Aspalathin improves glucose and lipid metabolism in 3T3-L1 adipocytes exposed to palmitate

Mol Nutr Food Res. 2015 Nov;59(11):2199-208. doi: 10.1002/mnfr.201500258. Epub 2015 Sep 15.

Abstract

Scope: Saturated-free fatty acids, such as palmitate, are associated with insulin resistance. This study aimed to establish if an aspalathin-enriched green rooibos extract (GRE) and, its major flavanoid, aspalathin (ASP) could contribute significantly to the amelioration of experimentally induced insulin resistance in 3T3-L1 adipocytes.

Methods and results: 3T3-L1 adipocytes were cultured in DMEM containing 0.75 mM palmitate for 16 h to induce insulin resistance before treatment for 3 h with GRE (10 μg/mL) or ASP (10 μM). GRE and ASP reversed the palmitate-induced insulin resistance. At a protein level GRE and ASP suppressed nuclear factor kappa beta (NF-κB), insulin receptor substrate one (serine 307) (IRS1 (Ser (307) )) and AMP-activated protein kinase phosphorylation and increased serine/threonine kinase AKT (AKT) activation, while only GRE increased glucose transporter four (Glut4) protein expression. Peroxisome proliferator-activated receptor alpha and gamma (PPARα and γ), and carnitine palmitoyltransferase one (CPT1) expression were increased by ASP alone.

Conclusion: Together these effects offer a plausible explanation for the ameliorative effect of GRE and ASP on insulin-resistance, an underlying cause for obesity and type 2 diabetes.

Keywords: Aspalathin; Aspalathus linearis; Dihydrochalcone C-glucoside; Insulin resistance; Palmitate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • AMP-Activated Protein Kinases / metabolism
  • Adenosine Triphosphate / metabolism
  • Animals
  • Aspalathus*
  • Chalcones / pharmacology*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / genetics
  • Insulin / pharmacology
  • Insulin Resistance
  • Lipid Metabolism / drug effects*
  • Mice
  • NF-kappa B / metabolism
  • Palmitates / pharmacology*
  • Plant Extracts / pharmacology*

Substances

  • Chalcones
  • Glucose Transporter Type 4
  • Insulin
  • NF-kappa B
  • Palmitates
  • Plant Extracts
  • Slc2a4 protein, mouse
  • aspalathin
  • Adenosine Triphosphate
  • AMP-Activated Protein Kinases
  • Glucose