MCFA alleviate H2O2-induced oxidative stress in AML12 cells via the ERK1/2/Nrf2 pathway

IF 1.8 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lipids Pub Date : 2022-03-09 DOI:10.1002/lipd.12339
Danping Wang, Jinglong Chen, Huangbing Sun, Wenjing Chen, Xiaojing Yang
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引用次数: 5

Abstract

Oxidative stress is an important factor in the occurrence and development of liver disease. Medium-chain fatty acids (MCFAs) have potential antioxidant function, whereas the exact underlying mechanism of MCFA in oxidative injury of hepatocytes remains unclear. In our present study, three different MCFAs, 8-carbon octanoic acid (OA), 10-carbon capric acid (CA), and 12-carbon lauric acid (LA), have been performed to observe their protective action for hepatocyte under the H2O2 challenge. The result showed that MCFA treatment significantly increased the cell viability, T-AOC, and expression of antioxidant-related genes in AML12 cells under oxidative stress condition, and reduced reactive oxygen species (ROS) production. Moreover, MCFA treatment significantly increased the protein expression of Nrf2 and the phosphorylation level of ERK1/2; LA treatment significantly promoted the Nrf2 nuclear translocation. With a further test, the rescue ability of MCFA was blocked by treating with the ERK inhibitor U0126. Overall, our data suggested that MCFA treatment has positive impact on protecting AML12 cells against oxidative stress through ERK1/2/Nrf2 pathway.

MCFA通过ERK1/2/Nrf2途径缓解h2o2诱导的AML12细胞氧化应激
氧化应激是肝脏疾病发生发展的重要因素。中链脂肪酸(MCFAs)具有潜在的抗氧化功能,但MCFA在肝细胞氧化损伤中的确切机制尚不清楚。本研究采用8碳辛酸(OA)、10碳癸酸(CA)和12碳月桂酸(LA)三种不同的MCFAs,观察它们在H2O2胁迫下对肝细胞的保护作用。结果表明,MCFA处理显著提高了氧化应激条件下AML12细胞的细胞活力、T-AOC和抗氧化相关基因的表达,减少了活性氧(ROS)的产生。此外,MCFA处理显著提高Nrf2蛋白表达和ERK1/2磷酸化水平;LA处理显著促进Nrf2核易位。在进一步的实验中,ERK抑制剂U0126可以阻断MCFA的拯救能力。总的来说,我们的数据表明MCFA处理通过ERK1/2/Nrf2途径对保护AML12细胞抗氧化应激具有积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lipids
Lipids 生物-生化与分子生物学
CiteScore
4.20
自引率
5.30%
发文量
33
审稿时长
4-8 weeks
期刊介绍: Lipids is a journal of the American Oil Chemists'' Society (AOCS) that focuses on publishing high-quality peer-reviewed papers and invited reviews in the general area of lipid research, including chemistry, biochemistry, clinical nutrition, and metabolism. In addition, Lipids publishes papers establishing novel methods for addressing research questions in the field of lipid research.
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