Anti-adipogenic activity of compounds isolated from Idesia polycarpa on 3T3-L1 cells

Bioorg Med Chem Lett. 2013 Jun 1;23(11):3170-4. doi: 10.1016/j.bmcl.2013.04.011. Epub 2013 Apr 10.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipogenesis / drug effects
  • Animals
  • Anti-Obesity Agents / chemistry*
  • Anti-Obesity Agents / isolation & purification
  • Anti-Obesity Agents / pharmacology
  • CCAAT-Enhancer-Binding Protein-alpha / genetics
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism
  • Cyclohexanecarboxylic Acids / chemistry*
  • Cyclohexanecarboxylic Acids / isolation & purification
  • Cyclohexanecarboxylic Acids / pharmacology
  • Disaccharides / chemistry*
  • Disaccharides / isolation & purification
  • Disaccharides / pharmacology
  • Down-Regulation / drug effects
  • Fruit / chemistry
  • Glucosides / chemistry*
  • Glucosides / isolation & purification
  • Glucosides / pharmacology
  • Magnetic Resonance Spectroscopy
  • Mice
  • Molecular Conformation
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • RNA, Messenger / metabolism
  • Salicaceae / chemistry*
  • Stearoyl-CoA Desaturase / genetics
  • Stearoyl-CoA Desaturase / metabolism
  • Sterol Regulatory Element Binding Protein 1 / genetics
  • Sterol Regulatory Element Binding Protein 1 / metabolism
  • fas Receptor / genetics
  • fas Receptor / metabolism

Substances

  • Anti-Obesity Agents
  • CCAAT-Enhancer-Binding Protein-alpha
  • Cyclohexanecarboxylic Acids
  • Disaccharides
  • Fas protein, mouse
  • Glucosides
  • PPAR gamma
  • RNA, Messenger
  • Sterol Regulatory Element Binding Protein 1
  • fas Receptor
  • idescarpin
  • Scd1 protein, mouse
  • Stearoyl-CoA Desaturase