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酶处理的海带提取物通过下调3T3-L1脂肪细胞中的C/EBPα来抑制脂肪生成。

Enzyme-treated Ecklonia cava extract inhibits adipogenesis through the downregulation of C/EBPα in 3T3-L1 adipocytes.

作者信息

Kim In-Hye, Nam Taek-Jeong

机构信息

Institute of Fisheries Science, Pukyong National University, Busan 619-911, Republic of Korea.

出版信息

Int J Mol Med. 2017 Mar;39(3):636-644. doi: 10.3892/ijmm.2017.2869. Epub 2017 Jan 26.

Abstract

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.

摘要

在本研究中,我们检测了酶处理的海蕴(EEc)提取物对3T3-L1脂肪细胞脂肪生成的抑制作用。首先使用消化酶果胶酶(Rapidase® X-Press L)和纤维素酶(Rohament® CL)对海蕴(E. cava)的成分进行分离和纯化。我们发现EEc提取物含有三种不同的间苯三酚单宁:eckol、dieckol和phlorofucofuroeckol-A。在这些间苯三酚单宁中,dieckol在EEc提取物中含量最高,为16 mg/g。然后,我们使用3T3-L1脂肪细胞在体外检测了EEc提取物处理对分化相关转录因子和脂肪生成相关基因表达的抑制作用。使用3T3-L1前脂肪细胞来确定不会导致细胞毒性的EEc提取物和藤黄果(Gar)提取物的浓度。50 μg/ml的EEc和200 μg/ml的Gar对EEc处理的脂肪细胞中的葡萄糖利用和甘油三酯(TG)积累有类似的抑制作用,这些结果通过油红O染色得到证实。我们还检测了EEc提取物处理后脂肪生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。EEc提取物处理降低了脂肪生成相关基因的表达水平,特别是固醇调节元件结合蛋白-1c(SREBP-1c)、脂肪细胞脂肪酸结合蛋白(A-FABP)、脂肪酸合酶(FAS)和脂联素。这些结果表明,EEc提取物处理对脂肪生成有抑制作用,具体是通过影响C/EBPα信号通路的激活以及由此产生的脂肪生成相关基因表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a767/5360387/033c5de035c1/IJMM-39-03-0636-g00.jpg

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