Grape-seed derived procyanidins interfere with adipogenesis of 3T3-L1 cells at the onset of differentiation

Int J Obes (Lond). 2005 Aug;29(8):934-41. doi: 10.1038/sj.ijo.0802988.

Abstract

Objective: Our group's previous results on the effects of a grape seed procyanidin extract (GSPE) on adipose metabolism showed that peroxisome proliferator-activated receptor-gamma (PPARgamma) plays a central role in the lipolytic effects of GSPE on adipocytes. Since PPARgamma2 is a main regulator of the differentiation process of adipocytes, we investigated whether GSPE affects the adipogenesis of 3T3-L1 cells.

Design: We performed a time point screening by treating 3T3-L1 cells with GSPE during the differentiation process for 24 h.

Measurements: Differentiation markers and differential gene expression due to GSPE treatment (using the microarray technique).

Results: Twenty four hour-GSPE treatment at the onset of differentiation reduces adipose-specific markers and maintains the expression of preadipocyte marker preadipocyte factor-1 (Pref-1) significantly elevated. These effects were not found in other time points. Microarray analysis of gene expression after GSPE treatment at the early stage of differentiation showed a modified gene expression profile in which cell cycle and growth-related genes were downregulated by GSPE.

Conclusion: These results suggest that GSPE affects adipogenesis, mainly at the induction of differentiation, and that procyanidins may have a new role in which they impede the formation of adipose cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology*
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Animals
  • Antioxidants / pharmacology*
  • Base Sequence
  • Biflavonoids / pharmacology*
  • Biomarkers / analysis
  • Calcium-Binding Proteins
  • Catechin / pharmacology*
  • Cell Cycle Proteins / genetics
  • Cell Differentiation / drug effects
  • Gene Expression Regulation / drug effects
  • Glucosephosphate Dehydrogenase / genetics
  • Intercellular Signaling Peptides and Proteins
  • Lipids / analysis
  • Membrane Proteins / analysis
  • Membrane Proteins / genetics
  • Mice
  • Microarray Analysis
  • Molecular Sequence Data
  • PPAR gamma / analysis
  • PPAR gamma / genetics
  • Proanthocyanidins / pharmacology*
  • Repressor Proteins / analysis
  • Repressor Proteins / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Seeds
  • Triglycerides / analysis
  • Vitis*

Substances

  • Antioxidants
  • Biflavonoids
  • Biomarkers
  • Calcium-Binding Proteins
  • Cell Cycle Proteins
  • Dlk1 protein, mouse
  • Intercellular Signaling Peptides and Proteins
  • Lipids
  • Membrane Proteins
  • PPAR gamma
  • Proanthocyanidins
  • Repressor Proteins
  • Triglycerides
  • procyanidin
  • Catechin
  • Glucosephosphate Dehydrogenase