Hypoxia in vivo decreases peroxisome proliferator-activated receptor alpha-regulated gene expression in rat heart

Biochem Biophys Res Commun. 2001 Sep 14;287(1):5-10. doi: 10.1006/bbrc.2001.5541.

Abstract

We tested the hypothesis that hypoxia decreases PPARalpha-regulated gene expression in heart muscle in vivo. In two rat models of systemic hypoxia (cobalt chloride treatment and iso-volemic hemodilution), transcript levels of PPARalpha and PPARalpha-regulated genes (pyruvate dehydrogenase kinase 4 (PDK4), muscle carnitine palmitoyltransferase-I (mCPT-I), and malonyl-CoA decarboxylase (MCD)) were measured using real-time quantitative RT-PCR. Data were normalized to the housekeeping gene beta-actin. Atrial natriuretic factor (ANF) and pyruvate dehydrogenase kinase 2 (PDK2), which are not regulated by PPARalpha, served as controls. CoCl(2) treatment decreased PPARalpha, PDK4, mCPT-I, and MCD mRNA levels. Iso-volemic anemia also caused a significant decrease in PPARalpha, PDK4, and MCD mRNA levels. Transcript levels of mCPT-I showed a slight, but not significant decrease (P = 0.08). Gene expression of beta-actin, ANF, and PDK2 did not change with either CoCl(2) treatment nor with anemia. Myocardial PPARalpha-regulated gene expression is decreased in two models of hypoxia in vivo. These results suggest a transcriptional mechanism for decreased fatty oxidation and increased reliance of the heart for glucose during hypoxia.

Publication types

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

MeSH terms

  • Animals
  • Carboxy-Lyases / metabolism
  • Carnitine O-Palmitoyltransferase / metabolism
  • Cobalt / pharmacology*
  • Down-Regulation
  • Energy Metabolism
  • Gene Expression* / drug effects
  • Heart / drug effects
  • Heart / physiology*
  • Hemodilution
  • Hypoxia
  • Isoenzymes / metabolism
  • Male
  • Myocardium / metabolism*
  • Oxygen / metabolism*
  • Protein Kinases / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*

Substances

  • Isoenzymes
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Cobalt
  • Carnitine O-Palmitoyltransferase
  • Protein Kinases
  • pyruvate dehydrogenase kinase 4
  • Carboxy-Lyases
  • malonyl-CoA decarboxylase
  • cobaltous chloride
  • Oxygen