Antioxidant enzyme gene transcription in copper-deficient rat liver

Free Radic Biol Med. 1996;21(2):233-40. doi: 10.1016/0891-5849(96)00029-9.

Abstract

Antioxidant enzymes, Cu/Zn- and Mn-superoxide dismutase, catalase, and glutathione peroxidase, constitute an important defense mechanism against cytotoxicity of reactive oxygen species. Copper is essential for the activity of Cu/Zn-superoxide dismutase. Oxidative stress, therefore, is expected in organs of rats fed copper-deficient diet due to reduced Cu/Zn-superoxide dismutase activity. Our previous studies have shown that the expression of antioxidant enzymes was altered in copper-deficient rat liver. The present report was undertaken to study further the transcription of these enzymes in liver nuclei of rats made copper-deficient for 4 weeks. While copper deficiency decreased the copper in liver by about 80%, it did not alter the copper content in liver nuclei. In spite of a 100% elevation in nuclear iron concentration, liver nuclei from copper-deficient rats showed normal appearance. The transcriptional rates for Cu/Zn-superoxide dismutase, glutathione peroxidase, and glyceraldehyde-3-phosphate dehydrogenase were not altered by dietary copper deprivation. In contrast, transcriptional rates for Mn-superoxide dismutase and beta-actin were increased but that for catalase was reduced in the nuclei isolated from the copper-deficient rat liver. These results suggest that oxidative stress, resulting from copper deficiency, differentially modulates the gene transcription for the antioxidant enzymes in rat liver.

Publication types

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

MeSH terms

  • Animals
  • Body Weight
  • Catalase / genetics*
  • Copper / deficiency*
  • Copper / metabolism
  • Glutathione Peroxidase / genetics*
  • Iron / metabolism
  • Liver / enzymology*
  • Liver / pathology
  • Male
  • Microscopy, Electron
  • Myocardium / pathology
  • Organ Size
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / genetics*
  • Transcription, Genetic

Substances

  • Copper
  • Iron
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase