Beneficial effects of beta-sitosterol on glucose and lipid metabolism in L6 myotube cells are mediated by AMP-activated protein kinase

Biochem Biophys Res Commun. 2008 Dec 26;377(4):1253-8. doi: 10.1016/j.bbrc.2008.10.136. Epub 2008 Nov 4.

Abstract

AMP-activated protein kinase (AMPK) is an energy-sensing enzyme that has been implicated as a key factor for controlling intracellular lipids and glucose metabolism. Beta-sitosterol, a plant sterol known to prevent cardiovascular disease was identified from Schizonepeta tenuifolia to an AMPK activator. In L6 myotube cells, beta-sitosterol significantly increased phosphorylation of the AMPKalpha subunit and acetyl-CoA carboxylase (ACC) with stimulating glucose uptake. In contrast, beta-sitosterol treatment reduced intracellular levels of triglycerides and cholesterol in L6 cells. These effects were all reversed by pretreatment with AMPK inhibitor Compound C or LKB1 destabilizer radicicol. Similarly, beta-sitosterol-induced phosphorylation of AMPK and ACC was not increased in HeLa cells lacking LKB1. These results together suggest that beta-sitosterol-mediated enhancement of glucose uptake and reduction of triglycerides and cholesterol in L6 cells is predominantly accomplished by LKB1-mediated AMPK activation. Our findings further reveal a molecular mechanism underlying the beneficial effects of beta-sitosterol on glucose and lipid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • AMP-Activated Protein Kinases / metabolism*
  • Animals
  • Cell Line
  • Cholesterol / metabolism
  • Enzyme Activation
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • Humans
  • Hypolipidemic Agents / pharmacology*
  • Lipid Metabolism / drug effects*
  • Muscle Fibers, Skeletal / drug effects*
  • Muscle Fibers, Skeletal / metabolism
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Transport / drug effects
  • Rats
  • Signal Transduction / drug effects
  • Sitosterols / pharmacology*
  • Triglycerides / metabolism

Substances

  • Glucose Transporter Type 4
  • Hypolipidemic Agents
  • Sitosterols
  • Triglycerides
  • gamma-sitosterol
  • Cholesterol
  • Protein Serine-Threonine Kinases
  • Stk11 protein, rat
  • AMP-Activated Protein Kinase Kinases
  • AMP-Activated Protein Kinases
  • Glucose