College of Pharmacy and Research Institute of Pharmaceutical Science, Seoul National University, Daehak-Dong, San 56-1, Sillim-Dong, Gwanak-Gu, Seoul 151-742, Republic of Korea.
Bioorg Med Chem Lett. 2013 Jun 1;23(11):3170-4. doi: 10.1016/j.bmcl.2013.04.011. Epub 2013 Apr 10.
Recently, obesity is a complex multifactorial chronic disease increasing the risk for type 2 diabetes, coronary heart disease and hypertension, and has become a major worldwide health problem. In the course of screening natural products employing 3T3-L1 cells as an in vitro system, the methanol extract of Idesia polycarpa Maxim. Fruits (Flacourtiaceae) significantly inhibited adipocyte differentiation by measuring lipid contents using oil red O staining. One new compound, 6-(oxymethyl)-2-hydroxyphenyl-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside (8), was isolated along with nine known compounds (1-7 and 9-10) from CHCl3 and n-BuOH fractions of the methanol extract of I. polycarpa fruits. Among them, idescarpin (1) with 1-hydroxy-6-oxo-2-cyclohexenecarboxylate moiety showed the most potent inhibitory activity on adipocyte differentiation with IC50 values of 23.2 μM. Idescarpin (1) dramatically suppressed the induction of C/EBPα expression, whereas it significantly increased the induction of PPARγ expression, supported by quantitative real time PCR and Western blot analysis. The down-regulation in mRNA levels of SREBP1c, SCD-1, and FAS by idescarpin (1) during adipocyte differentiation revealed that the inhibition of adipocyte differentiation was mediated by the regulation of lipogenesis. Taken together, we suggest that idescarpin (1) shows a great potential against obesity and diabetes though the anti-adipogenic activity and the up-regulation of PPARγ.
最近,肥胖是一种复杂的多因素慢性疾病,会增加 2 型糖尿病、冠心病和高血压的风险,已成为一个全球性的主要健康问题。在采用 3T3-L1 细胞作为体外系统筛选天然产物的过程中,发现茶梨果实(茶梨科)的甲醇提取物通过油红 O 染色测量脂质含量,可显著抑制脂肪细胞分化。从甲醇提取物的 CHCl3 和 n-BuOH 部分分离到一个新化合物 6-(羟甲基)-2-羟基苯-O-β-D-吡喃葡萄糖基-(1→6)-β-D-吡喃葡萄糖苷(8),以及 9 个已知化合物(1-7 和 9-10)。其中,具有 1-羟基-6-氧代-2-环己烯羧酸酯部分的茶梨素(1)对脂肪细胞分化的抑制活性最强,IC50 值为 23.2 μM。茶梨素(1)显著抑制 C/EBPα 的表达诱导,而通过定量实时 PCR 和 Western blot 分析,它显著增加了 PPARγ 的表达诱导。在脂肪细胞分化过程中,SREBP1c、SCD-1 和 FAS 的 mRNA 水平下调表明,脂肪细胞分化的抑制是通过脂生成的调节介导的。综上所述,我们认为茶梨素(1)通过抗脂肪生成活性和 PPARγ 的上调,显示出在肥胖和糖尿病方面的巨大潜力。