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榆耳多糖对DSS诱导小鼠溃疡性结肠炎的改善作用OA

Ameliorative Effects of Gloeostereum incarnatum Polysaccharides on Dextran Sulfate Sodium-Induced Ulcerative Colitis in Mice

中文摘要英文摘要

为探究榆耳(Gloeostereum incarnatum)多糖(GIP)对 3%葡聚糖硫酸钠(dextran sulfate sodium salt,DSS)诱导小鼠溃疡性结肠炎的改善作用,将小鼠随机分为空白组(CON)、模型组(DSS)、榆耳多糖组(低、中、高剂量分别为50、100、200 mg·kg-1,命名为GIPL、GIPM、GIPH)、阳性组(200mg·kg-1柳氮磺吡啶,salazosulfapyridine,SASP).采用酶联免疫吸附实验(enzyme-linked immunosorbent assay,ELISA)测定肿瘤坏死因子TNF-α和白细胞介素IL-6炎症因子及丙二醛(MDA)含量,二胺氧化酶(diamine oxidase,DAO)、乳酸脱氢酶(LDH)、还原型谷胱甘肽酶(GSH)、超氧化物歧化酶(SOD)活性;采用Western Blot检测NF-κB信号通路相关蛋白及肠道紧密连接相关蛋白ZO-1和Occludin的表达量.结果表明:与DSS相比,GIPM、GIPH小鼠结肠受损程度得到显著改善,GIPH的体质量明显回升,GIPM、GIPH小鼠疾病活动指数(disease activity index,DAI)及DAO活性明显减轻,修复结肠组织病理结构,改善黏膜坏死、炎性细胞浸润状态,恢复组织正常形态;GIPM、GIPH可显著提升GSH活性,GIPL、GIPM、GIPH可显著提升SOD活性,降低MDA含量,LDH活性;同时GIPL、GIPM、GIPH可显著下调血清中IL-6、TNF-α促炎因子含量;GIPM、GIPH可上调肠道紧密连接蛋白ZO-1,Occludin的表达,能抑制NF-κB炎症信号通路的激活,研究结果可为榆耳在防治溃疡性结肠炎的开发应用提供参考.

To investigate the ameliorative effects of Gloeostereum incarnatum polysaccharides(GIP)on ulcerative colitis induced by 3%dextran sulfate sodium salt(DSS)in mice,animals were randomly assigned into the following groups:blank control(CON),DSS model(DSS),low-dose GIP(GIPL,50 mg·kg-1),medium-dose GIP(GIPM,100 mg·kg-1),high-dose GIP(GIPH,200 mg·kg-1),and a positive control group treated with salazosulfapyridine(SASP,200 mg·kg-1).Enzyme-linked immunosorbent assay(ELISA)was used to determine serum levels of pro-inflammatory cytokines(TNF-α,IL-6),content of the oxidative stress marker malondialdehyde(MDA),and the activities of diamine oxidase(DAO),lactate dehydrogenase(LDH),reduced glutathione(GSH),and superoxide dismutase(SOD).Western blot analysis was conducted to detect the expression of proteins related to the NF-κB signaling pathway and the intestinal tight junction-related proteins ZO-1 and Occludin.The results showed that compared with the DSS model group,GIPM and GIPH significantly ameliorated colonic tissue damage,with body weight notably restored in the GIPH group.Both GIPM and GIPH groups exhibited significantly reduced disease activity index(DAI)scores and DAO activity.Histopathological examination revealed that GIPM and GIPH treatment repaired colonic tissue architecture,ameliorated mucosal necrosis and inflammatory cell infiltration,and restored normal tissue morphology.GIPM and GIPH also significantly increased GSH activity,and all GIP dose groups(GIPL,GIPM,GIPH)significantly increased SOD activity while decreasing MDA content and LDH activity.Serum levels of the pro-inflammatory cytokines IL-6 and TNF-α were also significantly decreased across all GIP groups.GIPM and GIPH upregulated the expression of the intestinal tight junction proteins ZO-1 and Occludin,and suppressed the activation of the NF-κB inflammatory signaling pathway.These findings suggest that GIP effectively alleviates DSS-induced UC by modulating oxidative stress,suppressing inflammation,and restoring intestinal barrier integrity through the NF-κB signaling pathway,providing a reference for the development of G.incarnatum as a functional food or therapeutic agent for ulcerative colitis.

王伊雯;王雪;王荏瑛;夏梦茁;宋明杰;包海鹰

吉林农业大学中药材学院,吉林长春 130118吉林农业大学中药材学院,吉林长春 130118吉林农业大学中药材学院,吉林长春 130118吉林农业大学中药材学院,吉林长春 130118吉林农业大学中药材学院,吉林长春 130118吉林农业大学中药材学院,吉林长春 130118

榆耳氧化应激NF-κB炎症因子紧密连接蛋白

Gloeostereum incarnatumoxidative stressNF-κBinflammatory cytokinestight junction proteins

《食用菌学报》 2026 (4)

82-92,11

吉林省科技发展计划农业关键技术研发专项(20240303058NC)

10.16488/j.cnki.1005-9873.2026.04.009

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