Ullah H M Arif, Saba Evelyn, Lee Yuan Yee, Hong Seung-Bok, Hyun Sun-Hee, Kwak Yi-Seong, Park Chae-Kyu, Kim Sung Dae, Rhee Man Hee
Department of Veterinary Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu, Republic of Korea.
Department of Veterinary Biomedical Sciences, Faculty of Veterinary and Animal Sciences, Pir Mehr Ali Shah-Arid Agriculture University, Pakistan.
J Ginseng Res. 2022 Sep;46(5):628-635. doi: 10.1016/j.jgr.2021.07.001. Epub 2021 Jul 17.
Ulcerative colitis (UC) is the large intestine disease that results in chronic inflammation and ulcers in the colon. Rg3-enriched Korean Red Ginseng extract (Rg3-RGE) is known for its pharmacological activities. (PT) is also used in the treatment of various inflammatory diseases. The aim of this study is to investigate the attenuating effects of Rg3-RGE with PT on oxazolone (OXA)-induced UC in mice.
A total of six groups of mice including control group, OXA (as model group, 1.5%) group, sulfasalazine (75 mg/kg) group, Rg3-RGE (20 mg/kg) group, PT (300 mg/kg) group, and Rg3-RGE (10 mg/kg) with PT (150 mg/kg) group. Data on the colon length, body weight, disease activity index (DAI), histological changes, nitric oxide (NO) assay, Real-time PCR of inflammatory factors, ELISA of inflammatory factors, Western blot, and flow cytometry analysis were obtained.
Overall, the combination treatment of Rg3-RGE and PT significantly improved the colon length and body weight and decreased the DAI in mice compared with the treatment with OXA. Additionally, the histological injury was also reduced by the combination treatment. Moreover, the NO production level and inflammatory mediators and cytokines were significantly downregulated in the Rg3-RGE with the PT group compared with the model group. Also, NLR family pyrin domain containing 3 (NLRP3) inflammasome and nuclear factor kappa B (NF-κB) were suppressed in the combination treatment group compared with the OXA group. Furthermore, the number of immune cell subtypes of CD4 T-helper cells, CD19 B-cells, and CD4 and CD25 regulatory T-cells (Tregs) was improved in the Rg3-RGE with the PT group compared with the OXA group.
Overall, the mixture of Rg3-RGE and PT is an effective therapeutic treatment for UC.
溃疡性结肠炎(UC)是一种导致结肠慢性炎症和溃疡的大肠疾病。富含Rg3的韩国红参提取物(Rg3-RGE)以其药理活性而闻名。柳氮磺胺吡啶(PT)也用于治疗各种炎症性疾病。本研究的目的是探讨Rg3-RGE联合PT对恶唑酮(OXA)诱导的小鼠UC的减轻作用。
共六组小鼠,包括对照组、OXA(作为模型组,1.5%)组、柳氮磺胺吡啶(75 mg/kg)组、Rg3-RGE(20 mg/kg)组、PT(300 mg/kg)组以及Rg3-RGE(10 mg/kg)联合PT(150 mg/kg)组。获取了关于结肠长度、体重、疾病活动指数(DAI)、组织学变化、一氧化氮(NO)检测、炎症因子实时定量聚合酶链反应、炎症因子酶联免疫吸附测定、蛋白质免疫印迹法以及流式细胞术分析的数据。
总体而言,与OXA治疗相比,Rg3-RGE与PT的联合治疗显著改善了小鼠的结肠长度和体重,并降低了DAI。此外,联合治疗还减轻了组织学损伤。而且,与模型组相比,Rg3-RGE联合PT组的NO产生水平以及炎症介质和细胞因子显著下调。同样,与OXA组相比,联合治疗组中含NLR家族吡咯结构域蛋白3(NLRP3)炎性小体和核因子κB(NF-κB)受到抑制。此外,与OXA组相比,Rg3-RGE联合PT组中CD4辅助性T细胞、CD19 B细胞以及CD4和CD25调节性T细胞(Tregs)的免疫细胞亚群数量有所改善。
总体而言,Rg3-RGE与PT的混合物是治疗UC的有效疗法。