Chronic in vivo hypoxia in various organs: hypoxia-inducible factor-1alpha and apoptosis

Biochem Biophys Res Commun. 2006 Apr 14;342(3):875-80. doi: 10.1016/j.bbrc.2006.02.042.

Abstract

We studied the in vivo persistence of hypoxia-inducible factor-1alpha (HIF-1alpha), main transducer of hypoxia, the differential response in organs exposed to the same degree of hypoxemia and the relationship with apoptosis. We measured HIF-1alpha (immunohistochemistry peroxidase and Western blot) and apoptosis (TUNEL) in heart, liver, kidney, gastrocnemius, and brain of rats exposed to chronic normobaric hypoxia (10% O2) or normoxia (21% O2) for 2 weeks. Despite same arterial O2 pressure and increased hemoglobin concentration (219 +/- 5 vs. 124 +/- 4 g/L), the organs responded differently. While marked in brain, muscle, and kidney cortex, HIF-1alpha was undetectable in heart and liver. In kidney medulla, HIF-1alpha was high in both normoxia and hypoxia. By contrast, apoptosis was marked in heart, slight in kidney medulla, and undetectable in other organs. We conclude that the HIF-1alpha response to chronic hypoxia can be a sustained phenomenon, but not in all organs, and that apoptosis responds differently from HIF-1alpha.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Brain / metabolism*
  • Cell Hypoxia / physiology*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Kidney Cortex / metabolism*
  • Muscles / metabolism*
  • Organ Specificity
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Hypoxia-Inducible Factor 1, alpha Subunit