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田基黄通过激活 3T3-L1 细胞中的 AMP 激活的蛋白激酶发挥抗肥胖作用。

Anti-obesity effects of Boussingaulti gracilis Miers var. pseudobaselloides Bailey via activation of AMP-activated protein kinase in 3T3-L1 cells.

机构信息

Department of Hygienic Chemistry, College of Pharmacy, Kyung Hee University, Seoul, Korea.

出版信息

J Med Food. 2012 Sep;15(9):811-7. doi: 10.1089/jmf.2011.2126. Epub 2012 Aug 7.

Abstract

In a previous study, we demonstrated the anti-obesity and hypolipidemic effects of Boussingaulti gracilis Miers var. pseudobaselloides Bailey in high-fat diet-induced obese rats. The present study investigated the molecular mechanisms by which B. gracilis Miers var. pseudobaselloides Bailey ethanol extract (BGE) conferred antidifferentiation and anti-adipogenic effects in the 3T3-L1 preadipocyte differentiation model. BGE treatment significantly and dose-dependently suppressed lipid accumulation and down-regulated the expression of major transcription factors involved in adipogenesis, such as peroxisome proliferator-activated receptor-γ, CCAAT/enhancer binding protein α, sterol regulatory element-binding proteins, and their target genes. It is important that treatment with BGE increased phosphorylation of AMP-activated protein kinase (AMPK), which is one of the rate-limiting enzymes in the fatty acid synthesis pathway, and its direct downstream protein, acetyl-coenzyme A carboxylase. These results suggest that BGE may exert anti-adipogenic effects through regulation of AMPK activity and expression of genes involved in lipogenesis.

摘要

在之前的研究中,我们证明了美丽胡枝子 Bailey 变种假地蓝乙醇提取物(BGE)在高脂饮食诱导的肥胖大鼠中具有抗肥胖和降血脂作用。本研究探讨了 BGE 赋予 3T3-L1 前脂肪细胞分化模型抗分化和抗脂肪生成作用的分子机制。BGE 处理显著且呈剂量依赖性地抑制脂质积累,并下调参与脂肪生成的主要转录因子的表达,如过氧化物酶体增殖物激活受体-γ、CCAAT/增强子结合蛋白-α、固醇调节元件结合蛋白及其靶基因。重要的是,BGE 处理增加了 AMP 激活的蛋白激酶(AMPK)的磷酸化,AMPK 是脂肪酸合成途径中的限速酶之一,以及其直接下游蛋白乙酰辅酶 A 羧化酶。这些结果表明,BGE 可能通过调节 AMPK 活性和参与脂肪生成的基因表达发挥抗脂肪生成作用。

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