Angelica dahurica Polysaccharides Ameliorate Colitis by Reducing the Restriction of Gut Microbiota-Derived Imidazole Propionate on PPAR-γ Signaling Activation.

IF 6.3 2区 医学 Q1 CHEMISTRY, MEDICINAL
Phytotherapy Research Pub Date : 2025-05-01 Epub Date: 2025-03-05 DOI:10.1002/ptr.8466
Jingyi Hu, Feng Xu, Lei Zhu, Yuan Cui, Ryan Au, Yanan Li, Yiheng Tong, Hong Shen
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引用次数: 0

Abstract

Angelica dahurica radix (ADR), the root of the botanical family Apiaceae (genus Angelica, species Angelica dahurica (Hoffm.)), has been used to treat colitis in clinical practice. The immunomodulatory effects of ADR are attributed to its polysaccharides (RP). However, its mechanism of action has not been elucidated. In this study, RP's structure was determined through nuclear magnetic resonance analysis. Dextran sulfate sodium-induced colitis in mice was utilized to assess the therapeutic efficacy of RP, while experiments involving fecal microbiota transplantation (FMT) and antibiotic treatment were performed to investigate the contribution of gut microbiota to RP's protective function. Non-targeted metabolomics was utilized to identify potential targets for elucidating the underlying mechanisms. RP is likely composed of (→4)-α-D-Glcp-(1→ and →4)-α-D-Galp-(1→). It effectively alleviated DSS-induced colitis by restoring the balance of the gut microbial community, a finding validated through FMT and antibiotic intervention experiments. Imidazole propionate (ImP) emerged as a potential target for RP's efficacy in treating colitis, which inhibits the activation of peroxisome proliferator-activated receptor gamma (PPAR-γ). Our findings suggest that RP may confer protection against colitis by activating the PPAR-γ signaling pathway through alleviating the constraint imposed by ImP.

白芷多糖通过降低肠道微生物源咪唑丙酸对PPAR-γ信号激活的限制改善结肠炎。
白芷(Angelica dahurica radix, ADR)是Apiaceae植物科(当归属,白芷种)的根,在临床上已被用于治疗结肠炎。ADR的免疫调节作用与其多糖(RP)有关。然而,其作用机制尚未阐明。本研究通过核磁共振分析确定RP的结构。采用葡聚糖硫酸钠诱导小鼠结肠炎评价RP的治疗效果,并通过粪便微生物群移植(FMT)和抗生素治疗实验探讨肠道微生物群对RP保护功能的贡献。非靶向代谢组学被用来确定潜在的靶点,以阐明潜在的机制。RP可能由(→4)-α-D-Glcp -(1→→4)α-D-Galp -(1→)。通过FMT和抗生素干预实验证实,它可以通过恢复肠道微生物群落的平衡,有效缓解dss诱导的结肠炎。丙酸咪唑(ImP)抑制过氧化物酶体增殖物激活受体γ (PPAR-γ)的激活,成为RP治疗结肠炎疗效的潜在靶点。我们的研究结果表明,RP可能通过减轻ImP施加的约束,激活PPAR-γ信号通路,从而赋予对结肠炎的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Phytotherapy Research
Phytotherapy Research 医学-药学
CiteScore
12.80
自引率
5.60%
发文量
325
审稿时长
2.6 months
期刊介绍: Phytotherapy Research is an internationally recognized pharmacological journal that serves as a trailblazing resource for biochemists, pharmacologists, and toxicologists. We strive to disseminate groundbreaking research on medicinal plants, pushing the boundaries of knowledge and understanding in this field. Our primary focus areas encompass pharmacology, toxicology, and the clinical applications of herbs and natural products in medicine. We actively encourage submissions on the effects of commonly consumed food ingredients and standardized plant extracts. We welcome a range of contributions including original research papers, review articles, and letters. By providing a platform for the latest developments and discoveries in phytotherapy, we aim to support the advancement of scientific knowledge and contribute to the improvement of modern medicine.
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