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7-α-脱羟基化途径:肠道细菌胆汁酸代谢的一个组成部分及潜在治疗靶点。

The 7-α-dehydroxylation pathway: An integral component of gut bacterial bile acid metabolism and potential therapeutic target.

作者信息

Wise Journey L, Cummings Bethany P

机构信息

Department of Biomedical Sciences, Cornell University, Ithaca, NY, United States.

Department of Surgery, Center for Alimentary and Metabolic Sciences, School of Medicine, University of California, Davis, Sacramento, CA, United States.

出版信息

Front Microbiol. 2023 Jan 9;13:1093420. doi: 10.3389/fmicb.2022.1093420. eCollection 2022.

Abstract

The gut microbiome plays a significant role in maintaining host metabolic health through the production of metabolites. Comprising one of the most abundant and diverse forms of gut metabolites, bile acids play a key role in blood glucose regulation, insulin sensitivity, obesity, and energy expenditure. A central pathway in gut bacterial bile acid metabolism is the production of secondary bile acids 7-ɑ-dehydroxylation. Despite the important role of 7-ɑ-dehydroxylation in gut bacterial bile acid metabolism and the pathophysiology of metabolic disease, the regulation of this pathway is not completely understood. This review aims to outline our current understanding of 7-ɑ-dehydroxylation and to identify key knowledge gaps that will be integral in further characterizing gut bacterial bile acid metabolism as a potential therapeutic target for treating metabolic dysregulation.

摘要

肠道微生物群通过产生代谢物在维持宿主代谢健康方面发挥着重要作用。胆汁酸是肠道代谢物中最丰富、最多样化的形式之一,在血糖调节、胰岛素敏感性、肥胖和能量消耗中起关键作用。肠道细菌胆汁酸代谢的一条核心途径是次级胆汁酸7-α-脱羟基化的产生。尽管7-α-脱羟基化在肠道细菌胆汁酸代谢和代谢疾病的病理生理学中具有重要作用,但该途径的调节尚未完全了解。本综述旨在概述我们目前对7-α-脱羟基化的理解,并确定关键的知识空白,这些空白对于进一步将肠道细菌胆汁酸代谢表征为治疗代谢失调的潜在治疗靶点至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa72/9868651/8e5d8e233e4b/fmicb-13-1093420-g001.jpg

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