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富氢水通过激活HepG2细胞中的AMP活化蛋白激酶减少脂肪酸诱导的脂质积累和氧化应激损伤。

Hydrogen-Rich Water (HRW) Reduces Fatty Acid-Induced Lipid Accumulation and Oxidative Stress Damage through Activating AMP-Activated Protein Kinase in HepG2 Cells.

作者信息

Tsou Sing-Hua, Lin Sheng-Chieh, Chen Wei-Jen, Hung Hui-Chih, Liao Chun-Cheng, Kornelius Edy, Huang Chien-Ning, Lin Chih-Li, Yang Yi-Sun

机构信息

Department of Medical Research, Chung Shan Medical University Hospital, Taichung 402, Taiwan.

School of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.

出版信息

Biomedicines. 2024 Jun 28;12(7):1444. doi: 10.3390/biomedicines12071444.

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by excessive fat accumulation in the liver. Intracellular oxidative stress induced by lipid accumulation leads to various hepatocellular injuries including fibrosis. However, no effective method for mitigating MASLD without substantial side effects currently exists. Molecular hydrogen (H) has garnered attention due to its efficiency in neutralizing harmful reactive oxygen species (ROS) and its ability to penetrate cell membranes. Some clinical evidence suggests that H may alleviate fatty liver disease, but the precise molecular mechanisms, particularly the regulation of lipid droplet (LD) metabolism, remain unclear. This study utilized an in vitro model of hepatocyte lipid accumulation induced by free fatty acids (FFAs) to replicate MASLD in HepG2 cells. The results demonstrated a significant increase in LD accumulation due to elevated FFA levels. However, the addition of hydrogen-rich water (HRW) effectively reduced LD accumulation. HRW decreased the diameter of LDs and reduced lipid peroxidation and FFA-induced oxidative stress by activating the AMPK/Nrf2/HO-1 pathway. Overall, our findings suggest that HRW has potential as an adjunctive supplement in managing fatty liver disease by reducing LD accumulation and enhancing antioxidant pathways, presenting a novel strategy for impeding MASLD progression.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)的特征是肝脏中脂肪过度积累。脂质积累诱导的细胞内氧化应激会导致包括纤维化在内的各种肝细胞损伤。然而,目前尚无有效且无明显副作用的减轻MASLD的方法。分子氢(H₂)因其在中和有害活性氧(ROS)方面的效率及其穿透细胞膜的能力而受到关注。一些临床证据表明,H₂可能减轻脂肪肝疾病,但确切的分子机制,特别是脂滴(LD)代谢的调节,仍不清楚。本研究利用游离脂肪酸(FFA)诱导的肝细胞脂质积累体外模型在HepG2细胞中复制MASLD。结果表明,由于FFA水平升高,LD积累显著增加。然而,添加富氢水(HRW)有效地减少了LD积累。HRW通过激活AMPK/Nrf2/HO-1途径降低了LD的直径,减少了脂质过氧化和FFA诱导的氧化应激。总体而言,我们的研究结果表明,HRW通过减少LD积累和增强抗氧化途径,有潜力作为管理脂肪肝疾病的辅助补充剂,为阻止MASLD进展提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b501/11274623/3783ded0759a/biomedicines-12-01444-g001.jpg

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