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内源性乙醇代谢与代谢相关脂肪性肝病-脂肪性肝炎的发展

Endogenous Ethanol Metabolism and Development of MASLD-MASH.

作者信息

Farràs Solé Núria, Wydh Sander, Alizadeh Bahmani Amir Hossein, Bui Thi Phuong Nam, Nieuwdorp Max

机构信息

Department of Experimental Vascular Medicine, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.

Department of Internal and Vascular Medicine, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.

出版信息

Int J Mol Sci. 2025 Sep 4;26(17):8609. doi: 10.3390/ijms26178609.

DOI:10.3390/ijms26178609
PMID:40943542
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12428997/
Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is an increasingly prevalent liver disorder driven by metabolic dysregulation and inflammation. Recent studies highlight the importance of the gut microbiome as a key contributor to this pathology through its ability to ferment dietary sugars into ethanol, a metabolite previously overlooked in MASLD. In this review, we discuss the role of the gut microbiome in MASLD, covering functional and compositional shifts observed in the disease; we dive into the different microbial pathways of ethanol synthesis, hepatic mechanisms of ethanol clearance, and pathological consequences. We also discuss the role of a healthy microbiome in the clearance of ethanol in the gut and how microbiome-based strategies could be beneficial in targeting endogenous production of ethanol, going from the traditional probiotic-prebiotic combination to discussing new approaches.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)是一种由代谢失调和炎症驱动的日益普遍的肝脏疾病。最近的研究强调了肠道微生物群作为这种病理状态关键促成因素的重要性,因为它能够将膳食糖发酵成乙醇,这是一种以前在MASLD中被忽视的代谢物。在这篇综述中,我们讨论了肠道微生物群在MASLD中的作用,涵盖了在该疾病中观察到的功能和组成变化;我们深入探讨了乙醇合成的不同微生物途径、乙醇清除的肝脏机制以及病理后果。我们还讨论了健康微生物群在肠道中清除乙醇的作用,以及基于微生物群的策略如何可能有利于针对内源性乙醇产生,从传统的益生菌 - 益生元组合到讨论新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/389820a211eb/ijms-26-08609-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/c1e5a34ac7ac/ijms-26-08609-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/cbb2bae81f5b/ijms-26-08609-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/4c011c43bde0/ijms-26-08609-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/389820a211eb/ijms-26-08609-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/c1e5a34ac7ac/ijms-26-08609-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/cbb2bae81f5b/ijms-26-08609-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/4c011c43bde0/ijms-26-08609-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/12428997/389820a211eb/ijms-26-08609-g004.jpg

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本文引用的文献

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2
Prolonged Intestinal Ethanol Absorption and Oxidative Stress: Revisiting the Gut-Liver Axis in Alcohol-Associated Disease.肠道对乙醇的持续吸收与氧化应激:重新审视酒精相关疾病中的肠-肝轴
Int J Mol Sci. 2025 Jun 6;26(12):5442. doi: 10.3390/ijms26125442.
3
Enterotype-stratified gut microbial signatures in MASLD and cirrhosis based on integrated microbiome data.
基于整合微生物组数据的非酒精性脂肪性肝病和肝硬化中肠型分层的肠道微生物特征
Front Microbiol. 2025 May 15;16:1568672. doi: 10.3389/fmicb.2025.1568672. eCollection 2025.
4
Characterization of gut dysbiosis and intestinal barrier dysfunction in patients with metabolic dysfunction-associated steatotic liver disease and chronic kidney disease: a comparative study.代谢功能障碍相关脂肪性肝病和慢性肾脏病患者肠道菌群失调及肠屏障功能障碍的特征:一项比较研究
Sci Rep. 2025 May 3;15(1):15481. doi: 10.1038/s41598-025-00237-6.
5
Full-length 16S rRNA Sequencing Reveals Gut Microbiome Signatures Predictive of MASLD in children with obesity.全长16S rRNA测序揭示了可预测肥胖儿童代谢相关脂肪性肝病的肠道微生物群特征。
BMC Microbiol. 2025 Mar 17;25(1):146. doi: 10.1186/s12866-025-03849-0.
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Multi-omics analyses of the gut microbiota and metabolites in children with metabolic dysfunction-associated steatotic liver disease.代谢功能障碍相关脂肪性肝病患儿肠道微生物群和代谢物的多组学分析
mSystems. 2025 Apr 22;10(4):e0114824. doi: 10.1128/msystems.01148-24. Epub 2025 Mar 14.
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Front Nutr. 2025 Feb 19;12:1500293. doi: 10.3389/fnut.2025.1500293. eCollection 2025.
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