溃疡性结肠炎
NF-κB
信号转导
肠道菌群
结肠炎
NFKB1型
生物
医学
免疫学
细胞生物学
转录因子
内科学
生物化学
基因
疾病
作者
Xiaojun Song,Wei Wang,Li Liu,Zitong Zhao,Xuebin Shen,Lingyun Zhou,Yuanxiang Zhang,Daiyin Peng,Sihui Nian
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-05-06
卷期号:29 (9): 2154-2154
被引量:16
标识
DOI:10.3390/molecules29092154
摘要
Ulcerative colitis (UC), as a chronic inflammatory disease, presents a global public health threat. However, the mechanism of Poria cocos (PC) in treating UC remains unclear. Here, LC-MS/MS was carried out to identify the components of PC. The protective effect of PC against UC was evaluated by disease activity index (DAI), colon length and histological analysis in dextran sulfate sodium (DSS)-induced UC mice. ELISA, qPCR, and Western blot tests were conducted to assess the inflammatory state. Western blotting and immunohistochemistry techniques were employed to evaluate the expression of tight junction proteins. The sequencing of 16S rRNA was utilized for the analysis of gut microbiota regulation. The results showed that a total of fifty-two nutrients and active components were identified in PC. After treatment, PC significantly alleviated UC-associated symptoms including body weight loss, shortened colon, an increase in DAI score, histopathologic lesions. PC also reduced the levels of inflammatory cytokines TNF-α, IL-6, and IL-1β, as evidenced by the suppressed NF-κB pathway, restored the tight junction proteins ZO-1 and Claudin-1 in the colon, and promoted the diversity and abundance of beneficial gut microbiota. Collectively, these findings suggest that PC ameliorates colitis symptoms through the reduction in NF-κB signaling activation to mitigate inflammatory damage, thus repairing the intestinal barrier, and regulating the gut microbiota.
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