Xiaoyankangjun tablet alleviates dextran sulfate sodium-induced colitis in mice by regulating gut microbiota and JAK2/STAT3 pathway

IF 4.8 3区 化学 Q1 CHEMISTRY, MEDICINAL
Suqin Yang, Jingtao Huang, Wenjing Tan, Xiankun Xia, Dali Gan, Yalei Ren, Hanwen Su, Meixian Xiang
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引用次数: 0

Abstract

Xiaoyankangjun tablet (XYKJP) is a traditional Chinese medicine formulation used to treat intestinal disorders in clinical practice. However, the specific therapeutic mechanism of action of XYKJP in colitis has not yet been elucidated. This study aimed to reveal the multifaceted mechanisms of action of XYKJP in treating colitis. The model established based on DSS-induced colitis in C57BL/6 mice was employed to estimate the effect of XYKJP on colitis, which was then followed by histological assessment, 16S rRNA sequencing, RT-qPCR, ELISA, and Western blot. XYKJP alleviated the symptoms of DSS-induced colitis mainly by reducing oxidative stress, inflammatory responses, and intestinal mucosal repair in colitis tissues. In addition, XYKJP regulated the intestinal flora by increasing the relative abundance of Akkermansia and Bifidobacterium and reducing the relative abundance of Coriobacteriaceae_UCG-002. Mechanistically, XYKJP increased the content of short-chain fatty acids (SCFAs) in the feces, particularly propanoic acid and butyric acid, activated their specific receptor GPR43/41, furthermore activated the Nrf2/HO-1 pathway, and suppressed the JAK2/STAT3 pathway. XYKJP significantly alleviated the symptoms of experimental colitis and functioned synergistically by regulating the intestinal flora, increasing the production of SCFAs, and activating their specific receptors, thereby repressing oxidative stress and inflammation.

Graphical Abstract

Abstract Image

小安康君片通过调节肠道微生物群和JAK2/STAT3通路缓解右旋糖酐硫酸钠诱导的小鼠结肠炎
小阳康君片(XYKJP)是一种传统中药配方,临床上用于治疗肠道疾病。然而,XYKJP 对结肠炎的具体治疗作用机制尚未阐明。本研究旨在揭示 XYKJP 治疗结肠炎的多重作用机制。本研究以 DSS 诱导的 C57BL/6 小鼠结肠炎为模型,通过组织学评估、16S rRNA 测序、RT-qPCR、ELISA 和 Western blot 等方法评估 XYKJP 对结肠炎的影响。XYKJP主要通过减少氧化应激、炎症反应和结肠炎组织的肠粘膜修复来缓解DSS诱导的结肠炎症状。此外,XYKJP 还通过增加 Akkermansia 和 Bifidobacterium 的相对丰度以及降低 Coriobacteriaceae_UCG-002 的相对丰度来调节肠道菌群。从机理上讲,XYKJP 增加了粪便中短链脂肪酸(SCFAs)的含量,尤其是丙酸和丁酸,激活了它们的特异性受体 GPR43/41,进一步激活了 Nrf2/HO-1 通路,抑制了 JAK2/STAT3 通路。XYKJP 能明显缓解实验性结肠炎的症状,并通过调节肠道菌群、增加 SCFAs 的产生和激活其特异性受体发挥协同作用,从而抑制氧化应激和炎症。
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来源期刊
Natural Products and Bioprospecting
Natural Products and Bioprospecting CHEMISTRY, MEDICINAL-
CiteScore
8.30
自引率
2.10%
发文量
39
审稿时长
13 weeks
期刊介绍: Natural Products and Bioprospecting serves as an international forum for essential research on natural products and focuses on, but is not limited to, the following aspects: Natural products: isolation and structure elucidation Natural products: synthesis Biological evaluation of biologically active natural products Bioorganic and medicinal chemistry Biosynthesis and microbiological transformation Fermentation and plant tissue cultures Bioprospecting of natural products from natural resources All research articles published in this journal have undergone rigorous peer review. In addition to original research articles, Natural Products and Bioprospecting publishes reviews and short communications, aiming to rapidly disseminate the research results of timely interest, and comprehensive reviews of emerging topics in all the areas of natural products. It is also an open access journal, which provides free access to its articles to anyone, anywhere.
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