首页> 外文期刊>Journal of Experimental Pharmacology >Bioactive fraction from Lagerstroemia speciosa leaves (DLBS3733) reduces fat droplet by inhibiting adipogenesis and lipogenesis
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Bioactive fraction from Lagerstroemia speciosa leaves (DLBS3733) reduces fat droplet by inhibiting adipogenesis and lipogenesis

机译:紫薇叶子(DLBS3733)的生物活性成分通过抑制脂肪生成和脂肪生成减少脂肪滴

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Background: Obesity has become a risk factor for metabolic diseases. One of the cellular characteristics of obesity is the occurrence of adipose cells hyperplasia. Lagerstroemia speciosa is a plant which has been used for the treatment of diabetes. Furthermore, some studies also indicated that L. speciosa possesses antiobesity activity. Its antiobesity activity was examined in the present study through adipogenesis, lipogenesis, and lipolysis pathways. Aim: DLBS3733, a bioactive fraction of L. speciosa , was explored for its potential benefits to alter obesity through adipogenesis and lipogenesis inhibition and lipolysis induction activity. Materials and methods: This study was performed using 3T3-L1 cells. mRNA level and protein expressions related to adipogenesis, lipogenesis, and lipolysis pathways were assayed in this study. Results: Antiadipogenic effects of DLBS3733 (15 μg/mL) were found to be mediated by a significant downregulation of mRNA level of multicomponents involved in adipogenesis which include C/EBPα (CCAAT/enhancer-binding protein alpha) and PPAR-γ (peroxisome proliferator-activated receptor gamma) by 75% and 80.1% ( p 0.05), respectively. DLBS3733 was found to inhibit lipogenesis, as shown by the significant reductions of adiponectin excretion and mRNA level of fatty acid synthase, SREBP (sterol regulatory element-binding protein), and ACC-β (Acetyl-CoA carboxylase) by 44.7%, 70.9%, and 83.1%, respectively ( p 0.05). In addition, DLBS3733 was found to inhibit fat droplets accumulation in the cells in a dose-dependent manner through Oil-Red O staining. pAMPK protein was upregulated by 75% and ACC-β was downregulated by 88% ( p 0.05) which indicates the reduction of lipid synthesis. Meanwhile, DLBS3733 showed an insignificant effect on adipose triglyceride lipase, hormone-sensitive lipase, and carnitine palmitoyl-CoA transferase-1 which indicate that DLBS3733 does not induce lipolysis. Conclusion: These results demonstrate the inhibitory activity of DLBS3733 on adipogenesis and lipogenesis. DLBS3733 may provide an effective and potential benefit in the prevention of obesity.
机译:背景:肥胖已成为代谢疾病的危险因素。肥胖的细胞特征之一是脂肪细胞增生的发生。紫薇是一种已经用于治疗糖尿病的植物。此外,一些研究还表明,L。speciosa具有抗肥胖活性。在本研究中,通过脂肪生成,脂肪生成和脂解途径检查了其抗肥胖活性。目的:研究了DLBS3733,一种L. speciosa的生物活性部分,它具有通过脂肪形成和脂肪生成抑制以及脂肪分解诱导活性改变肥胖的潜在益处。材料和方法:本研究使用3T3-L1细胞进行。在这项研究中测定了与脂肪形成,脂肪形成和脂解途径有关的mRNA水平和蛋白质表达。结果:发现DLBS3733(15μg/ mL)的抗脂肪形成作用是通过显着下调参与脂肪形成的多种成分的mRNA水平介导的,这些成分包括C /EBPα(CCAAT /增强子结合蛋白α)和PPAR-γ(过氧化物酶体增殖物)激活受体γ)分别降低了75%和80.1%(p <0.05)。发现DLBS3733抑制脂肪生成,如脂联素排泄和脂肪酸合酶,SREBP(固醇调节元件结合蛋白)和ACC-β(乙酰辅酶A羧化酶)的mRNA水平显着降低所表明的那样。和分别为83.1%(p <0.05)。此外,发现DLBS3733通过油红O染色以剂量依赖性方式抑制细胞中的脂肪滴积累。 pAMPK蛋白上调了75%,ACC-β下调了88%(p <0.05),表明脂质合成减少。同时,DLBS3733对脂肪甘油三酸酯脂肪酶,激素敏感性脂肪酶和肉碱棕榈酰-CoA转移酶-1的影响不明显,这表明DLBS3733不会诱导脂解。结论:这些结果证明了DLBS3733对脂肪生成和脂肪生成的抑制活性。 DLBS3733可能在预防肥胖症方面提供有效和潜在的益处。

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