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肠道细菌对胆盐生物转化的后果。

Consequences of bile salt biotransformations by intestinal bacteria.

作者信息

Ridlon Jason M, Harris Spencer C, Bhowmik Shiva, Kang Dae-Joong, Hylemon Phillip B

机构信息

a Department of Animal Sciences , University of Illinois Urbana-Champaign , Urbana , IL , USA.

b Department of Microbiology and Immunology , Virginia Commonwealth University , Richmond , VA , USA.

出版信息

Gut Microbes. 2016;7(1):22-39. doi: 10.1080/19490976.2015.1127483.

DOI:10.1080/19490976.2015.1127483
PMID:26939849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4856454/
Abstract

Emerging evidence strongly suggest that the human "microbiome" plays an important role in both health and disease. Bile acids function both as detergents molecules promoting nutrient absorption in the intestines and as hormones regulating nutrient metabolism. Bile acids regulate metabolism via activation of specific nuclear receptors (NR) and G-protein coupled receptors (GPCRs). The circulating bile acid pool composition consists of primary bile acids produced from cholesterol in the liver, and secondary bile acids formed by specific gut bacteria. The various biotransformation of bile acids carried out by gut bacteria appear to regulate the structure of the gut microbiome and host physiology. Increased levels of secondary bile acids are associated with specific diseases of the GI system. Elucidating methods to control the gut microbiome and bile acid pool composition in humans may lead to a reduction in some of the major diseases of the liver, gall bladder and colon.

摘要

新出现的证据有力地表明,人类“微生物群”在健康和疾病中都起着重要作用。胆汁酸既作为促进肠道营养吸收的洗涤剂分子,又作为调节营养代谢的激素发挥作用。胆汁酸通过激活特定的核受体(NR)和G蛋白偶联受体(GPCR)来调节代谢。循环胆汁酸池的组成包括肝脏中由胆固醇产生的初级胆汁酸,以及由特定肠道细菌形成的次级胆汁酸。肠道细菌对胆汁酸进行的各种生物转化似乎调节着肠道微生物群的结构和宿主生理。次级胆汁酸水平升高与胃肠道系统的特定疾病有关。阐明控制人类肠道微生物群和胆汁酸池组成的方法可能会减少一些肝脏、胆囊和结肠的主要疾病。

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本文引用的文献

1
Structure and functional characterization of a bile acid 7α dehydratase BaiE in secondary bile acid synthesis.次级胆汁酸合成中胆汁酸7α脱水酶BaiE的结构与功能表征
Proteins. 2016 Mar;84(3):316-31. doi: 10.1002/prot.24971. Epub 2016 Jan 18.
2
The human gut sterolbiome: bile acid-microbiome endocrine aspects and therapeutics.人类肠道固醇生物群落:胆汁酸 - 微生物群落的内分泌方面及治疗学
Acta Pharm Sin B. 2015 Mar;5(2):99-105. doi: 10.1016/j.apsb.2015.01.006. Epub 2015 Feb 9.
3
A biosynthetic pathway for a prominent class of microbiota-derived bile acids.一类主要的微生物群衍生胆汁酸的生物合成途径。
Nat Chem Biol. 2015 Sep;11(9):685-90. doi: 10.1038/nchembio.1864. Epub 2015 Jul 20.
4
Fat, fibre and cancer risk in African Americans and rural Africans.非裔美国人和非洲农村居民的脂肪、纤维与癌症风险
Nat Commun. 2015 Apr 28;6:6342. doi: 10.1038/ncomms7342.
5
Burden of Clostridium difficile infection in the United States.美国艰难梭菌感染的负担
N Engl J Med. 2015 Feb 26;372(9):825-34. doi: 10.1056/NEJMoa1408913.
6
Bile acids as metabolic regulators.胆汁酸作为代谢调节剂。
Curr Opin Gastroenterol. 2015 Mar;31(2):159-65. doi: 10.1097/MOG.0000000000000156.
7
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile.精准微生物群重建可恢复胆汁酸介导的对艰难梭菌的抗性。
Nature. 2015 Jan 8;517(7533):205-8. doi: 10.1038/nature13828. Epub 2014 Oct 22.
8
Functional role of tlyC1 encoding a hemolysin-like protein from Bifidobacterium longum BBMN68 in bile tolerance.长双歧杆菌BBMN68中编码类溶血素蛋白的tlyC1在胆汁耐受性中的功能作用。
FEMS Microbiol Lett. 2014 Nov;360(2):167-73. doi: 10.1111/1574-6968.12601. Epub 2014 Oct 21.
9
Intestinal transport and metabolism of bile acids.胆汁酸的肠道转运与代谢
J Lipid Res. 2015 Jun;56(6):1085-99. doi: 10.1194/jlr.R054114. Epub 2014 Sep 10.
10
Ursodeoxycholic acid ameliorates fructose-induced metabolic syndrome in rats.熊去氧胆酸改善果糖诱导的大鼠代谢综合征。
PLoS One. 2014 Sep 9;9(9):e106993. doi: 10.1371/journal.pone.0106993. eCollection 2014.