE)的作用及潜在分子机制,重点关注白细胞介素(IL)-6诱导的Caco-2细胞单层模型和葡聚糖硫酸钠(DSS)诱导的溃疡性结肠炎(UC)小鼠模型中的肠道屏障功能和紧密连接(TJ)。KMLE对Caco-2细胞无细胞毒性,并表现出强大的抗氧化活性。KMLE在体外减轻了显著的屏障功能障碍并保护了紧密连接蛋白(TJP)。此外,KMLE在体内减轻了临床症状和组织病理学损伤,上调了TJP,并抑制了炎性细胞因子。另外,通过液相色谱-串联质谱(LC-MS/MS)在KMLE中鉴定出六种生物活性化合物。总之,KMLE在体外和体内均改善了肠道屏障功能障碍。这些发现强调了KMLE作为UC治疗剂的潜力,通过抗炎特性及其恢复TJ完整性的能力为作用机制提供了见解。