Vitisin A inhibits adipocyte differentiation through cell cycle arrest in 3T3-L1 cells

Biochem Biophys Res Commun. 2008 Jul 18;372(1):108-13. doi: 10.1016/j.bbrc.2008.04.188. Epub 2008 May 13.

Abstract

Inhibition of adipocyte differentiation is one approach among the anti-obesity strategies. This study demonstrates that vitisin A, a resveratrol tetramer, inhibits adipocyte differentiation most effectively of 18 stilbenes tested. Fat accumulation and PPARgamma expression were decreased by vitisin A in a dose-dependent manner. Vitisin A significantly inhibited preadipocyte proliferation and consequent differentiation within the first 2 days of treatment, indicating that the anti-adipogenic effect of vitisin A was derived from anti-proliferation. Based on cell cycle analysis, vitisin A blocked the cell cycle at the G1-S phase transition, causing cells to remain in the preadipocyte state. Vitisin A increased p21 expression, while the Rb phosphorylation level was reduced. Therefore, vitisin A seems to induce G1 arrest through p21- and consequent Rb-dependent suppression of transcription. On the other hand, ERK and Akt signaling pathways were not involved in the anti-mitotic regulation by vitisin A. Taken together, these results suggest that vitisin A inhibits adipocyte differentiation through preadipocyte cell cycle arrest.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects*
  • Adipogenesis / drug effects*
  • Animals
  • Anti-Obesity Agents / pharmacology*
  • Benzofurans / pharmacology*
  • Cell Proliferation / drug effects
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Mice
  • Mitosis / drug effects*
  • PPAR gamma / antagonists & inhibitors
  • Phenols / pharmacology*
  • Phosphorylation / drug effects
  • Retinoblastoma Protein / metabolism
  • Signal Transduction / drug effects
  • Stilbenes / pharmacology*
  • Transcription, Genetic / drug effects

Substances

  • Anti-Obesity Agents
  • Benzofurans
  • Cyclin-Dependent Kinase Inhibitor p21
  • PPAR gamma
  • Phenols
  • Retinoblastoma Protein
  • Stilbenes
  • vitisin A