A polyphenol rescues lipid induced insulin resistance in skeletal muscle cells and adipocytes

Biochem Biophys Res Commun. 2014 Sep 26;452(3):382-8. doi: 10.1016/j.bbrc.2014.08.079. Epub 2014 Aug 23.

Abstract

Skeletal muscle and adipose tissues are known to be two important insulin target sites. Therefore, lipid induced insulin resistance in these tissues greatly contributes in the development of type 2 diabetes (T2D). Ferulic acid (FRL) purified from the leaves of Hibiscus mutabilis, showed impressive effects in preventing saturated fatty acid (SFA) induced defects in skeletal muscle cells. Impairment of insulin signaling molecules by SFA was significantly waived by FRL. SFA markedly reduced insulin receptor β (IRβ) in skeletal muscle cells, this was affected due to the defects in high mobility group A1 (HMGA1) protein obtruded by phospho-PKCε and that adversely affects IRβ mRNA expression. FRL blocked PKCε activation and thereby permitted HMGA1 to activate IRβ promoter which improved IR expression deficiency. In high fat diet (HFD) fed diabetic rats, FRL reduced blood glucose level and enhanced lipid uptake activity of adipocytes isolated from adipose tissue. Importantly, FRL suppressed fetuin-A (FetA) gene expression, that reduced circulatory FetA level and since FetA is involved in adipose tissue inflammation, a significant attenuation of proinflammatory cytokines occurred. Collectively, FRL exhibited certain unique features for preventing lipid induced insulin resistance and therefore promises a better therapeutic choice for T2D.

Keywords: Ferulic acid; Fetuin-A; Insulin receptor; Insulin resistance; PKCε; SFA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adipose Tissue / drug effects*
  • Adipose Tissue / metabolism
  • Animals
  • Coumaric Acids / isolation & purification
  • Coumaric Acids / pharmacology*
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / etiology
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism
  • Diet, High-Fat
  • Fatty Acids / adverse effects
  • Gene Expression Regulation
  • HMGA1a Protein / agonists
  • HMGA1a Protein / genetics
  • HMGA1a Protein / metabolism
  • Hibiscus / chemistry*
  • Hypoglycemic Agents / isolation & purification
  • Hypoglycemic Agents / pharmacology*
  • Insulin Resistance
  • Male
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / metabolism
  • Plant Leaves / chemistry
  • Promoter Regions, Genetic
  • Protein Kinase C-epsilon / antagonists & inhibitors
  • Protein Kinase C-epsilon / genetics
  • Protein Kinase C-epsilon / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Insulin / agonists
  • Receptor, Insulin / antagonists & inhibitors
  • Receptor, Insulin / genetics
  • Receptor, Insulin / metabolism
  • Signal Transduction
  • alpha-2-HS-Glycoprotein / antagonists & inhibitors
  • alpha-2-HS-Glycoprotein / genetics
  • alpha-2-HS-Glycoprotein / metabolism

Substances

  • Coumaric Acids
  • Fatty Acids
  • Hypoglycemic Agents
  • alpha-2-HS-Glycoprotein
  • HMGA1a Protein
  • ferulic acid
  • Receptor, Insulin
  • Protein Kinase C-epsilon