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Nobiletin Suppresses Adipogenesis by Regulating the Expression of Adipogenic Transcription Factors and the Activation of AMP-Activated Protein Kinase (AMPK)

机译:Nobiletin通过调节成脂转录因子的表达和AMP激活的蛋白激酶(AMPK)的激活来抑制脂肪生成。

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The objective of this study was to elucidate the effect of nobiletin (5,6,7,8,3',4'-hexamethoxyflavone) on adipogenesis in 3T3-L1 cells. To determine the effect of nobiletin on adipogenesis, preadipocyte differentiation was induced in the presence or absence of nobiletin (10—100 μM) for 4 days. The results revealed that nobiletin markedly inhibited lipid accumulation and glycerol-3-phosphate dehydrogenase (GPDH) activity and blocked the expression of adipogenic transcription factors, including peroxisome proliferator-activated receptors (PPARy) and CCAAT/enhancer binding proteins (C/EBPα). Moreover, nobiletin signincandy increased AMP-activated protein kinase (AMPK), a major regulator of cellular energy balance, phosphorylation, and intracellular reactive oxygen species (ROS) generation. This study also investigated the involvement of AMPK in the expression of a major transcription factor, PPARy, It was found that pretreatment with compound C, a cell permeable inhibitor of AMPK, abolished the inhibitory effects of nobiletin on PPARy expression. The results suggest that nobiletin exerts antiadipogenic effects through modulation of the PPARy and AMPK signaling pathway and, therefore, may be a promising antiobesity agent.
机译:这项研究的目的是阐明Nobiletin(5,6,7,8,3',4'-六甲氧基黄酮)对3T3-L1细胞脂肪形成的影响。为了确定Nobiletin对脂肪生成的影响,在存在或不存在Nobiletin(10-100μM)的情况下,诱导脂肪细胞前分化4天。结果显示,诺比列汀显着抑制脂质积累和3-磷酸甘油脱氢酶(GPDH)活性,并阻断包括过氧化物酶体增殖物激活受体(PPARy)和CCAAT /增强子结合蛋白(C /EBPα)在内的成脂转录因子的表达。而且,诺比列汀明显增加了AMP激活的蛋白激酶(AMPK),AMPK是细胞能量平衡,磷酸化和细胞内活性氧(ROS)生成的主要调节剂。这项研究还研究了AMPK在主要转录因子PPARy表达中的参与。发现用化合物C(AMPK的细胞可渗透抑制剂)进行的预处理消除了Nobiletin对PPARy表达的抑制作用。结果表明,诺比列汀通过调节PPARy和AMPK信号通路发挥抗脂肪形成作用,因此可能是有前途的抗肥胖药。

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