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肠易激综合征中胆汁酸与肠道微生物群的相互作用

Bile acid-gut microbiota crosstalk in irritable bowel syndrome.

作者信息

Gu Yu, Li Lingfeng, Yang Min, Liu Tianyu, Song Xueli, Qin Xiali, Xu Xin, Liu Jinghua, Wang Bangmao, Cao Hailong

机构信息

Department of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, Tianjin, China.

Department of Gastroenterology, Tianjin TEDA hospital, Tianjin, China.

出版信息

Crit Rev Microbiol. 2023 May;49(3):350-369. doi: 10.1080/1040841X.2022.2058353. Epub 2022 Apr 7.


DOI:10.1080/1040841X.2022.2058353
PMID:35389754
Abstract

Irritable bowel syndrome (IBS) is a common disorder of gut-brain interaction with an increasing prevalence, and its precise aetiology remains unclear. Gut microbiota dysbiosis has been found to be associated with IBS pathogenesis. In addition, a high incidence of bile acid diarrhoea and disturbed bile acid metabolism has been observed in IBS patients. The abundant microorganisms inhabited in human gut have essential functions in bile acid biotransformation, and can immensely affect the size and constitution of bile acid pool. Meanwhile, the alterations of bile acid profile can inversely interfere with the gut microbiota. This review discussed the role of intricate correlations between bile acids and gut microbiota in IBS pathogenesis and delineated the possible molecular mechanisms, mainly the signalling induced by farnesoid X receptor and transmembrane G protein-coupled receptor 5. Besides, some biomarkers for identifying bile acid diarrhoea in IBS population were listed, assisting the diagnosis and classification of IBS. Moreover, it also assessed some therapeutic strategies for IBS that regulate the bile acid-gut microbiota axis, such as dietary modulation, probiotics/prebiotics, faecal microbiota transplantation, and antibiotics. Collectively, this article illustrated the relationship between bile acids and gut microbiota in IBS pathophysiology and might offer some novel therapeutic options for IBS.

摘要

肠易激综合征(IBS)是一种常见的肠-脑互动障碍性疾病,患病率呈上升趋势,其确切病因尚不清楚。肠道微生物群失调已被发现与IBS的发病机制有关。此外,在IBS患者中观察到胆汁酸腹泻的高发病率和胆汁酸代谢紊乱。栖息在人体肠道中的丰富微生物在胆汁酸生物转化中具有重要作用,并可极大地影响胆汁酸池的大小和组成。同时,胆汁酸谱的改变可反过来干扰肠道微生物群。本综述讨论了胆汁酸与肠道微生物群之间复杂的相关性在IBS发病机制中的作用,并阐述了可能的分子机制,主要是法尼醇X受体和跨膜G蛋白偶联受体5诱导的信号传导。此外,还列出了一些用于识别IBS人群中胆汁酸腹泻的生物标志物,有助于IBS的诊断和分类。此外,还评估了一些调节胆汁酸-肠道微生物群轴的IBS治疗策略,如饮食调节、益生菌/益生元、粪便微生物群移植和抗生素。总的来说,本文阐述了胆汁酸与肠道微生物群在IBS病理生理学中的关系,并可能为IBS提供一些新的治疗选择。

相似文献

[1]
Bile acid-gut microbiota crosstalk in irritable bowel syndrome.

Crit Rev Microbiol. 2023-5

[2]
Gut Microbiota-Bile Acid Crosstalk in Diarrhea-Irritable Bowel Syndrome.

Biomed Res Int. 2020

[3]
Intestinal crosstalk between bile acids and microbiota in irritable bowel syndrome.

J Gastroenterol Hepatol. 2023-7

[4]
The function of the gut microbiota-bile acid-TGR5 axis in diarrhea-predominant irritable bowel syndrome.

mSystems. 2024-3-19

[5]
Altered metabolism of bile acids correlates with clinical parameters and the gut microbiota in patients with diarrhea-predominant irritable bowel syndrome.

World J Gastroenterol. 2020-12-7

[6]
Interplay between gut microbiota and bile acids in diarrhoea-predominant irritable bowel syndrome: a review.

Crit Rev Microbiol. 2022-11

[7]
Tong-Xie-Yao-Fang strengthens intestinal feedback control of bile acid synthesis to ameliorate irritable bowel syndrome by enhancing bile salt hydrolase-expressing microbiota.

J Ethnopharmacol. 2024-9-15

[8]
Gut Microbiota-Derived Metabolites in Irritable Bowel Syndrome.

Front Cell Infect Microbiol. 2021

[9]
Targeting the gut microbiota for the treatment of irritable bowel syndrome.

Kaohsiung J Med Sci. 2019-11-29

[10]
Modulation of the gut microbiota: a focus on treatments for irritable bowel syndrome.

Postgrad Med. 2017-11

引用本文的文献

[1]
Therapeutic Potential of Flavonoids and Flavonoid-Rich Compounds in Irritable Bowel Syndrome.

Drug Des Devel Ther. 2025-6-6

[2]
The alteration of mucosal bile acid profile is associated with nerve growth factor expression in mast cells and bowel symptoms in diarrhea-predominant irritable bowel syndrome.

Clin Exp Immunol. 2024-4-23

[3]
Effects of Different Types of Dietary Fibers on Lipid Metabolism and Bile Acids in Weaned Piglets.

Animals (Basel). 2023-10-19

[4]
Regulation of gut microbiota-bile acids axis by probiotics in inflammatory bowel disease.

Front Immunol. 2022

[5]
The gut microbiota-bile acid axis: A potential therapeutic target for liver fibrosis.

Front Cell Infect Microbiol. 2022

[6]
Mucin O-glycan-microbiota axis orchestrates gut homeostasis in a diarrheal pig model.

Microbiome. 2022-8-31

[7]
Metabolomics: The Key to Unraveling the Role of the Microbiome in Visceral Pain Neurotransmission.

Front Neurosci. 2022-6-23

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