Anthocyanins from Purple Corn Ameliorated Tumor Necrosis Factor-α-Induced Inflammation and Insulin Resistance in 3T3-L1 Adipocytes via Activation of Insulin Signaling and Enhanced GLUT4 Translocation

Mol Nutr Food Res. 2017 Dec;61(12). doi: 10.1002/mnfr.201700362. Epub 2017 Sep 19.

Abstract

Scope: The aim was to compare the effect of an anthocyanin-rich extract from purple corn pericarp (PCW) and pure anthocyanins on adipogenesis, inflammation, and insulin resistance in 3T3-L1 adipocytes on basal and inflammatory conditions.

Methods and results: Preadipocytes (3T3-L1) were treated during differentiation with or without PCW. Differentiated adipocytes were treated either individually or in combination with tumor necrosis factor α (TNF-α) and PCW, or pure C3G, Pr3G, P3G. PCW reduced preadipocyte differentiation (IC50 = 0.4 mg/mL). PCW and pure anthocyanins including C3G reduced fatty acid synthase enzymatic activity. PCW reduced TNF-α-dependent inflammatory status increasing adiponectin (39%), and decreasing leptin (-79%). PCW and C3G increased glucose uptake and reduced reactive oxygen species generation in insulin resistant adipocytes. An increase in phosphorylation was observed in AKT, IKK, and MEK, and a decrease in IRS and mTOR activating the insulin receptor-associated pathway. PCW (7.5-fold) and C3G (6.3-fold) enhanced GLUT4 membrane translocation compared to insulin resistant adipocytes.

Conclusion: Anthocyanins from colored corn prevented adipocyte differentiation, lipid accumulation, and reduced PPAR-γ transcriptional activity on adipocytes in basal conditions. Ameliorated TNF-α-induced inflammation and insulin resistance in adipocytes via activation of insulin signaling and enhanced GLUT4 translocation suggesting a reduced hyperglycemia associated with the metabolic syndrome.

Keywords: anthocyanins; inflammation; obesity; polyphenols; purple corn.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Animals
  • Anthocyanins / pharmacology*
  • Cell Differentiation / drug effects
  • Enzymes / metabolism
  • Glucose Transporter Type 4 / metabolism*
  • Inflammation / drug therapy*
  • Inflammation / metabolism
  • Insulin / metabolism
  • Insulin Resistance
  • Lipid Metabolism / drug effects
  • Mice
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Protein Transport
  • Tumor Necrosis Factor-alpha / toxicity*
  • Zea mays / chemistry*

Substances

  • Anthocyanins
  • Enzymes
  • Glucose Transporter Type 4
  • Insulin
  • Plant Extracts
  • Slc2a4 protein, mouse
  • Tumor Necrosis Factor-alpha