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首页> 外文期刊>International journal of molecular medicine >Enzyme-treated Ecklonia cava extract inhibits adipogenesis through the downregulation of C/EBPα in 3T3-L1 adipocytes
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Enzyme-treated Ecklonia cava extract inhibits adipogenesis through the downregulation of C/EBPα in 3T3-L1 adipocytes

机译:酶处理的Ecklonia cava提取物通过下调3T3-L1脂肪细胞中C /EBPα来抑制脂肪形成

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摘要

In this study, we examined the inhibitory effects of enzyme- treated Ecklonia cava (EEc) extract on the adipogenesis of 3T3-L1 adipocytes. The components of Ecklonia cava (E.?cava) were first separated and purified using the digestive enzymes pectinase (Rapidase??X?Press L) and cellulase (Rohament??CL). We found that the EEc extract contained three distinct phlorotannins: eckol, dieckol and phlorofucofuroeckol-A. Among the phlorotannins, dieckol was the most abundant in the EEc extract at 16?mg/g. Then we examined the inhibitory effects of EEc extract treatment on differentiation?related transcription factors and on adipogenesis?related gene expression in?vitro using 3T3-L1 adipocytes. 3T3?L1 pre?adipocytes were used to determine the concentrations of the EEc extract and Garcinia cambogia (Gar) extract that did not result in cytotoxicity. Glucose utilization and triglyceride?(TG) accumulation in the EEc?treated adipocytes were similarly inhibited by 50?μg/ml EEc and 200?μg/ml Gar, and these results were confirmed by Oil Red?O?staining. Protein expression of adipogenesis differentiation?related transcription factors following treatment with the EEc extract was also examined. Only the expression of CCAAT/enhancer?binding protein (C/EBP)α was decreased, while there was no effect on the expression of C/EBPβ, C/EBPδ, and peroxisome proliferator?activated receptor?γ (PPARγ). Treatment with the EEc extract decreased the expression levels of adipogenesis?related genes, in particular sterol regulatory element binding protein?1c (SREBP?1c), adipocyte fatty acid binding protein (A?FABP), fatty acid synthase (FAS) and adiponectin. These results suggest that EEc extract treatment has an inhibitory effect on adipogenesis, specifically by affecting the activation of the C/EBPα signaling pathway and the resulting adipogenesis-related gene expression.
机译:在这项研究中,我们检查了酶处理的Ecklonia cava(EEc)提取物对3T3-L1脂肪细胞脂肪形成的抑制作用。首先用消化酶果胶酶(Rapidase→X→Press L)和纤维素酶(Rohament→CL)分离和纯化Ecklonia cava(大肠杆菌)的成分。我们发现EEc提取物包含三种不同的phrotrotannins:eckol,dieckol和phofofucofuroeckol-A。在邻苯二酚单宁中,二乙酚在EEc提取物中含量最高,为16?mg / g。然后,我们使用3T3-L1脂肪细胞研究了EEc提取物处理对体外分化相关转录因子和脂肪形成相关基因表达的抑制作用。使用3T3?L1前脂肪细胞确定未引起细胞毒性的EEc提取物和藤黄果提取物的浓度。 50?μg/ ml EEc和200?μg/ ml Gar相似地抑制了EEc?处理的脂肪细胞中的葡萄糖利用和甘油三酸酯(TG)的积累,并且油红?O?染色证实了这些结果。还检查了EEc提取物处理后脂肪形成分化相关转录因子的蛋白表达。仅CCAAT /增强子结合蛋白(C / EBP)α的表达降低,而对C /EBPβ,C /EBPδ和过氧化物酶体增殖物激活受体γ(PPARγ)的表达没有影响。用EEc提取物处理可降低脂肪形成相关基因的表达水平,特别是固醇调节元件结合蛋白α1c(SREBPβ1c),脂肪细胞脂肪酸结合蛋白(AβFABP),脂肪酸合酶(FAS)和脂联素。这些结果表明,EEc提取物处理对脂肪形成具有抑制作用,特别是通过影响C /EBPα信号通路的激活以及由此产生的与脂肪形成相关的基因表达。

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