灵芝多糖对葡聚糖硫酸钠诱导小鼠溃疡性结肠炎的治疗作用研究

Study on the Therapeutic Effect of Ganoderma lucidum Polysaccharide on Dextran Sulfate Sodium Induced Ulcerative Colitis in Mice

本研究旨在探讨灵芝多糖(GLP)对溃疡性结肠炎(UC)的干预效果。通过建立葡聚糖硫酸钠(DSS)诱导的小鼠UC模型, 将实验动物随机分为正常对照组(Ctrl)、DSS模型组(DSS)以及GLP处理组, 并系统评估各组小鼠的体重变化、疾病活动指数(DAI)、结肠长度、组织病理学特征及炎症因子表达水平, 以综合评价GLP的治疗潜力。结果显示: 与DSS组相比, GLP干预可显著缓解小鼠体重下降、结肠缩短, 降低DAI评分; HE染色表明GLP改善结肠黏膜损伤并减少炎症细胞浸润; qPCR显示GLP下调结肠黏膜中促炎因子Il-6和Tnf-α的mRNA表达。综上, GLP可通过抑制肠道炎症, 改善DSS诱导的小鼠UC症状及病理损伤, 为其后续研究与应用提供实验依据。

This study aims to investigate the interventional effects of Ganoderma lucidum polysaccharide (GLP) on ulcerative colitis (UC) . A mouse model of UC was established by induction with dextran sulfate sodium (DSS) . The experimental animals were randomly divided into a normal control group (Ctrl) , a DSS model group (DSS) , and a GLP treatment group. A systematic evaluation was conducted to assess changes in body weight, disease activity index (DAI) , colon length, histopathological features, and inflammatory cytokine expression levels in mice from each group to comprehensively evaluate the therapeutic potential of GLP. The results showed that, compared to the DSS group, GLP intervention significantly alleviated body weight loss, colon shortening, and decreased the DAI score. H&E staining indicated that GLP improved colonic mucosal damage and reduced inflammatory cell infiltration. qPCR results demonstrated that GLP down regulated the mRNA expression of the pro-inflammatory factors Il-6 and Tnf-α in the colonic mucosa. In conclusion, GLP can alleviate DSS-induced UC symptoms and pathological damage in mice by suppressing intestinal inflammation, providing an experimental basis for its further research and application.