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Bioassay-guided isolation of active anti-adipogenic compound from royal jelly and the study of possible mechanisms

机译:生物测定指导的蜂王浆中活性抗脂肪形成化合物的分离及其可能机理的研究

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Royal jelly (RJ) has been used traditionally for dietary, cosmetic and health purposes for a long time in different parts of the world. Scientific studies have also shown its numerous health-promoting properties including hypoglycemic and anti-hypercholesterolemic action. In this study, we investigated the anti-adipogenic activity of RJ in 3?T3-L1 cells and isolated the major responsible root component for the activity. An active anti-adipogenic compound was isolated through bioassay-guided isolation process by successive treatment of RJ and its active fractions on 3?T3-L1 cell line. (E)-10-Hydroxy-2-decenoic Acid (10-HDA) was identified using NMR spectroscopy and ultra-performance liquid chromatography (UPLC). As 10-HDA showed significant anti-adipogenic activity with Oil Red O staining and TG content assay on 3?T3-L1 adipocytes, further study was carried out in molecular level for the expression of adipogenic transcription factors such as PPARγ, FABP4, C/EBPα, SREBP-1c, and Leptin. The effect of 10-HDA on preliminary molecules such as pAkt, pERK, C/EBPβ, and pCREB were studied in the early stage of adipogenesis. The effect of 10-HDA on reactive oxygen species (ROS) production in fully differentiating adipocytes was measured by nitro blue tetrazolium (NBT) assay. Results showed that triacylglycerol accumulation and ROS production was markedly suppressed by 10-HDA. Preliminary molecules such as pAkt, pERK, pCERB, and C/EBPβ were found to be down-regulated by 10-HDA, which led to down-regulation of key adipogenic transcription factors such as PPARγ, FABP4, CEBPα, SREBP-1c, and Leptin on 3?T3-L1 adipocytes. Our results suggest that anti-adipogenesis of 10-HDA on 3?T3-L1 adipocyte takes place via two mechanisms: inhibition of cAMP/PKA pathway and inhibition of p-Akt and MAPK dependent insulin signaling pathway. So it is considered that 10-HDA, a major component of RJ, can be a potential therapeutic medicine for obesity.
机译:蜂王浆(RJ)在世界各地长期以来一直被用于饮食,化妆品和健康用途。科学研究还显示了其众多的健康促进特性,包括降血糖和抗高胆固醇血症作用。在这项研究中,我们调查了RJ在3?T3-L1细胞中的抗脂肪形成活性,并分离了该活性的主要负责根成分。通过在3?T3-L1细胞系中连续处理RJ及其活性级分,通过生物测定指导的分离过程分离出活性抗脂肪形成化合物。 (E)-10-羟基-2-癸烯酸(10-HDA)使用NMR光谱法和超高效液相色谱法(UPLC)鉴定。由于10-HDA在3?T3-L1脂肪细胞上经油红O染色和TG含量测定显示出显着的抗脂肪形成活性,因此在分子水平上进一步研究了脂肪形成转录因子(如PPARγ,FABP4,C / EBPα,SREBP-1c和Leptin。在脂肪形成的早期阶段,研究了10-HDA对初步分子如pAkt,pERK,C /EBPβ和pCREB的影响。 10-HDA对完全分化的脂肪细胞中活性氧(ROS)产生的影响通过硝基蓝四唑(NBT)测定来测量。结果表明,10-HDA显着抑制了三酰甘油的积累和ROS的产生。发现初步分子(例如pAkt,pERK,pCERB和C /EBPβ)受到10-HDA的下调,从而导致关键的成脂转录因子(如PPARγ,FABP4,CEBPα,SREBP-1c和PPARγ)下调。瘦素在3?T3-L1脂肪细胞上。我们的结果表明10-HDA在3?T3-L1脂肪细胞上的抗脂肪形成通过两种机制发生:抑制cAMP / PKA途径和抑制p-Akt和MAPK依赖性胰岛素信号传导途径。因此,人们认为RJ的主要成分10-HDA可能是肥胖的潜在治疗药物。

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