Modulation of adipogenesis, lipolysis and glucose consumption in 3T3-L1 adipocytes and C2C12 myotubes by hydroxytyrosol acetate: a comparative study

Biochem Biophys Res Commun. 2013 Nov 1;440(4):576-81. doi: 10.1016/j.bbrc.2013.09.106. Epub 2013 Oct 4.

Abstract

Hydroxytyrosol acetate (Hd-Ac) is a polyphenol that is present in the olive fruit and oil at a concentration similar to that of hydroxytyrosol (Hd). The effects of Hd-Ac on adipogenesis, lipolysis, and glucose consumption in 3T3-L1 cells were investigated. Treatment with Hd-Ac at concentrations of 0-75 μmol/L inhibited 3T3-L1 differentiation and lipid accumulation in a dose-dependent manner. At the same concentration range, no effect on cell viability was observed in the MTT assay. Inhibition of adipogenesis was associated with the downregulation of PPARγ, C/EBPα, SREBP-1c, and their downstream target genes (GLUT4, CD36, and FAS) as revealed by qRT-PCR. On the other hand, Hd-Ac dose dependently activated glycerol release in fully differentiated 3T3-L1 adipocytes, indicating lipolysis. This stimulation of lipolysis was mediated via the activation of hormone-sensitive lipase (HSL) by phosphorylation at Ser563 and Ser660, and the phosphorylation of perilipin. Further investigation of the in vitro activities of this polyphenol showed that Hd-Ac has the capability to increase glucose consumption in 3T3-L1 adipocytes and C2C12 myotubes.

Keywords: C/EBPα; HSL; Hydroxytyrosol acetate; PPARγ; Perilipin; SREBP-1c.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Adipogenesis / drug effects*
  • Adipogenesis / genetics
  • Animals
  • CD36 Antigens / genetics
  • Gene Expression / drug effects
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / genetics
  • Imidazoles / pharmacology
  • Lipolysis / drug effects*
  • Mice
  • Muscle Fibers, Skeletal / drug effects*
  • Muscle Fibers, Skeletal / metabolism
  • Polyphenols / pharmacology*
  • Sulfhydryl Compounds / pharmacology
  • Transcription Factors / antagonists & inhibitors
  • fas Receptor / genetics

Substances

  • CD36 Antigens
  • Fas protein, mouse
  • Glucose Transporter Type 4
  • Imidazoles
  • N-dodecyl-2-mercaptoimidazole
  • Polyphenols
  • Sulfhydryl Compounds
  • Transcription Factors
  • fas Receptor
  • Glucose