Chronic intake of proanthocyanidins and docosahexaenoic acid improves skeletal muscle oxidative capacity in diet-obese rats

J Nutr Biochem. 2014 Oct;25(10):1003-10. doi: 10.1016/j.jnutbio.2014.05.003. Epub 2014 Jun 5.

Abstract

Obesity has become a worldwide epidemic. The cafeteria diet (CD) induces obesity and oxidative-stress-associated insulin resistance. Polyunsaturated fatty acids and polyphenols are dietary compounds that are intensively studied as products that can reduce the health complications related to obesity. We evaluate the effects of 21 days of supplementation with grape seed proanthocyanidins extract (GSPE), docosahexaenoic-rich oil (DHA-OR) or both compounds (GSPE+DHA-OR) on skeletal muscle metabolism in diet-obese rats. The supplementation with different treatments did not reduce body weight, although all groups used more fat as fuel, particularly when both products were coadministered; muscle β-oxidation was activated, the mitochondrial functionality and oxidative capacity were higher, and fatty acid uptake gene expressions were up-regulated. In addition to these outcomes shared by all treatments, GSPE reduced insulin resistance and improved muscle status. Both treatments increased 5'-AMP-activated protein kinase (AMPK) phosphorylation, which was consistent with higher plasma adiponectin levels. Moreover, AMPK activation by DHA-OR was also correlated with an up-regulation of peroxisome proliferator-activated receptor alpha (Pparα). GSPE+DHA-OR, in addition to activating AMPK and enhancing fatty acid oxidation, increased the muscle gene expression of uncoupling protein 2 (Ucp2). In conclusion, GSPE+DHA-OR induced modifications that improved muscle status and could counterbalance the deleterious effects of obesity, and such modifications are mediated, at least in part, through the AMPK signaling pathway.

Keywords: Docosahexaenoic acid; Mitochondria; Obesity; Proanthocyanidins; Skeletal muscle; β-Oxidation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Adiponectin / blood
  • Animals
  • Body Weight
  • Calorimetry, Indirect
  • Creatine Kinase / blood
  • Docosahexaenoic Acids / pharmacology*
  • Grape Seed Extract / pharmacology*
  • Insulin Resistance
  • Ion Channels / genetics
  • Ion Channels / metabolism
  • Lipid Metabolism / drug effects*
  • Male
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism*
  • Obesity / drug therapy
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • Phosphorylation
  • Proanthocyanidins / pharmacology*
  • Rats
  • Rats, Wistar
  • Uncoupling Protein 2
  • Up-Regulation

Substances

  • Adiponectin
  • Grape Seed Extract
  • Grape Seed Proanthocyanidins
  • Ion Channels
  • Mitochondrial Proteins
  • PPAR alpha
  • Proanthocyanidins
  • Ucp2 protein, rat
  • Uncoupling Protein 2
  • Docosahexaenoic Acids
  • AMP-Activated Protein Kinases
  • Creatine Kinase