Anti-obesity effects of Lysimachia foenum-graecum characterized by decreased adipogenesis and regulated lipid metabolism

被引:50
|
作者
Seo, Jong Bae [1 ]
Choe, Sung Sik [1 ]
Jeong, Hyun Woo [2 ]
Park, Sang Wook [1 ]
Shin, Hyun Jung [2 ]
Choi, Sun Mi [1 ]
Park, Jae Young [1 ]
Choi, Eun Wook [1 ]
Kim, Jae Bum [2 ,3 ]
Seen, Dong Seung [1 ]
Jeong, Jae-Yeon [1 ]
Lee, Tae Gyu [1 ]
机构
[1] Seoul Natl Univ, BRN Sci Co Ltd, R&D Ctr, Biotechnol Incubating Ctr, Seoul 151742, South Korea
[2] Seoul Natl Univ, Sch Biol Sci, Inst Mol Biol & Genet, Seoul 151742, South Korea
[3] Seoul Natl Univ, Dept Biophys & Chem Biol, Seoul 151742, South Korea
来源
EXPERIMENTAL AND MOLECULAR MEDICINE | 2011年 / 43卷 / 04期
关键词
adipocyte differentiation; fatty acid oxidation; fatty acid synthesis; lipid metabolism; Lysimachia foenum-graecum; obesity; ACTIVATED PROTEIN-KINASE; REVERSES INSULIN-RESISTANCE; VISCERAL ADIPOSE-TISSUE; FATTY-ACID OXIDATION; ADIPOCYTE DIFFERENTIATION; PPAR-GAMMA; HORMONE ADIPONECTIN; SKELETAL-MUSCLE; OBESITY; PHOSPHORYLATION;
D O I
10.3858/emm.2011.43.4.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lysimachia foenum-graecum has been used as an oriental medicine with anti-inflammatory effect. The anti-obesity effect of L. foenum-graecum extract (LFE) was first discovered in our screening of natural product extract library against adipogenesis. To characterize its anti-obesity effects and to evaluate its potential as an anti-obesity drug, we performed various obesity-related experiments in vitro and in vivo. In adipogenesis assay, LFE blocked the differentiation of 3T3-L1 preadipocyte in a dose-dependent manner with an IC50 of 2.5 mu g/ml. In addition, LFE suppressed the expression of lipogenic genes, while increasing the expression of lipolytic genes in vitro at 10 mu g/ml and in vivo at 100 mg/kg/day. The anti-adipogenic and anti-lipogenic effect of LFE seems to be mediated by the inhibition of PPAR gamma and C/EBP alpha expression as shown in in vitro and in vivo, and the suppression of PPAR gamma activity in vitro. Moreover, LFE stimulated fatty acid oxidation in an AMPK-dependent manner. In high-fat diet (HFD)-induced obese mice (n = 8/group), oral administration of LFE at 30, 100, and 300 mg/kg/day decreased total body weight gain significantly in all doses tested. No difference in food intake was observed between vehicle- and LFE-treated HFD mice. The weight of white adipose tissues including abdominal subcutaneous, epididymal, and perirenal adipose tissue was reduced markedly in LFE-treated HFD mice in a dose-dependent manner. Treatment of LFE also greatly improved serum levels of obesity-related biomarkers such as glucose, triglycerides, and adipocytokines leptin, adiponectin, and resistin. All together, these results showed anti-obesity effects of LFE on adipogenesis and lipid metabolism in vitro and in vivo and raised a possibility of developing LFE as anti-obesity therapeutics.
引用
收藏
页码:205 / 215
页数:11
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