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鱼油与菊苣酸联合使用通过调节AMPK介导的SREBP-1/FAS和PPARα/UCP2途径,对棕榈酸酯诱导的脂质积累具有更好的保护作用。

Fish oil and chicoric acid combination protects better against palmitate-induced lipid accumulation via regulating AMPK-mediated SREBP-1/FAS and PPARα/UCP2 pathways.

作者信息

Mohammadi Mohammad, Abbasalipourkabir Roghayeh, Ziamajidi Nasrin

机构信息

Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Molecular Medicine Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

出版信息

Arch Physiol Biochem. 2023 Feb;129(1):1-9. doi: 10.1080/13813455.2020.1789881. Epub 2020 Jul 11.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is associated with lipid accumulation and lipotoxicity. The main aim of this study is to evaluate the synergistic treatment effect of fish oils (FOs) and chicoric acid (CA) in palmitate (PA)-induced NAFLD HepG2 model. HepG2 cells were pre-treated with palmitate (0.75 mM) for 24 h, and then were exposed to CA, FOs and combination of these chemicals for another 24 h. Gene expression and protein levels were determined using qRT-PCR and western blotting or ELISA analysing, respectively. The combination index (CI) values of FOs and CA in HepG2 cells were calculated according to the Chou-Talalay equation using the CompuSyn software. FOs and CA acid together synergistically reduced lipid accumulation as indicated by decreased oil red O staining (vehicle-treated control: 1 ± 0.1; PA-treated control: 4.7 ± 0.4; PA + CA100: 3.9 ± 0.4; PA + CA200: 2.4 ± 0.3; PA + FOs: 2.7 ± 0.1; PA + CA200 + FOs: 1.5 ± 0.1) and triglyceride (vehicle-treatedcontrol:10 ± 1.2; PA-treated control: 25.8 ± 2.7; PA + CA100: 18.9 ± 2.5; PA + CA200: 14.4 ± 1.8; PA + FOs: 15.2 ± 2.4; PA + CA200 + FOs: 11.9 ± 1.5) levels in PA-treated HepG2 cells. Gene expression and Immunoblotting analysis confirmed the combination effect of FOs and CA in up-regulation of AMPK-mediated PPARα/UCP2 and down-regulation of AMPK-mediated SREBP-1/FAS signalling pathways. Collectively, these results suggest that combining FOs with CA can serve as a potential combination therapy for NAFLD.

摘要

非酒精性脂肪性肝病(NAFLD)与脂质蓄积和脂毒性相关。本研究的主要目的是评估鱼油(FOs)和菊苣酸(CA)在棕榈酸(PA)诱导的NAFLD HepG2模型中的协同治疗效果。将HepG2细胞用棕榈酸(0.75 mM)预处理24小时,然后再将其暴露于CA、FOs以及这些化学物质的组合中24小时。分别使用qRT-PCR和蛋白质免疫印迹法或ELISA分析来测定基因表达和蛋白质水平。使用CompuSyn软件根据Chou-Talalay方程计算HepG2细胞中FOs和CA的组合指数(CI)值。如油红O染色减少所示(溶剂处理对照组:1±0.1;PA处理对照组:4.7±0.4;PA + CA100:3.9±0.4;PA + CA200:2.4±0.3;PA + FOs:2.7±0.1;PA + CA200 + FOs:1.5±0.1)以及PA处理的HepG2细胞中的甘油三酯水平(溶剂处理对照组:10±1.2;PA处理对照组:25.8±2.7;PA + CA100:18.9±2.5;PA + CA200:14.4±1.8;PA + FOs:15.2±2.4;PA + CA200 + FOs:11.9±1.5),FOs和CA共同协同降低了脂质蓄积。基因表达和免疫印迹分析证实了FOs和CA在上调AMPK介导的PPARα/UCP2以及下调AMPK介导的SREBP-1/FAS信号通路方面的联合作用。总体而言,这些结果表明将FOs与CA联合使用可作为NAFLD的一种潜在联合治疗方法。

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