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胆汁酸通过法尼醇X受体(FXR)和G蛋白偶联胆汁酸受体5(TGR5)影响肠道屏障功能。

Bile acids affect intestinal barrier function through FXR and TGR5.

作者信息

Song Guangyao, Xie Yuxiao, Yi Lanlan, Cheng Wenjie, Jia Huijin, Shi Wenzhe, Liu Qiwei, Fang Ligui, Xue Shiqi, Liu Dan, Zhu Junhong, Zhao Sumei

机构信息

College of Animal Science and Technology, Yunnan Agricultural University, Kunming, China.

College of Biology and Agriculture, Zunyi Normal University, Zunyi, China.

出版信息

Front Med (Lausanne). 2025 Jul 7;12:1607899. doi: 10.3389/fmed.2025.1607899. eCollection 2025.

DOI:10.3389/fmed.2025.1607899
PMID:40692955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12277261/
Abstract

Bile acids play a dual role by aiding lipid absorption and acting as signaling molecules by interacting with various receptors. Bile acids are perpetually recycled via enterohepatic circulation and are biotransformation by gut microbiota, making bile acid metabolism a critical regulator of intestinal homeostasis. The intestinal epithelium prominently expresses two key bile acid receptors - the farnesoid X receptor (FXR) and G protein-coupled bile acid receptor 1 (TGR5) - which play indispensable roles in maintaining bile acid homeostasis and intestinal barrier function. Due to the abundant expression of bile acid receptors and the importance of the intestine in preventing pathogen invasion, researchers are increasingly focused on the function of bile acids in this system. This article focuses on the effect of bile acids and their receptors, FXR and the TGR5, in modulating intestinal barrier function.

摘要

胆汁酸通过辅助脂质吸收以及与各种受体相互作用充当信号分子,发挥双重作用。胆汁酸通过肠肝循环不断循环,并由肠道微生物群进行生物转化,使得胆汁酸代谢成为肠道内环境稳态的关键调节因子。肠上皮细胞显著表达两种关键的胆汁酸受体——法尼醇X受体(FXR)和G蛋白偶联胆汁酸受体1(TGR5),它们在维持胆汁酸稳态和肠道屏障功能中发挥着不可或缺的作用。由于胆汁酸受体的大量表达以及肠道在预防病原体入侵中的重要性,研究人员越来越关注胆汁酸在该系统中的功能。本文重点探讨胆汁酸及其受体FXR和TGR5在调节肠道屏障功能方面的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/5420e491420f/fmed-12-1607899-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/74acce9011f7/fmed-12-1607899-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/079c883db632/fmed-12-1607899-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/5420e491420f/fmed-12-1607899-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/74acce9011f7/fmed-12-1607899-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/079c883db632/fmed-12-1607899-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7f/12277261/5420e491420f/fmed-12-1607899-g003.jpg

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本文引用的文献

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2
FXR deletion attenuates intestinal barrier dysfunction in murine acute intestinal inflammation.FXR 缺失可减轻急性肠道炎症小鼠的肠道屏障功能障碍。
Am J Physiol Gastrointest Liver Physiol. 2024 Aug 1;327(2):G175-G187. doi: 10.1152/ajpgi.00063.2024. Epub 2024 Jun 11.
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Bile Acids, Intestinal Barrier Dysfunction, and Related Diseases.
胆汁酸、肠道屏障功能障碍与相关疾病
Cells. 2023 Jul 19;12(14):1888. doi: 10.3390/cells12141888.
4
Role of mucosal immunity and epithelial-vascular barrier in modulating gut homeostasis.黏膜免疫和上皮血管屏障在调节肠道稳态中的作用。
Intern Emerg Med. 2023 Sep;18(6):1635-1646. doi: 10.1007/s11739-023-03329-1. Epub 2023 Jul 4.
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The Mucin Family of Proteins: Candidates as Potential Biomarkers for Colon Cancer.粘蛋白家族蛋白:作为结肠癌潜在生物标志物的候选物
Cancers (Basel). 2023 Feb 27;15(5):1491. doi: 10.3390/cancers15051491.
6
Autophagy controls mucus secretion from intestinal goblet cells by alleviating ER stress.自噬通过缓解内质网应激控制肠道杯状细胞的黏液分泌。
Cell Host Microbe. 2023 Mar 8;31(3):433-446.e4. doi: 10.1016/j.chom.2023.01.006. Epub 2023 Feb 3.
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Gut microbiota-derived ursodeoxycholic acid alleviates low birth weight-induced colonic inflammation by enhancing M2 macrophage polarization.肠道微生物衍生的熊去氧胆酸通过增强 M2 巨噬细胞极化缓解低出生体重引起的结肠炎症。
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