• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肠道微生物群在疾病中对胆汁酸代谢相关信号通路的调控。

Regulation of bile acid metabolism-related signaling pathways by gut microbiota in diseases.

机构信息

State Key Laboratory of Bioelectronics, School of Biological Science & Medical Engineering, Southeast University, Nanjing 210096, China.

School of Medicine, Southeast University, Nanjing 210097, China.

出版信息

J Zhejiang Univ Sci B. 2019;20(10):781-792. doi: 10.1631/jzus.B1900073.

DOI:10.1631/jzus.B1900073
PMID:31489798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6751489/
Abstract

Over the past decade, there has been increasing attention on the interaction between microbiota and bile acid metabolism. Bile acids are not only involved in the metabolism of nutrients, but are also important in signal transduction for the regulation of host physiological activities. Microbial-regulated bile acid metabolism has been proven to affect many diseases, but there have not been many studies of disease regulation by microbial receptor signaling pathways. This review considers findings of recent research on the core roles of farnesoid X receptor (FXR), G protein-coupled bile acid receptor (TGR5), and vitamin D receptor (VDR) signaling pathways in microbial-host interactions in health and disease. Studying the relationship between these pathways can help us understand the pathogenesis of human diseases, and lead to new solutions for their treatments.

摘要

在过去的十年中,人们越来越关注微生物群和胆汁酸代谢之间的相互作用。胆汁酸不仅参与营养物质的代谢,而且在宿主生理活动的信号转导中也起着重要作用。微生物调节的胆汁酸代谢已被证明会影响许多疾病,但关于微生物受体信号通路对疾病调节的研究还很少。本综述考虑了最近关于法尼醇 X 受体 (FXR)、G 蛋白偶联胆汁酸受体 (TGR5)和维生素 D 受体 (VDR)信号通路在健康和疾病中微生物-宿主相互作用中的核心作用的研究结果。研究这些途径之间的关系可以帮助我们了解人类疾病的发病机制,并为其治疗提供新的解决方案。

相似文献

1
Regulation of bile acid metabolism-related signaling pathways by gut microbiota in diseases.肠道微生物群在疾病中对胆汁酸代谢相关信号通路的调控。
J Zhejiang Univ Sci B. 2019;20(10):781-792. doi: 10.1631/jzus.B1900073.
2
Bile Acid-Activated Receptors, Intestinal Microbiota, and the Treatment of Metabolic Disorders.胆汁酸激活受体、肠道微生物群与代谢紊乱的治疗。
Trends Mol Med. 2015 Nov;21(11):702-714. doi: 10.1016/j.molmed.2015.09.001. Epub 2015 Oct 16.
3
Intestine farnesoid X receptor agonist and the gut microbiota activate G-protein bile acid receptor-1 signaling to improve metabolism.肠法尼醇 X 受体激动剂和肠道微生物群激活 G 蛋白胆汁酸受体-1 信号通路以改善代谢。
Hepatology. 2018 Oct;68(4):1574-1588. doi: 10.1002/hep.29857. Epub 2018 May 21.
4
The Role of the Gut Microbiota in Bile Acid Metabolism.肠道微生物群在胆汁酸代谢中的作用。
Ann Hepatol. 2017 Nov;16(Suppl. 1: s3-105.):s15-s20. doi: 10.5604/01.3001.0010.5494.
5
Interactions between gut bacteria and bile in health and disease.肠道细菌与胆汁在健康与疾病中的相互作用。
Mol Aspects Med. 2017 Aug;56:54-65. doi: 10.1016/j.mam.2017.06.002. Epub 2017 Jun 21.
6
Bile Acid Control of Metabolism and Inflammation in Obesity, Type 2 Diabetes, Dyslipidemia, and Nonalcoholic Fatty Liver Disease.胆汁酸调控肥胖、2 型糖尿病、血脂异常和非酒精性脂肪性肝病中的代谢和炎症。
Gastroenterology. 2017 May;152(7):1679-1694.e3. doi: 10.1053/j.gastro.2017.01.055. Epub 2017 Feb 15.
7
Interaction of gut microbiota with dysregulation of bile acids in the pathogenesis of nonalcoholic fatty liver disease and potential therapeutic implications of probiotics.肠道微生物群与胆汁酸失调在非酒精性脂肪性肝病发病机制中的相互作用及益生菌的潜在治疗意义。
J Cell Biochem. 2019 Mar;120(3):2713-2720. doi: 10.1002/jcb.27635. Epub 2018 Nov 15.
8
Crosstalk between Bile Acids and Gut Microbiota and Its Impact on Farnesoid X Receptor Signalling.胆汁酸与肠道微生物群之间的相互作用及其对法尼醇X受体信号传导的影响
Dig Dis. 2017;35(3):246-250. doi: 10.1159/000450982. Epub 2017 Mar 1.
9
Bile Acid Modifications at the Microbe-Host Interface: Potential for Nutraceutical and Pharmaceutical Interventions in Host Health.在微生物-宿主界面的胆汁酸修饰:营养保健品和药物干预宿主健康的潜力。
Annu Rev Food Sci Technol. 2016;7:313-33. doi: 10.1146/annurev-food-041715-033159. Epub 2016 Jan 11.
10
Interactions between bile salts, gut microbiota, and hepatic innate immunity.胆汁盐、肠道微生物群和肝脏先天免疫之间的相互作用。
Immunol Rev. 2017 Sep;279(1):23-35. doi: 10.1111/imr.12579.

