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Diversification of host bile acids by members of the gut microbiota

机译:肠道微生物成员的宿主胆汁酸多样化

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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.
机译:胆汁酸生物转化是宿主和肠道微生物组的合作效果。 宿主肝细胞用胆固醇合成原发性胆汁酸。 一旦这些宿主衍生的原发性胆汁酸进入胃肠道,肠道微生物会将它们化学改性它们进入二次胆汁酸。 肠胆酸宿主轴的兴趣在不同的领域中扩展,包括胃肠病学,内分泌,肿瘤学和传染病。 本综述旨在1)描述宿主和肠道微生物的协同胆汁酸代谢的生理方面; 2)评估肠道微生物如何影响胆汁酸池,并且又转过胆汁酸池如何调节肠道微生物群落结构; 3)比较胆汁酸池的物种差异; 最后,4)讨论甲羟氧胆酸(UDCA)给药,常见的治疗胆汁酸,肠道微生物酸胆酸宿主轴的影响。

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