Prevention mechanisms of glucose intolerance and obesity by cacao liquor procyanidin extract in high-fat diet-fed C57BL/6 mice

Arch Biochem Biophys. 2012 Nov 15;527(2):95-104. doi: 10.1016/j.abb.2012.03.018. Epub 2012 Mar 23.

Abstract

In this study, we investigated whether cacao liquor procyanidin (CLPr) extract, which consists of 4.3% catechin, 6.1% epicatechin, 39.4% procyanidins and others, ameliorated hyperglycemia and obesity in C57BL/6 mice fed a control or high-fat diet for 13 weeks. CLPr suppressed high-fat diet-induced hyperglycemia, glucose intolerance and fat accumulation in white adipose tissue. CLPr also promoted translocation of glucose transporter 4 (GLUT4) and phosphorylation of AMP-activated protein kinase α (AMPKα) in the plasma membrane of skeletal muscle and brown adipose tissue. Phosphorylation of AMPKα was also enhanced in the liver and white adipose tissue. CLPr up-regulated the gene and protein expression levels of uncoupling protein (UCP)-1 in brown adipose tissue and UCP-3 in skeletal muscle. These results indicate that CLPr is a beneficial food material for the prevention of hyperglycemia and obesity. Activation of AMPKα, translocation of GLUT4 and up-regulation of UCP expression in skeletal muscle and adipose tissue are involved in the molecular mechanisms by which CLPr prevents hyperglycemia and obesity.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Adipokines / blood
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism
  • Animals
  • Biflavonoids / pharmacology*
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Cacao / chemistry*
  • Catechin / pharmacology*
  • Diet, High-Fat / adverse effects*
  • Energy Metabolism / drug effects
  • Enzyme Activation / drug effects
  • Gene Expression Regulation / drug effects
  • Glucose Intolerance / etiology
  • Glucose Intolerance / metabolism
  • Glucose Intolerance / pathology
  • Glucose Intolerance / prevention & control*
  • Glucose Transporter Type 4 / metabolism
  • Insulin Resistance
  • Ion Channels / genetics
  • Ion Channels / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Obesity / chemically induced
  • Obesity / metabolism
  • Obesity / pathology
  • Obesity / prevention & control*
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Phosphorylation / drug effects
  • Proanthocyanidins / pharmacology*
  • Protein Transport / drug effects
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors
  • Uncoupling Protein 1

Substances

  • Adipokines
  • Biflavonoids
  • Blood Glucose
  • Glucose Transporter Type 4
  • Ion Channels
  • Mitochondrial Proteins
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, mouse
  • Proanthocyanidins
  • Trans-Activators
  • Transcription Factors
  • Ucp1 protein, mouse
  • Uncoupling Protein 1
  • procyanidin
  • Catechin
  • AMP-Activated Protein Kinases