Li Li, Hu Ying, Wang Yu-Mei, Wu Xiao-Xue, Lin Si-Tong, Li Hang, Zhang Ji, Fan Guo-Rong, Wang Zong-De, Wang Bin, Chen Shang-Xing
East China Woody Fragrance and Flavor Engineering Technology Research Center of National Forestry and Grassland Administration, College of Forestry, Jiangxi Agricultural University, Nanchang 330045, China.
Jiangxi Provincial Key Laboratory of Improved Variety Breeding and Efficient Utilization of Native Tree Species, Nanchang 330045, China.
Foods. 2025 May 12;14(10):1707. doi: 10.3390/foods14101707.
In this study, we systematically investigated the mechanisms of the antioxidation and anti-lipid accumulation effects of antioxidant peptides from on a free fatty acid (FFA)-induced NAFLD model of HepG2 cells. The NAFLD cell model was constructed by inducing the HepG2 hepatocellular carcinoma cell line with 0.5 mmol/L FFAs, and AQRDAGLL, QEGPFVR, and DVPPPRGPL were given to the culture to study their lipid-lowering and antioxidant activities on NAFLD cells. The lipid-lowering activities of the three antioxidant peptides were evaluated by Oil Red O staining and TG and TC content assays, and the results showed that all three peptides had strong ameliorating effects on FFA-induced lipid accumulation in NAFLD cells. The intracellular antioxidant protease (CAT, GSH, and SOD) activity levels and lipid peroxidation (MDA) content were measured and intracellular ROS levels were detected. The results showed that after intervention with the antioxidant peptides, the intracellular ROS levels in the NAFLD model cells were significantly reduced, the SOD and CAT activities were increased, the GSH content was elevated, and the MDA content was reduced, which indicated that AQRDAGLL, QEGPFVR, and DVPPPRGPL were able to inhibit the oxidative stress of the cells effectively and to achieve the effect of intervening in NAFLD. JC-1 fluorescence staining experiments showed that the mitochondrial membrane potential function of NAFLD cells was restored under the effect of the antioxidant peptides. Molecular dynamics simulations revealed that the main driving force between QEGPFVR and Keap1 protein was van der Waals forces, ΔG = -62.11 kcal/mol, which indicated that QEGPFVR was capable of spontaneously binding to Keap1 protein.
在本研究中,我们系统地研究了抗氧化肽对游离脂肪酸(FFA)诱导的HepG2细胞非酒精性脂肪性肝病(NAFLD)模型的抗氧化和抗脂质积累作用机制。通过用0.5 mmol/L FFA诱导HepG2肝癌细胞系构建NAFLD细胞模型,并将AQRDAGLL、QEGPFVR和DVPPPRGPL加入培养液中,研究它们对NAFLD细胞的降脂和抗氧化活性。通过油红O染色以及甘油三酯(TG)和总胆固醇(TC)含量测定评估这三种抗氧化肽的降脂活性,结果表明所有三种肽对FFA诱导的NAFLD细胞脂质积累均有较强的改善作用。测定细胞内抗氧化蛋白酶(CAT、GSH和SOD)活性水平以及脂质过氧化(MDA)含量,并检测细胞内活性氧(ROS)水平。结果显示,抗氧化肽干预后,NAFLD模型细胞内ROS水平显著降低,SOD和CAT活性增加,GSH含量升高,MDA含量降低,这表明AQRDAGLL、QEGPFVR和DVPPPRGPL能够有效抑制细胞的氧化应激,从而达到干预NAFLD的效果。JC-1荧光染色实验表明,在抗氧化肽的作用下,NAFLD细胞的线粒体膜电位功能得以恢复。分子动力学模拟显示,QEGPFVR与Keap1蛋白之间的主要驱动力是范德华力,ΔG = -62.11 kcal/mol,这表明QEGPFVR能够自发地与Keap1蛋白结合。