Research Institute for Biological Functions, Chubu University, 1200 Matsumoto, Kasugai, Aichi, 487-8501, Japan.
Cytotechnology. 2010 Aug;62(4):367-76. doi: 10.1007/s10616-010-9288-7. Epub 2010 Sep 23.
The present study examined the anti-obesity effect and mechanism of action of Korean white ginseng extracts (KGE) using high-fat diet (HFD)-induced obese mice. Mice were fed a low-fat diet (LFD), HFD or HFD containing 0.8 and 1.6% (w/w) KGE diet (HFD + 0.8KGE and HFD + 1.6KGE) for 8 weeks. We also examined the effects of KGE on plasma triglyceride (TG) elevation in mice administrated with oral lipid emulsion. Body weight gain and white adipose tissue (WAT) weight were significantly decreased in the HFD + 1.6KGE group, compared with the HFD group. The plasma TG levels were also significantly reduced in both HFD + 0.8KGE and HFD + 1.6KGE groups, while leptin levels were significantly decreased in only the HFD + 1.6KGE group, compared with the HFD group. The HFD + 1.6KGE group showed significantly lower mRNA levels of lipogenesis-related genes, including peroxisome proliferator-activated receptorγ2 (PPARγ2), sterol regulatory element binding protein-1c (SREBP-1c), lipoprotein lipase (LPL), fatty acid synthase (FAS) and diacylglycerol acyltransferase 1 (DGAT1), compared with the HFD group. In addition, a dose of 1000 mg/kg KGE inhibited the elevation of plasma TG levels compared with mice given the lipid emulsion alone. These results suggest that the anti-obesity effects of KGE may be elicited by regulating expression of lipogenesis-related genes in WAT and by delaying intestinal fat absorption.
本研究采用高脂饮食(HFD)诱导肥胖小鼠,考察高丽白参提取物(KGE)的抗肥胖作用及其作用机制。小鼠分别喂食低脂饮食(LFD)、HFD 或含 0.8%和 1.6%(w/w)KGE 的 HFD 饮食(HFD+0.8KGE 和 HFD+1.6KGE)8 周。我们还考察了 KGE 对给予口服脂质乳剂的小鼠血浆甘油三酯(TG)升高的影响。与 HFD 组相比,HFD+1.6KGE 组的体重增加和白色脂肪组织(WAT)重量显著减少。HFD+0.8KGE 和 HFD+1.6KGE 组的血浆 TG 水平也显著降低,而仅 HFD+1.6KGE 组的瘦素水平显著降低。与 HFD 组相比,HFD+1.6KGE 组脂肪生成相关基因的 mRNA 水平显著降低,包括过氧化物酶体增殖物激活受体γ2(PPARγ2)、固醇调节元件结合蛋白-1c(SREBP-1c)、脂蛋白脂肪酶(LPL)、脂肪酸合酶(FAS)和二酰基甘油酰基转移酶 1(DGAT1)。此外,与单独给予脂质乳剂的小鼠相比,1000mg/kg KGE 剂量可抑制血浆 TG 水平升高。这些结果表明,KGE 的抗肥胖作用可能是通过调节 WAT 中脂肪生成相关基因的表达和延缓肠道脂肪吸收来实现的。