Diversification of host bile acids by members of the gut microbiota

被引:347
|
作者
Winston, Jenessa A. [1 ,2 ]
Theriot, Casey M. [1 ]
机构
[1] North Carolina State Univ, Dept Populat Hlth & Pathobiol, Coll Vet Med, Res Bldg 406,1060 William Moore Dr, Raleigh, NC 27607 USA
[2] Ohio State Univ, Coll Vet Med, Dept Vet Clin Sci, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
C; difficile; bile acids; gut microbiota; ursodeoxycholic acid (UDCA); FXR; DIFFICILE SPORE GERMINATION; PRIMARY BILIARY-CIRRHOSIS; URSODEOXYCHOLIC ACID; 7-BETA-HYDROXYSTEROID DEHYDROGENASE; INTESTINAL MICROBIOTA; PEPTOSTREPTOCOCCUS-PRODUCTUS; ENTEROHEPATIC CIRCULATION; CHENODEOXYCHOLIC ACID; CONNECTING DYSBIOSIS; METABOLIC PROFILES;
D O I
10.1080/19490976.2019.1674124
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Bile acid biotransformation is a collaborative effort by the host and the gut microbiome. Host hepatocytes synthesize primary bile acids from cholesterol. Once these host-derived primary bile acids enter the gastrointestinal tract, the gut microbiota chemically modify them into secondary bile acids. Interest into the gut-bile acid-host axis is expanding in diverse fields including gastroenterology, endocrinology, oncology, and infectious disease. This review aims to 1) describe the physiologic aspects of collaborative bile acid metabolism by the host and gut microbiota; 2) to evaluate how gut microbes influence bile acid pools, and in turn how bile acid pools modulate the gut microbial community structure; 3) to compare species differences in bile acid pools; and lastly, 4) discuss the effects of ursodeoxycholic acid (UDCA) administration, a common therapeutic bile acid, on the gut microbiota-bile acid-host axis.
引用
收藏
页码:158 / 171
页数:14
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