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多组学揭示了黄连素通过调节肠道微生物群和肠-肝轴中的胆汁酸代谢对溃疡性结肠炎的缓解作用。

Multi-omics reveals the alleviating effect of berberine on ulcerative colitis through modulating the gut microbiome and bile acid metabolism in the gut-liver axis.

作者信息

Yu Jingsheng, Zheng Yixuan, Liu Changmin, Xie Zhuangyuan, Liu Qingqing, Yang Shuai, Tian Qianqian, Song Chi, Chen Shilin

机构信息

Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.

Institute of Herbgenomics, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Pharmacol. 2024 Oct 24;15:1494210. doi: 10.3389/fphar.2024.1494210. eCollection 2024.


DOI:10.3389/fphar.2024.1494210
PMID:39512826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11540792/
Abstract

The dysfunction of gut microbiome and bile acid metabolism might cause the incidence and relapse of ulcerative colitis (UC). Thus, natural products have been considered effective for UC through the regulation of gut microbiome and bile acid. In this study, we evaluated the regulatory effect of berberine on gut microbiome and bile acid metabolism in UC. Results showed that the relative abundances of beneficial bacteria showed a decreasing trend in the UC model, and the taurine conjugated bile acids increased from the liver tissue to the colon tissue. Berberine inhibited the colonization of harmful bacteria and promoted the primary bile acid metabolism. Moreover, we used multi-omics technology (metagenomics, metabolomics, and transcriptomics technology) to reveal that berberine restored the intestinal barrier function through bile acid/S1PR2/RhoA/ROCK pathway. The result of transmission electron microscopy directly showed that the damaged intestinal mucosal barrier was repaired through the berberine treatment. This study revealed the treatment influence on UC through multi-omics technology and models, which provides references for explaining the mechanism of berberine on UC.

摘要

肠道微生物群和胆汁酸代谢功能障碍可能导致溃疡性结肠炎(UC)的发生和复发。因此,天然产物被认为可通过调节肠道微生物群和胆汁酸对UC有效。在本研究中,我们评估了小檗碱对UC中肠道微生物群和胆汁酸代谢的调节作用。结果显示,有益菌的相对丰度在UC模型中呈下降趋势,且牛磺酸结合型胆汁酸从肝脏组织到结肠组织增加。小檗碱抑制有害菌的定植并促进初级胆汁酸代谢。此外,我们使用多组学技术(宏基因组学、代谢组学和转录组学技术)揭示小檗碱通过胆汁酸/S1PR2/RhoA/ROCK途径恢复肠道屏障功能。透射电子显微镜结果直接显示,经小檗碱处理后受损的肠黏膜屏障得以修复。本研究通过多组学技术和模型揭示了对UC的治疗影响,为解释小檗碱对UC的作用机制提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/3619018e3155/fphar-15-1494210-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/0e67b916a999/fphar-15-1494210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/9806f6d584ad/fphar-15-1494210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/322073a4d821/fphar-15-1494210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/669a2fb8efe8/fphar-15-1494210-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/fb677ded0702/fphar-15-1494210-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/98c3cd4f3a22/fphar-15-1494210-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/3619018e3155/fphar-15-1494210-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/0e67b916a999/fphar-15-1494210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/9806f6d584ad/fphar-15-1494210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/322073a4d821/fphar-15-1494210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/669a2fb8efe8/fphar-15-1494210-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/fb677ded0702/fphar-15-1494210-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/98c3cd4f3a22/fphar-15-1494210-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4d1/11540792/3619018e3155/fphar-15-1494210-g007.jpg

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引用本文的文献

[1]
Berberine as a Bioactive Alkaloid: Multi-Omics Perspectives on Its Role in Obesity Management.

Metabolites. 2025-7-9

[2]
Targeting Bile-Acid Metabolism: Nutritional and Microbial Approaches to Alleviate Ulcerative Colitis.

Nutrients. 2025-3-28

[3]
Patchoulene epoxide mitigates colitis and hepatic damage induced by dextran sulfate sodium by regulating the colonic microbiota and purine metabolism.

Front Immunol. 2025-2-14

本文引用的文献

[1]
Anti-diabetic effect of dicaffeoylquinic acids is associated with the modulation of gut microbiota and bile acid metabolism.

J Adv Res. 2025-6

[2]
Taurine-conjugated bile acids and their link to hepatic S1PR2 play a significant role in hepatitis C-related liver disease.

Hepatol Commun. 2024-7-1

[3]
Microbiome-metabolomics-based insight into the protective effects of dietary fiber from sweetpotato residues on the high-fat diet-induced intestinal integrity damage.

Int J Biol Macromol. 2024-8

[4]
Inhibiting the CB1 receptor in CIH-induced animal model alleviates colon injury.

Appl Microbiol Biotechnol. 2024-6-18

[5]
Protective effects of tauroursodeoxycholate against radiation-induced intestinal injury in a mouse model.

Biochem Biophys Res Commun. 2024-9-10

[6]
Study on the mechanism of modified Gegen Qinlian decoction in regulating the intestinal flora-bile acid-TGR5 axis for the treatment of type 2 diabetes mellitus based on macro genome sequencing and targeted metabonomics integration.

Phytomedicine. 2024-9

[7]
Butylparaben induces glycolipid metabolic disorders in mice via disruption of gut microbiota and FXR signaling.

J Hazard Mater. 2024-8-5

[8]
Inhalable metal-organic framework-mediated cuproptosis combined with PD-L1 checkpoint blockade for lung metastasis synergistic immunotherapy.

Acta Pharm Sin B. 2024-5

[9]
Serum bile acid and unsaturated fatty acid profiles of non-alcoholic fatty liver disease in type 2 diabetic patients.

World J Diabetes. 2024-5-15

[10]
Preservation of conjugated primary bile acids by oxygenation of the small intestinal microbiota .

mBio. 2024-6-12

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