首页> 外文期刊>Journal of medicinal food >A Combination of Korean Red Ginseng Extract and Glycyrrhiza glabra L. Extract Enhances Their Individual Anti-Obesity Properties in 3T3-L1 Adipocytes and C57BL/6J Obese Mice
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A Combination of Korean Red Ginseng Extract and Glycyrrhiza glabra L. Extract Enhances Their Individual Anti-Obesity Properties in 3T3-L1 Adipocytes and C57BL/6J Obese Mice

机译:韩国红人参提取物和甘草提取物的组合提取物在3T3-L1 adipocytes和C57BL / 6J肥胖小鼠中增强了它们的个体抗肥胖特性

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Anti-obesity activities of Korean red ginseng saponin fraction (RGS) and/or Glycyrrhiza glabra L. extract (GG) were investigated in 3T3-L1 adipocytes and high-fat diet-induced C57BL/6J obese mice. RGS and GG extracts were mixed at a mass ratio of 3:1 (SG31), 1:1 (SG11), or 1:3 (SG13). SG31 showed the highest anti-obesity activity among the three different mass ratios of RGS and GG extracts. SG31 showed higher inhibition efficiency on triglyceride (TG) accumulation than either single extract in 3T3-L1 adipocytes and without any cytotoxicity. It also decreases the expression of adipogenic and lipogenic genes such as C/EBPα and SREBP-1c (sterol regulatory element-binding protein 1c). In the obese induced mouse model, SG31 significantly reduced white adipose tissue weight and body weight, attenuated dyslipidemia, and decreased serum TG levels. In some indices, the activity of SG31 was even higher compared with Garcinia Cambogia water extract, a positive control. The possible mechanism by which SG31 causes the above results was by activating the AMP-activated protein kinase (AMPK) pathway and stimulating the secretion of adiponectin in adipose tissue to regulate energy metabolism balance, inhibit TG formation, and promote β-oxidation of fatty acids. Therefore, SG31 may have efficacy as an anti-obesity functional food or raw material if the results can be confirmed in human studies.
机译:在3T3-L1脂肪细胞和高脂饮食诱导的C57BL / 6J肥胖小鼠中研究了韩国红人参皂苷群(RGS)和/或Glycyrrhiza Glabra L.提取物(GG)的抗肥胖活动。将RGS和GG提取物以3:1(SG31),1:1(SG11)或1:3(SG13)的质量比混合。 SG31显示了RGS和GG提取物的三种不同质量比的最高抗肥胖活动。 SG31显示出比3T3-L1脂肪细胞的单一提取物的甘油三酯(TG)积聚较高的抑制效率,并且没有任何细胞毒性。它还降低了脂肪生成和富血生基因如C /EBPα和Srebp-1C(甾醇调节元素结合蛋白1c)的表达。在肥胖诱导的小鼠模型中,SG31显着降低了白色脂肪组织重量和体重,减弱了血脂血症,降低了血清TG水平。在某些指数中,与小西甘蓝水提取物相比,SG31的活性甚至更高,阳性对照。 SG31引起上述结果的可能机制是通过激活AMP活化的蛋白激酶(AMPK)途径并刺激脂肪组织中脂联素的分泌,以调节能量代谢平衡,抑制TG形成,促进脂肪酸的β-氧化。因此,如果结果可以在人类研究中确认,则SG31可能具有抗肥胖功能性食品或原料的功效。

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