引用本文的文献

1
From Gut to Lung: The Role of Bile Acids in Rheumatoid Arthritis-Associated Interstitial Lung Disease (RA-ILD).从肠道到肺部:胆汁酸在类风湿关节炎相关间质性肺病(RA-ILD)中的作用
J Inflamm Res. 2025 Aug 2;18:10331-10340. doi: 10.2147/JIR.S524111. eCollection 2025.
2
Bile acids and gestational diabetes mellitus: exploring the link and implications - a review.胆汁酸与妊娠期糖尿病:探索两者之间的联系及影响——综述
Front Endocrinol (Lausanne). 2025 Jul 10;16:1574228. doi: 10.3389/fendo.2025.1574228. eCollection 2025.
3
The relationship between gut microbiome and human diseases: mechanisms, predisposing factors and potential intervention.肠道微生物群与人类疾病之间的关系:机制、易感因素和潜在干预措施。
Front Cell Infect Microbiol. 2025 May 6;15:1516010. doi: 10.3389/fcimb.2025.1516010. eCollection 2025.
4
Tetrahydrocurcumin Alleviates Metabolic Dysfunction-Associated Steatohepatitis in Mice by Regulating Serum Lipids, Bile Acids, and Gut Microbiota.四氢姜黄素通过调节血清脂质、胆汁酸和肠道微生物群减轻小鼠代谢功能障碍相关脂肪性肝炎。
Int J Mol Sci. 2025 Jan 22;26(3):895. doi: 10.3390/ijms26030895.
5
Perspectives on the involvement of the gut microbiota in salt-sensitive hypertension.肠道微生物群在盐敏感性高血压中的作用的观点。
Hypertens Res. 2024 Sep;47(9):2351-2362. doi: 10.1038/s41440-024-01747-y. Epub 2024 Jun 14.
6
Metabolomic signatures of intestinal colonization resistance against in mice.小鼠肠道定植抵抗对[具体对象未给出]的代谢组学特征。
Front Microbiol. 2023 Dec 18;14:1331114. doi: 10.3389/fmicb.2023.1331114. eCollection 2023.
7
Effects of Different Types of Dietary Fibers on Lipid Metabolism and Bile Acids in Weaned Piglets.不同类型膳食纤维对断奶仔猪脂质代谢和胆汁酸的影响
Animals (Basel). 2023 Oct 19;13(20):3266. doi: 10.3390/ani13203266.
8
The role of intestinal microbes on intestinal barrier function and host immunity from a metabolite perspective.从代谢物角度看肠道微生物对肠道屏障功能和宿主免疫的作用。
Front Immunol. 2023 Oct 9;14:1277102. doi: 10.3389/fimmu.2023.1277102. eCollection 2023.
9
Secondary bile acids function through the vitamin D receptor in myeloid progenitors to promote myelopoiesis.次级胆汁酸通过维生素 D 受体在髓系祖细胞中发挥作用,促进髓系细胞生成。
Blood Adv. 2023 Sep 12;7(17):4970-4982. doi: 10.1182/bloodadvances.2022009618.
10
The Implication of Mechanistic Approaches and the Role of the Microbiome in Polycystic Ovary Syndrome (PCOS): A Review.多囊卵巢综合征(PCOS)中机制性方法的意义及微生物组的作用:综述
Metabolites. 2023 Jan 14;13(1):129. doi: 10.3390/metabo13010129.

