Promotion of adiponectin multimerization by emodin: a novel AMPK activator with PPARγ-agonist activity

J Cell Biochem. 2012 Nov;113(11):3547-58. doi: 10.1002/jcb.24232.

Abstract

Adiponectin is an important insulin-sensitizing adipokine with multiple beneficial effects on obesity-associated medical complications. It is secreted from adipocytes into circulation as high, medium, and low molecular weight forms (HMW, MMW, and LMW). Each oligomeric form of adiponectin exerts non-overlapping biological functions, with the HMW oligomer possessing the most potent insulin-sensitizing activity. In this study, we reported that emodin, a natural product and active ingredient of various Chinese herbs, activates AMPK in both 3T3-L1 adipocytes and 293T cells. Activation of AMPK by emodin promotes the assembly of HMW adiponectin and increases the ratio of HMW adiponectin to total adiponectin in 3T1-L1 adipocytes. Emodin might activate AMPK by an indirect mechanism similar to berberine. We also found that emodin activates PPARγ and promotes differentiation and adiponectin expression during differentiation of 3T3-L1 preadipocytes. Therefore, emodin is a novel AMPK activator with PPARγ-agonist activity. Our results demonstrate that the effects of emodin on adiponectin expression and multimerization are the ultimate effects resulting from both AMPK activation and PPARγ activation. The dual-activity makes emodin or the derivatives potential drug candidates for the treatment of type 2 diabetes and other obesity-related metabolic diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Adipocytes / enzymology
  • Adiponectin / genetics
  • Adiponectin / metabolism*
  • Animals
  • Cell Line
  • Emodin / pharmacology*
  • Enzyme Activation / drug effects
  • Gene Expression Regulation / drug effects
  • Genes, Reporter
  • HEK293 Cells
  • Humans
  • Luciferases
  • Mice
  • Molecular Weight
  • PPAR gamma / agonists*
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Protein Multimerization / drug effects
  • Signal Transduction / drug effects

Substances

  • Adiponectin
  • PPAR gamma
  • Protein Isoforms
  • Protein Kinase Inhibitors
  • Luciferases
  • Protein Kinases
  • AMP-Activated Protein Kinase Kinases
  • Emodin