肠道微生物群-芳香烃受体(AhR)轴介导桑黄菌富含多酚的提取物的抗胆碱作用

IF 23.7 Q1 MICROBIOLOGY
iMeta Pub Date : 2024-03-11 DOI:10.1002/imt2.180
Shi Zhong, Yu-Qing Sun, Jin-Xi Huo, Wen-Yi Xu, Ya-Nan Yang, Jun-Bo Yang, Wei-Jie Wu, Yong-Xin Liu, Chong-Ming Wu, You-Gui Li
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引用次数: 0

摘要

炎症性肠病(IBD)是全球关注的重大健康问题。肠道微生物群在 IBD 的发病和发展中起着至关重要的作用。桑黄菌(Sanghuangporus,SH)是一种传统的中药蘑菇,具有很好的抗炎作用,并能有效调节肠道微生物群。尽管具有这些特性,但三黄菇的具体抗胆固醇作用以及肠道微生物群介导其益处的机制仍不清楚。在这里,我们证明了从 SH 中提取的富含多酚的提取物可通过调节肠道微生物群有效缓解右旋糖酐硫酸钠(DSS)诱导的小鼠结肠炎的病理症状。用 SH 治疗可明显富集阿利司匹斯,尤其是阿利司匹斯 onderdonkii 及其代谢产物 5- 羟基吲哚-3-乙酸(5HIAA)。口服活的A. onderdonkii或5HIAA能有效缓解DSS诱导的小鼠结肠炎。此外,5HIAA和SH都能显著激活芳香烃受体(AhR),而服用AhR拮抗剂则会减弱它们对结肠炎的保护作用。这些结果强调了SH通过促进A. onderdonkii和5HIAA,最终激活AhR信号转导,在减轻DSS诱导的结肠炎方面的强大功效。这项研究揭示了基于 SH 和肠道微生物群之间的相互作用开发结肠炎治疗策略的潜在途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The gut microbiota-aromatic hydrocarbon receptor (AhR) axis mediates the anticolitic effect of polyphenol-rich extracts from Sanghuangporus

The gut microbiota-aromatic hydrocarbon receptor (AhR) axis mediates the anticolitic effect of polyphenol-rich extracts from Sanghuangporus

Inflammatory bowel disease (IBD) is a significant global health concern. The gut microbiota plays an essential role in the onset and development of IBD. Sanghuangporus (SH), a traditional Chinese medicinal mushroom, has excellent anti-inflammatory effects and is effective at modulating the gut microbiota. Despite these attributes, the specific anticolitic effects of SH and the mechanisms through which the gut microbiota mediates its benefits remain unclear. Herein, we demonstrated that polyphenol-rich extract from SH effectively alleviated the pathological symptoms of dextran sodium sulfate (DSS)-induced colitis in mice by modulating the gut microbiota. Treatment with SH distinctly enriched Alistipes, especially Alistipes onderdonkii, and its metabolite 5-hydroxyindole-3-acetic acid (5HIAA). Oral gavage of live A. onderdonkii or 5HIAA potently mitigated DSS-induced colitis in mice. Moreover, both 5HIAA and SH significantly activated the aromatic hydrocarbon receptor (AhR), and the administration of an AhR antagonist abrogated their protective effects against colitis. These results underscore the potent efficacy of SH in diminishing DSS-induced colitis through the promotion of A. onderdonkii and 5HIAA, ultimately activating AhR signaling. This study unveils potential avenues for developing therapeutic strategies for colitis based on the interplay between SH and the gut microbiota.

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