本文引用的文献

1
Bile-ology: from bench to bedside.胆学:从基础到临床。
J Zhejiang Univ Sci B. 2019 May;20(5):414-427. doi: 10.1631/jzus.B1900158.
2
A role for methanogens and methane in the regulation of GLP-1.产甲烷菌和甲烷在胰高血糖素样肽-1调节中的作用。
Endocrinol Diabetes Metab. 2017 Dec 1;1(1):e00006. doi: 10.1002/edm2.6. eCollection 2018 Jan.
3
Gut adaptation after metabolic surgery and its influences on the brain, liver and cancer.代谢手术后的肠道适应性及其对大脑、肝脏和癌症的影响。
Nat Rev Gastroenterol Hepatol. 2018 Oct;15(10):606-624. doi: 10.1038/s41575-018-0057-y.
4
New insights into bacterial bile resistance mechanisms: the role of bile salt hydrolase and its impact on human health.深入了解细菌耐胆汁机制:胆盐水解酶的作用及其对人类健康的影响。
Food Res Int. 2018 Oct;112:250-262. doi: 10.1016/j.foodres.2018.06.035. Epub 2018 Jun 20.
5
Functional microbiomics: Evaluation of gut microbiota-bile acid metabolism interactions in health and disease.功能微生物组学:健康与疾病中肠道微生物群-胆汁酸代谢相互作用的评估。
Methods. 2018 Oct 1;149:49-58. doi: 10.1016/j.ymeth.2018.04.028. Epub 2018 Apr 26.
6
Bile acid metabolism regulated by the gut microbiota promotes non-alcoholic steatohepatitis-associated hepatocellular carcinoma in mice.由肠道微生物群调节的胆汁酸代谢促进小鼠非酒精性脂肪性肝炎相关的肝细胞癌。
Oncotarget. 2018 Jan 6;9(11):9925-9939. doi: 10.18632/oncotarget.24066. eCollection 2018 Feb 9.
7
Intestine farnesoid X receptor agonist and the gut microbiota activate G-protein bile acid receptor-1 signaling to improve metabolism.肠法尼醇 X 受体激动剂和肠道微生物群激活 G 蛋白胆汁酸受体-1 信号通路以改善代谢。
Hepatology. 2018 Oct;68(4):1574-1588. doi: 10.1002/hep.29857. Epub 2018 May 21.
8
Microbiota-Derived Indole Metabolites Promote Human and Murine Intestinal Homeostasis through Regulation of Interleukin-10 Receptor.微生物衍生吲哚代谢物通过调节白细胞介素-10 受体促进人和鼠类肠道内稳态
Am J Pathol. 2018 May;188(5):1183-1194. doi: 10.1016/j.ajpath.2018.01.011. Epub 2018 Feb 16.
9
Review article: the gut microbiome as a therapeutic target in the pathogenesis and treatment of chronic liver disease.综述文章:肠道微生物组作为慢性肝病发病机制和治疗的治疗靶点。
Aliment Pharmacol Ther. 2018 Jan;47(2):192-202. doi: 10.1111/apt.14397. Epub 2017 Oct 30.
10
Nuclear receptor FXR, bile acids and liver damage: Introducing the progressive familial intrahepatic cholestasis with FXR mutations.核受体 FXR、胆汁酸和肝损伤:介绍伴有 FXR 突变的进行性家族性肝内胆汁淤积症。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1308-1318. doi: 10.1016/j.bbadis.2017.09.019. Epub 2017 Sep 29.