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肠道微生物衍生成分和代谢物在非酒精性脂肪性肝病(NAFLD)进展中的作用。

Gut Microbiota-Derived Components and Metabolites in the Progression of Non-Alcoholic Fatty Liver Disease (NAFLD).

机构信息

Department of Physiology and Pathophysiology, Peking University Health Science Center, Beijing 100191, China.

Department of Surgery, University of Michigan Medical Center, Ann Arbor, MI 48109-0346, USA.

出版信息

Nutrients. 2019 Jul 25;11(8):1712. doi: 10.3390/nu11081712.

Abstract

Human gut microbiota has been increasingly recognized as a pivotal determinant of non-alcoholic fatty liver disease (NAFLD). Apart from the changes in the composition of gut microbiota, the components and metabolites derived from intestinal microbiota have emerged as key factors in modulating the pathological process of NAFLD. Compelling evidences have revealed that gut microbiota generates a variety of bioactive substances that interact with the host liver cells through the portal vein. These substances include the components derived from bacteria such as lipopolysaccharides, peptidoglycan, DNA, and extracellular vesicles, as well as the metabolites ranging from short-chain fatty acids, indole and its derivatives, trimethylamine, secondary bile acids, to carotenoids and phenolic compounds. The mechanisms underlying the hepatic responses to the bioactive substances from gut bacteria have been associated with the regulation of glycolipid metabolism, immune signaling response, and redox homeostasis. Illuminating the interplay between the unique factors produced from gut microbiome and the liver will provide a novel therapeutical target for NAFLD. The current review highlights the recent advances on the mechanisms by which the key ingredients and metabolites from gut microbiota modulate the development and progression of NAFLD.

摘要

人类肠道微生物群已被越来越多地认为是非酒精性脂肪性肝病(NAFLD)的关键决定因素。除了肠道微生物群组成的变化外,源自肠道微生物群的成分和代谢物已成为调节 NAFLD 病理过程的关键因素。令人信服的证据表明,肠道微生物群产生各种生物活性物质,通过门静脉与宿主肝细胞相互作用。这些物质包括源自细菌的成分,如脂多糖、肽聚糖、DNA 和细胞外囊泡,以及代谢物,范围从短链脂肪酸、吲哚及其衍生物、三甲胺、次级胆汁酸到类胡萝卜素和酚类化合物。肠道细菌的生物活性物质引起肝脏反应的机制与糖脂代谢、免疫信号反应和氧化还原平衡的调节有关。阐明来自肠道微生物组的独特因素与肝脏之间的相互作用将为 NAFLD 提供新的治疗靶点。本综述重点介绍了肠道微生物群的关键成分和代谢物调节 NAFLD 发生和发展的机制的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc14/6724003/a552e6f6e5bf/nutrients-11-01712-g001.jpg

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