首页> 美国卫生研究院文献>Nutrients >Dihydropyranocoumarins Exerted Anti-Obesity Activity In Vivo and its Activity Was Enhanced by Nanoparticulation with Polylactic-Co-Glycolic Acid
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Dihydropyranocoumarins Exerted Anti-Obesity Activity In Vivo and its Activity Was Enhanced by Nanoparticulation with Polylactic-Co-Glycolic Acid

机译:二氢吡喃香豆素体内具有抗肥胖作用并且通过聚乳酸-共-乙醇酸的纳米颗粒作用增强了它的活性

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摘要

Dihydropyranocoumarins (DPCs) were isolated from Thunb as anti-obesity compounds in 3T3-L1 adipocytes assay; however, it is uncertain whether DPC exerts anti-obesity activity in vivo. Therefore, this study evaluated the oral intake of pure DPCs in mice fed a high-fat diet, and also attempted to enhance its activity by nanoparticulation. Increases in body weight gain and fat accumulation in white adipose tissues were significantly suppressed by the dietary intake of DPCs (1.943 mg/mouse/day). DPCs intake also significantly decreased the mean size of adipocytes and upregulated mRNA levels of thermogenesis-related genes. Nanoparticulation of DPCs with polylactic-co-glycolic acid (PLGA) dramatically increased its activity almost 100-fold over that of a non-nanoparticulated form. Thus, our findings clearly demonstrated the anti-obesity activity of DPCs in vivo and suggested that PLGA nanoparticle encapsulation was useful to enhance the anti-obesity activity of DPCs with the aim to develop natural and safe anti-obesity agents.
机译:从Thunb中分离出二氢吡喃香豆素(DPC)作为抗肥胖化合物,用于3T3-L1脂肪细胞测定;但是,尚不确定DPC是否在体内发挥抗肥胖作用。因此,本研究评估了高脂饮食喂养的小鼠口服纯DPC的摄入量,并试图通过纳米颗粒增强其活性。 DPCs的饮食摄入量(1.943 mg /小鼠/天)显着抑制了白色脂肪组织中体重增加和脂肪积累的增加。 DPC的摄入还显着降低了脂肪细胞的平均大小,并与生热相关基因的mRNA水平上调。含聚乳酸-乙醇酸(PLGA)的DPC的纳米微粒化使其活性几乎比非纳米微粒形式的活性高100倍。因此,我们的发现清楚地证明了DPC的体内抗肥胖活性,并提示PLGA纳米颗粒封装可用于增强DPC的抗肥胖活性,目的是开发天然安全的抗肥胖剂。

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