Nagatomo Akifumi, Nishida Norihisa, Matsuura Yoichi, Shibata Nobuhito
Research and Development Division, Morishita Jintan Co., Ltd., Osaka 573-0128, Japan ; Department of Biopharmaceutics, Faculty of Pharmaceutical Sciences, Doshisha Women's College of Liberal Arts, Kyoto 610-0395, Japan.
Research and Development Division, Morishita Jintan Co., Ltd., Osaka 573-0128, Japan.
Prev Nutr Food Sci. 2013 Jun;18(2):85-91. doi: 10.3746/pnf.2013.18.2.085.
Recent studies have shown that Rosa canina L. and tiliroside, the principal constituent of its seeds, exhibit anti-obesity and anti-diabetic activities via enhancement of fatty acid oxidation in the liver and skeletal muscle. However, the effects of rosehip, the fruit of this plant, extract (RHE), or tiliroside on lipid accumulation in adipocytes have not been analyzed. We investigated the effects of RHE and tiliroside on lipid accumulation and protein expression of key transcription factors in both in vitro and in vivo models. RHE and tiliroside inhibited lipid accumulation in a dose-dependent manner in 3T3-L1 cells. We also analyzed the inhibitory effect of RHE on white adipose tissue (WAT) in high-fat diet (HFD)-induced obesity mice model. Male C57BL/6J mice were fed HFD or HFD supplemented with 1% RHE (HFDRH) for 8 weeks. The HFDRH-fed group gained less body weight and had less visceral fat than the HFD-fed group. Liver weight was significantly lower in the HFDRH-fed group and total hepatic lipid and triglyceride (TG) content was also reduced. A significant reduction in the expression of peroxisome proliferator-activated receptor gamma (PPARγ) was observed in epididymal fat in the HFDRH-fed group, in comparison with controls, through Western blotting. These results suggest that downregulation of PPARγ expression is involved, at least in part, in the suppressive effect of RHE on lipid accumulation in WAT.
最近的研究表明,犬蔷薇及其种子的主要成分椴树苷,通过增强肝脏和骨骼肌中的脂肪酸氧化,表现出抗肥胖和抗糖尿病活性。然而,该植物果实玫瑰果提取物(RHE)或椴树苷对脂肪细胞脂质积累的影响尚未得到分析。我们在体外和体内模型中研究了RHE和椴树苷对脂质积累以及关键转录因子蛋白表达的影响。RHE和椴树苷在3T3-L1细胞中以剂量依赖性方式抑制脂质积累。我们还分析了RHE对高脂饮食(HFD)诱导的肥胖小鼠模型中白色脂肪组织(WAT)的抑制作用。雄性C57BL/6J小鼠喂食HFD或补充1%RHE的HFD(HFDRH)8周。与喂食HFD的组相比,喂食HFDRH的组体重增加较少,内脏脂肪也较少。喂食HFDRH的组肝脏重量显著降低,肝脏总脂质和甘油三酯(TG)含量也降低。通过蛋白质印迹法观察到,与对照组相比,喂食HFDRH的组附睾脂肪中过氧化物酶体增殖物激活受体γ(PPARγ)的表达显著降低。这些结果表明,PPARγ表达的下调至少部分参与了RHE对WAT中脂质积累的抑制作用。