Marine Bioprocess Research Center, Pukyong National University, Busan, Republic of Korea.
Chem Biol Interact. 2010 Jun 7;186(1):24-9. doi: 10.1016/j.cbi.2010.04.003. Epub 2010 Apr 10.
Dioxinodehydroeckol (DHE) isolated from Ecklonia cava, has previously been investigated for its inhibition of the differentiation of 3T3-L1 preadipocytes into adipocytes. Levels of lipid accumulation were measured, along with changes in the expression of genes and proteins associated with adipogenesis and lipolysis. Confluent 3T3-L1 preadipocytes in medium with or without different concentrations of DHE for 7 days were differentiated into adipocytes. Lipid accumulation was quantified by measuring direct triglyceride contents and Oil-Red O staining. The expression of genes and proteins associated with adipogenesis and lipolysis was measured using RT-PCR, quantitative real-time RT-PCR and Western blotting analysis. It was found that the presence of DHE significantly reduced lipid accumulation and down-regulated the expression of peroxisome proliferator-activated receptor-gamma (PPARgamma), sterol regulatory element-binding protein 1 (SREBP1) and CCAAT/enhancer-binding proteins (C/EBPalpha) in a dose-dependent manner. Moreover, DHE suppressed regulation of the adipocyte-specific gene promoters such as fatty acid binding protein (FABP4), fatty acid transport protein (FATP1), fatty acid synthase (FAS), lipoprotein lipase (LPL), acyl-CoA synthetase 1 (ACS1), leptin, perilipin and HSL compared to control adipocytes. The specific mechanism mediating the effects of DHE was confirmed by activation of phosphorylated AMP-activated protein kinase (pAMPK). Therefore, these results suggest that DHE exerts anti-adipogenic effect on adipocyte differentiation through the activation and modulation of the AMPK signaling pathway.
二酮去氢表雄甾酮(DHE)是从裙带菜中分离得到的,先前的研究表明它可以抑制 3T3-L1 前脂肪细胞向脂肪细胞的分化。本研究检测了脂肪细胞分化过程中脂滴积累水平的变化,以及与脂肪生成和脂肪分解相关的基因和蛋白表达的变化。将处于融合状态的 3T3-L1 前脂肪细胞在含有不同浓度 DHE 的培养基中培养 7 天,诱导其分化为脂肪细胞。通过直接测定甘油三酯含量和油红 O 染色来定量分析脂滴积累。采用 RT-PCR、实时定量 RT-PCR 和 Western blot 分析检测与脂肪生成和脂肪分解相关的基因和蛋白的表达。结果表明,DHE 的存在可显著减少脂滴积累,并呈浓度依赖性地下调过氧化物酶体增殖物激活受体-γ(PPARγ)、固醇调节元件结合蛋白 1(SREBP1)和 CCAAT/增强子结合蛋白(C/EBPα)的表达。此外,DHE 抑制了脂肪细胞特异性基因启动子的调控,如脂肪酸结合蛋白(FABP4)、脂肪酸转运蛋白(FATP1)、脂肪酸合成酶(FAS)、脂蛋白脂肪酶(LPL)、酰基辅酶 A 合成酶 1(ACS1)、瘦素、脂滴包被蛋白( perilipin)和激素敏感脂肪酶(HSL)的表达,与对照脂肪细胞相比。通过激活磷酸化 AMP 激活蛋白激酶(pAMPK)证实了介导 DHE 作用的特定机制。因此,这些结果表明 DHE 通过激活和调节 AMPK 信号通路对脂肪细胞分化发挥抗脂肪生成作用。