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肠道微生物群与代谢物界面介导的肝脏炎症。

Gut microbiota and metabolite interface-mediated hepatic inflammation.

作者信息

Yang Ming, Massad Katina, Kimchi Eric T, Staveley-O'Carroll Kevin F, Li Guangfu

机构信息

Department of Surgery, University of Missouri, Columbia, MO, USA.

NextGen Precision Health Institute, University of Missouri, Columbia, MO, USA.

出版信息

Immunometabolism (Cobham). 2024 Jan 25;6(1):e00037. doi: 10.1097/IN9.0000000000000037. eCollection 2024 Jan.

Abstract

Immunologic and metabolic signals regulated by gut microbiota and relevant metabolites mediate bidirectional interaction between the gut and liver. Gut microbiota dysbiosis, due to diet, lifestyle, bile acids, and genetic and environmental factors, can advance the progression of chronic liver disease. Commensal gut bacteria have both pro- and anti-inflammatory effects depending on their species and relative abundance in the intestine. Components and metabolites derived from gut microbiota-diet interaction can regulate hepatic innate and adaptive immune cells, as well as liver parenchymal cells, significantly impacting liver inflammation. In this mini review, recent findings of specific bacterial species and metabolites with functions in regulating liver inflammation are first reviewed. In addition, socioeconomic and environmental factors, hormones, and genetics that shape the profile of gut microbiota and microbial metabolites and components with the function of priming or dampening liver inflammation are discussed. Finally, current clinical trials evaluating the factors that manipulate gut microbiota to treat liver inflammation and chronic liver disease are reviewed. Overall, the discussion of microbial and metabolic mediators contributing to liver inflammation will help direct our future studies on liver disease.

摘要

由肠道微生物群和相关代谢产物调节的免疫和代谢信号介导了肠道与肝脏之间的双向相互作用。由于饮食、生活方式、胆汁酸以及遗传和环境因素导致的肠道微生物群失调,会加速慢性肝病的进展。共生肠道细菌根据其种类和在肠道中的相对丰度具有促炎和抗炎作用。源自肠道微生物群与饮食相互作用的成分和代谢产物可调节肝脏固有免疫细胞和适应性免疫细胞以及肝实质细胞,对肝脏炎症产生显著影响。在这篇小型综述中,首先回顾了具有调节肝脏炎症功能的特定细菌种类和代谢产物的最新研究发现。此外,还讨论了塑造肠道微生物群以及具有引发或减轻肝脏炎症功能的微生物代谢产物和成分的社会经济和环境因素、激素及遗传学。最后,对目前评估操纵肠道微生物群以治疗肝脏炎症和慢性肝病的因素的临床试验进行了综述。总体而言,对导致肝脏炎症的微生物和代谢介质的讨论将有助于指导我们未来对肝病的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4c/10810350/4d38926bab5d/in9-6-e00037-g001.jpg

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