Cyanidin-3-O-glucoside restores insulin signaling and reduces inflammation in hypertrophic adipocytes

Arch Biochem Biophys. 2020 Sep 30:691:108488. doi: 10.1016/j.abb.2020.108488. Epub 2020 Jul 18.

Abstract

Obesity is a metabolic disorder characterized by excess adipose tissue, macrophages infiltration, and inflammation which in turn lead to insulin-resistance. Epidemiological evidences reported that anthocyanins possess not only high antioxidant and antiinflammatory activities, but also improve metabolic complications associated with obesity. The aim of this work was to evaluate the in vitro beneficial effects of cyanidin-3-O-glucoside (C3G) in counteracting inflammation and insulin-resistance in 3T3-L1 hypertrophic adipocytes exposed to palmitic acid (PA). In the present study murine 3T3-L1 adipocytes were pretreated with C3G for 24 h and then exposed to palmitic acid (PA) for 24 h. Real-time PCR, western blotting analysis and Oil Red O staining were applied for investigating the mechanism involved in adipocytes dysfunction. C3G pretreatment reduced lipid accumulation, PPARγ pathway and NF-κB pathway induced by PA in murine adipocytes. In addition, our data demonstrated that PA reduced insulin signaling via IRS-1 Ser307phosphorylation while C3G dose-dependently improved insulin sensitivity restoring IRS-1/PI3K/Akt pathway. Furthermore, C3G improved adiponectin mRNA levels altered by PA in 3T3-L1 murine and SGBS human adipocytes. Herein reported data demonstrate that C3G ameliorated adipose tissue dysfunction, thus suggesting new potential roles for this compound of nutritional interest in the prevention of pathological conditions linked to obesity.

Keywords: Adipocytes; Anthocyanin; Inflammation; Insulin-resistance; Palmitic acid.

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects*
  • Adipogenesis / drug effects
  • Adiponectin / metabolism
  • Animals
  • Anthocyanins / pharmacology*
  • Fatty Acid-Binding Proteins / metabolism
  • Glucose Transporter Type 1 / metabolism
  • Glucosides / pharmacology*
  • Humans
  • Inflammation / prevention & control*
  • Insulin Resistance / physiology
  • Mice
  • NF-kappa B / metabolism
  • PPAR gamma / metabolism
  • Palmitic Acid / pharmacology
  • Signal Transduction / drug effects*

Substances

  • Adiponectin
  • Anthocyanins
  • Fabp4 protein, mouse
  • Fatty Acid-Binding Proteins
  • Glucose Transporter Type 1
  • Glucosides
  • NF-kappa B
  • PPAR gamma
  • Slc2a1 protein, mouse
  • cyanidin-3-O-beta-glucopyranoside
  • Palmitic Acid