Cyanidin 3-glucoside ameliorates hyperglycemia and insulin sensitivity due to downregulation of retinol binding protein 4 expression in diabetic mice

Biochem Pharmacol. 2007 Dec 3;74(11):1619-27. doi: 10.1016/j.bcp.2007.08.008. Epub 2007 Aug 10.

Abstract

Adipocyte dysfunction is strongly associated with the development of obesity and insulin resistance. It is accepted that the regulation of adipocytokine expression is one of the most important targets for the prevention of obesity and improvement of insulin sensitivity. In this study, we have demonstrated that anthocyanin (cyanidin 3-glucoside; C3G) which is a pigment widespread in the plant kingdom, ameliorates hyperglycemia and insulin sensitivity due to the reduction of retinol binding protein 4 (RBP4) expression in type 2 diabetic mice. KK-A(y) mice were fed control or control +0.2% of a C3G diet for 5 weeks. Dietary C3G significantly reduced blood glucose concentration and enhanced insulin sensitivity. The adiponectin and its receptors expression were not responsible for this amelioration. C3G significantly upregulated the glucose transporter 4 (Glut4) and downregulated RBP4 in the white adipose tissue, which is accompanied by downregulation of the inflammatory adipocytokines (monocyte chemoattractant protein-1 and tumor necrosis factor-alpha) in the white adipose tissue of the C3G group. These findings indicate that C3G has significant potency in an anti-diabetic effect through the regulation of Glut4-RBP4 system and the related inflammatory adipocytokines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipokines / genetics
  • Adipokines / metabolism
  • Adiponectin / genetics
  • Adiponectin / metabolism
  • Adipose Tissue, White / drug effects
  • Adipose Tissue, White / metabolism
  • Animals
  • Anthocyanins / chemistry
  • Anthocyanins / pharmacology*
  • Anthocyanins / therapeutic use
  • Blood Glucose / metabolism
  • Blotting, Western
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / metabolism
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Glucose Tolerance Test
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism
  • Glucose-6-Phosphatase / metabolism
  • Glucosides / chemistry
  • Glucosides / pharmacology*
  • Glucosides / therapeutic use
  • Hyperglycemia / blood
  • Hyperglycemia / drug therapy*
  • Inflammation Mediators / antagonists & inhibitors
  • Inflammation Mediators / metabolism
  • Insulin Resistance / physiology*
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred Strains
  • Molecular Structure
  • Receptors, Adiponectin / genetics
  • Receptors, Adiponectin / metabolism
  • Retinol-Binding Proteins, Plasma / genetics
  • Retinol-Binding Proteins, Plasma / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Adipokines
  • Adiponectin
  • Anthocyanins
  • Blood Glucose
  • Glucose Transporter Type 4
  • Glucosides
  • Inflammation Mediators
  • Rbp4 protein, mouse
  • Receptors, Adiponectin
  • Retinol-Binding Proteins, Plasma
  • cyanidin-3-O-beta-glucopyranoside
  • Glucose-6-Phosphatase