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整合多组学揭示了科莱特和赫姆斯尔多糖在小鼠葡聚糖硫酸钠(DSS)模型中的抗结肠炎机制。

Integrative Multi-Omics Reveals the Anti-Colitis Mechanisms of Collett & Hemsl Polysaccharides in a Mouse DSS Model.

作者信息

Li Siyu, Xu Xingrui, Pan Yuezhi, Chen Yu, Wu Zihuan, Cai Shengbao

机构信息

Faculty of Food Science and Engineering, Kunming University of Science and Technology, Kunming 650500, China.

Yunnan Specialty Food Biosynthesis and Biomanufacturing Group, Kunming University of Science and Technology, Kunming 650500, China.

出版信息

Nutrients. 2025 Sep 8;17(17):2895. doi: 10.3390/nu17172895.

Abstract

: Ulcerative colitis (UC) incidence has risen alarmingly worldwide, posing significant clinical challenges due to limitations of therapeutic efficacy and side effects of current drugs. While polysaccharides (PKPs) exhibit anti-inflammatory and antioxidant properties, their anti-colitis potential remains unexplored. This study aimed to validate the protective effects of PKPs against dextran sulfate sodium (DSS)-induced colitis and elucidate its mechanisms. : Acute UC was induced in C57BL/6J mice by 3% DSS. PKPs (125 mg/kg) were administered via gavage for 10 days. Integrated approaches included histopathology, tight junction protein (ZO-1/Occludin/Claudin-1) immunohistochemistry, inflammatory/oxidative markers (ELISA), Nrf2 pathway proteins (Western blot), 16S rRNA gut microbiota sequencing, fecal untargeted metabolomics (UHPLC-MS), short-chain fatty acids (SCFAs) analysis and combined analysis. : PKPs significantly alleviated colitis phenotypes: reduced weight loss, lowered disease activity index (DAI), and attenuated colon shortening. They restored intestinal barrier integrity by upregulating tight junction proteins and reducing plasma Diamine Oxidase (DAO)/D-lactate (D-Lac)/Endotoxin (ET). PKPs suppressed pro-inflammatory cytokines (TNF-α/IL-1β/IL-6) while elevating IL-10, activated the Nrf2/HO-1/NQO1 antioxidant pathway, and reduced oxidative stress (MDA decreased, SOD/GSH increased). Multi-omics revealed PKPs enriched beneficial bacteria (, , ), restored SCFAs (acetate/propionate/butyrate), and modulated metabolic pathways (sphingolipid/linoleic acid metabolism). : PKPs ameliorate DSS-induced colitis through multi-target mechanisms: (1) preserving intestinal barrier function, (2) suppressing inflammation and oxidative stress via Nrf2 activation, (3) restoring gut microbiota balance and SCFA production, and (4) regulating host-microbiota metabolic interactions. These findings support PKPs as a promising dietary supplement for UC management.

摘要

溃疡性结肠炎(UC)在全球范围内的发病率惊人地上升,由于当前药物治疗效果的局限性和副作用,带来了重大的临床挑战。虽然多糖(PKPs)具有抗炎和抗氧化特性,但其抗结肠炎的潜力尚未得到探索。本研究旨在验证PKPs对葡聚糖硫酸钠(DSS)诱导的结肠炎的保护作用,并阐明其机制。:通过3% DSS诱导C57BL/6J小鼠发生急性UC。通过灌胃给予PKPs(125 mg/kg),持续10天。综合方法包括组织病理学、紧密连接蛋白(ZO-1/闭合蛋白/ Claudin-1)免疫组织化学、炎症/氧化标志物(ELISA)、Nrf2通路蛋白(蛋白质印迹法)、16S rRNA肠道微生物群测序、粪便非靶向代谢组学(超高效液相色谱-质谱联用)、短链脂肪酸(SCFAs)分析以及联合分析。:PKPs显著减轻了结肠炎表型:减轻体重减轻、降低疾病活动指数(DAI)并减轻结肠缩短。它们通过上调紧密连接蛋白和降低血浆二胺氧化酶(DAO)/ D-乳酸(D-Lac)/内毒素(ET)来恢复肠道屏障完整性。PKPs抑制促炎细胞因子(TNF-α/IL-1β/IL-6),同时升高IL-10,激活Nrf2/HO-1/NQO1抗氧化途径,并降低氧化应激(丙二醛减少,超氧化物歧化酶/谷胱甘肽增加)。多组学研究表明,PKPs使有益细菌(、、)富集,恢复SCFAs(乙酸盐/丙酸盐/丁酸盐),并调节代谢途径(鞘脂/亚油酸代谢)。:PKPs通过多靶点机制改善DSS诱导的结肠炎:(1)维持肠道屏障功能,(2)通过激活Nrf2抑制炎症和氧化应激,(3)恢复肠道微生物群平衡和SCFA产生,以及(4)调节宿主-微生物群代谢相互作用。这些发现支持PKPs作为一种有前景的用于UC管理的膳食补充剂。

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