溃疡性结肠炎
淋巴系统
脾脏
免疫系统
免疫
结肠炎
促炎细胞因子
肠系膜淋巴结
医学
淋巴管内皮
炎症
免疫学
药理学
内科学
疾病
作者
Yang Liu,Yahui Dong,Wei Shen,Jiahui DU,Quanwei Sun,Ye Yang,Dengke Yin
标识
DOI:10.1016/s1875-5364(23)60435-2
摘要
Platycodon grandiflorus polysaccharide (PGP) is one of the main components of P. grandiflorus, but the mechanism of its anti-inflammatory effect has not been fully elucidated. The aim of this study was to evaluate the therapeutic effect of PGP on mice with dextran sodium sulfate (DSS)-induced ulcerative colitis (UC) and explore the underlying mechanisms. The results showed that PGP treatment inhibited the weight loss of DSS-induced UC mice, increased colon length, and reduced DAI, spleen index, and pathological damage within the colon. PGP also reduced the levels of pro-inflammatory cytokines and inhibited the enhancement of oxidative stress and MPO activity. Meanwhile, PGP restored the levels of Th1, Th2, Th17, and Treg cell-related cytokines and transcription factors in the colon to regulate colonic immunity. Further studies revealed that PGP regulated the balance of colonic immune cells through mesenteric lymphatic circulation. Taken together, PGP exerts anti-inflammatory and anti-oxidant effect and regulates colonic immunity to attenuate DSS-induced UC through mesenteric lymphatic circulation.
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