Berberine-induced activation of AMPK increases hepatic FGF21 expression via NUR77

Biochem Biophys Res Commun. 2018 Jan 8;495(2):1936-1941. doi: 10.1016/j.bbrc.2017.12.070. Epub 2017 Dec 13.

Abstract

Fibroblast growth factor 21 (FGF21), a hormone-like protein mainly derived from liver, exhibits multiple beneficial effect on energy metabolism. Similar to FGF21, berberine exerts anti-hyperglycemic and anti-dyslipidemic properties. Previous studies revealed that the beneficial metabolic effect of berberine was attributed to the activation of AMP-activated protein kinase (AMPK). Here we investigated the effect of berberine on FGF21 expression in primary mouse hepatocytes. As expected, berberine induced hepatic FGF21 expression in a dose-dependent and time-dependent manner, along with the increased expression of NUR77, a proved transcription factor of FGF21. Berberine stimulated the phosphorylations of AMPK and acetyl-CoA carboxylase in primary mouse hepatocytes. Adenovirus-mediated overexpression of constitutively active AMPK triggered hepatic FGF21 and NUR77 expressions. The inhibition of AMPK by compound C abolished berberine-stimulated FGF21 and NUR77 expressions. These results suggest that berberine-induced activation of AMPK may contribute to hepatic FGF21 expression via NUR77.

Keywords: AMP-activated protein kinase; Berberine; Fibroblast growth factor 21; Hepatocytes; NUR77.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Animals
  • Berberine / administration & dosage*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Enzyme Activation / drug effects
  • Enzyme Activation / physiology
  • Fibroblast Growth Factors / metabolism*
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • Hypoglycemic Agents / administration & dosage
  • Hypolipidemic Agents / administration & dosage
  • Male
  • Metabolic Networks and Pathways / drug effects
  • Metabolic Networks and Pathways / physiology
  • Mice
  • Mice, Inbred C57BL
  • Nuclear Receptor Subfamily 4, Group A, Member 1 / metabolism*
  • Protein Kinases / metabolism*
  • Up-Regulation / drug effects
  • Up-Regulation / physiology

Substances

  • Hypoglycemic Agents
  • Hypolipidemic Agents
  • Nr4a1 protein, mouse
  • Nuclear Receptor Subfamily 4, Group A, Member 1
  • fibroblast growth factor 21
  • Berberine
  • Fibroblast Growth Factors
  • Protein Kinases
  • AMP-Activated Protein Kinase Kinases