Saponins from Platycodon grandiflorum inhibit hepatic lipogenesis through induction of SIRT1 and activation of AMP-activated protein kinase in high-glucose-induced HepG2 cells

Food Chem. 2013 Sep 1;140(1-2):115-23. doi: 10.1016/j.foodchem.2013.02.041. Epub 2013 Feb 21.

Abstract

Saponins from the roots of Platycodon grandiflorum (Changkil saponins, CKS) have antioxidant and hepatoprotective properties. This study investigated the effects of CKS on AMP-activated protein kinase (AMPK) activation and hepatic lipogenesis in HepG2 cells. CKS suppressed high-glucose-induced lipid accumulation and inhibited high-glucose-induced fatty acid synthase (FAS) and sterol regulatory element binding protein-1c (SREBP-1c) expression in HepG2 cells. Moreover, the use of a pharmacological AMPK inhibitor revealed that AMPK is essential for the suppression of SREBP-1c expression in CKS-treated cells. Finally, the activation of calcium/calmodulin-dependent kinase kinase β (CaMKKβ) and SIRT1 was necessary for CKS-enhanced activation of AMPK. These results indicate that CKS prevents lipid accumulation in HepG2 cells by blocking the expression of SREBP-1c and FAS through SIRT1 and CaMKKβ/AMPK activation. Using CKS to target AMPK activation may provide a promising approach for the prevention lipogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism*
  • Down-Regulation / drug effects*
  • Enzyme Activation / drug effects
  • Glucose / metabolism*
  • Hep G2 Cells
  • Humans
  • Lipid Metabolism / drug effects
  • Lipogenesis / drug effects*
  • Liver / drug effects
  • Liver / metabolism*
  • Phosphorylation / drug effects
  • Plant Extracts / pharmacology*
  • Platycodon / chemistry*
  • Saponins / pharmacology*
  • Sirtuin 1 / genetics*
  • Sirtuin 1 / metabolism
  • fas Receptor / genetics
  • fas Receptor / metabolism

Substances

  • FAS protein, human
  • Plant Extracts
  • Saponins
  • fas Receptor
  • AMP-Activated Protein Kinases
  • SIRT1 protein, human
  • Sirtuin 1
  • Glucose