A gender-related defect in lipid metabolism and glucose homeostasis in peroxisome proliferator- activated receptor alpha- deficient mice

J Clin Invest. 1998 Sep 15;102(6):1083-91. doi: 10.1172/JCI3949.

Abstract

The peroxisome proliferator-activated receptor alpha (PPARalpha) is a nuclear receptor implicated in the control of cellular lipid utilization. To test the hypothesis that PPARalpha is activated as a component of the cellular lipid homeostatic response, the expression of PPARalpha target genes was characterized in response to a perturbation in cellular lipid oxidative flux caused by pharmacologic inhibition of mitochondrial fatty acid import. Inhibition of fatty acid oxidative flux caused a feedback induction of PPARalpha target genes encoding fatty acid oxidation enzymes in liver and heart. In mice lacking PPARalpha (PPARalpha-/-), inhibition of cellular fatty acid flux caused massive hepatic and cardiac lipid accumulation, hypoglycemia, and death in 100% of male, but only 25% of female PPARalpha-/- mice. The metabolic phenotype of male PPARalpha-/- mice was rescued by a 2-wk pretreatment with beta-estradiol. These results demonstrate a pivotal role for PPARalpha in lipid and glucose homeostasis in vivo and implicate estrogen signaling pathways in the regulation of cardiac and hepatic lipid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carbohydrate Metabolism, Inborn Errors / physiopathology*
  • Carnitine O-Palmitoyltransferase / antagonists & inhibitors
  • Epoxy Compounds / pharmacology
  • Estradiol / pharmacology
  • Fatty Acids / metabolism
  • Feedback*
  • Female
  • Glucose / metabolism*
  • Glycogen / metabolism
  • Hypoglycemia
  • Lipid Metabolism, Inborn Errors / physiopathology*
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism
  • Myocardium / metabolism
  • Oxidation-Reduction
  • Receptors, Cytoplasmic and Nuclear / deficiency*
  • Sex Factors*
  • Transcription Factors / deficiency*

Substances

  • Epoxy Compounds
  • Fatty Acids
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Estradiol
  • Glycogen
  • Carnitine O-Palmitoyltransferase
  • Glucose
  • etomoxir