An ethanol extract of Artemisia iwayomogi activates PPARδ leading to activation of fatty acid oxidation in skeletal muscle

PLoS One. 2012;7(3):e33815. doi: 10.1371/journal.pone.0033815. Epub 2012 Mar 27.

Abstract

Although Artemisia iwayomogi (AI) has been shown to improve the lipid metabolism, its mode of action is poorly understood. In this study, a 95% ethanol extract of AI (95EEAI) was identified as a potent ligand of peroxisome proliferator-activated receptorδ (PPARδ) using ligand binding analysis and cell-based reporter assay. In cultured primary human skeletal muscle cells, treatment of 95EEAI increased expression of two important PPARδ-regulated genes, carnitine palmitoyl-transferase-1 (CPT1) and pyruvate dehydrogenase kinase isozyme 4 (PDK4), and several genes acting in lipid efflux and energy expenditure. Furthermore, 95EEAI stimulated fatty acid oxidation in a PPARδ-dependent manner. High-fat diet-induced obese mice model further indicated that administration of 95EEAI attenuated diet-induced obesity through the activation of fatty acid oxidation in skeletal muscle. These results suggest that a 95% ethanol extract of AI may have a role as a new functional food material for the prevention and/or treatment of hyperlipidermia and obesity.

MeSH terms

  • Animals
  • Artemisia / chemistry*
  • Diet, High-Fat / adverse effects
  • Ethanol / chemistry
  • Fatty Acids / metabolism*
  • Gene Expression Regulation / drug effects
  • Glucose / metabolism
  • Humans
  • Kinetics
  • Ligands
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism*
  • Obesity / drug therapy
  • Obesity / metabolism
  • Oxidation-Reduction / drug effects
  • PPAR delta / metabolism*
  • Plant Extracts / administration & dosage
  • Plant Extracts / pharmacology*
  • Protein Binding
  • Transcriptional Activation / drug effects

Substances

  • Fatty Acids
  • Ligands
  • PPAR delta
  • Plant Extracts
  • Ethanol
  • Glucose