Gut Microbiota at the Crossroad of Hepatic Oxidative Stress and MASLD.

IF 6.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Antioxidants Pub Date : 2025-01-06 DOI:10.3390/antiox14010056
Fabrizio Termite, Sebastiano Archilei, Francesca D'Ambrosio, Lucrezia Petrucci, Nicholas Viceconti, Roberta Iaccarino, Antonio Liguori, Antonio Gasbarrini, Luca Miele
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Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent chronic liver condition marked by excessive lipid accumulation in hepatic tissue. This disorder can lead to a range of pathological outcomes, including metabolic dysfunction-associated steatohepatitis (MASH) and cirrhosis. Despite extensive research, the molecular mechanisms driving MASLD initiation and progression remain incompletely understood. Oxidative stress and lipid peroxidation are pivotal in the "multiple parallel hit model", contributing to hepatic cell death and tissue damage. Gut microbiota plays a substantial role in modulating hepatic oxidative stress through multiple pathways: impairing the intestinal barrier, which results in bacterial translocation and chronic hepatic inflammation; modifying bile acid structure, which impacts signaling cascades involved in lipidic metabolism; influencing hepatocytes' ferroptosis, a form of programmed cell death; regulating trimethylamine N-oxide (TMAO) metabolism; and activating platelet function, both recently identified as pathogenetic factors in MASH progression. Moreover, various exogenous factors impact gut microbiota and its involvement in MASLD-related oxidative stress, such as air pollution, physical activity, cigarette smoke, alcohol, and dietary patterns. This manuscript aims to provide a state-of-the-art overview focused on the intricate interplay between gut microbiota, lipid peroxidation, and MASLD pathogenesis, offering insights into potential strategies to prevent disease progression and its associated complications.

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肝脏氧化应激与MASLD交叉路口的肠道菌群。
代谢功能障碍相关的脂肪变性肝病(MASLD)是一种常见的慢性肝病,其特征是肝组织中脂肪堆积过多。这种疾病可导致一系列病理结果,包括代谢功能障碍相关的脂肪性肝炎(MASH)和肝硬化。尽管进行了广泛的研究,但驱动MASLD发生和进展的分子机制仍然不完全清楚。氧化应激和脂质过氧化在“多重平行撞击模型”中起关键作用,导致肝细胞死亡和组织损伤。肠道菌群通过多种途径在调节肝脏氧化应激中发挥重要作用:损害肠道屏障,导致细菌易位和慢性肝脏炎症;改变胆汁酸结构,影响脂质代谢的信号级联反应;影响肝细胞铁下垂,一种程序性细胞死亡;调节三甲胺n -氧化物(TMAO)代谢;和激活血小板功能,这两者最近都被确定为MASH进展的致病因素。此外,多种外源性因素影响肠道微生物群及其参与masld相关的氧化应激,如空气污染、体育活动、吸烟、酒精和饮食模式。本文旨在提供最新的概述,重点关注肠道微生物群,脂质过氧化和MASLD发病机制之间复杂的相互作用,为预防疾病进展及其相关并发症的潜在策略提供见解。
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来源期刊
Antioxidants
Antioxidants Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
10.60
自引率
11.40%
发文量
2123
审稿时长
16.3 days
期刊介绍: Antioxidants (ISSN 2076-3921), provides an advanced forum for studies related to the science and technology of antioxidants. It publishes research papers, reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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