Resistance of hepatic lysosomes, mitochondria and microsomes of protoporphyrin-administered rats to peroxidative damage

Biol Pharm Bull. 1995 Jun;18(6):913-6. doi: 10.1248/bpb.18.913.

Abstract

Antioxidative inhibition by protoporphyrin (PP) of peroxidative damage in lysosomes, mitochondria and microsomes of rat liver was investigated at 24 h after an intravenous administration of PP. Using a lysosome-containing (3500 x g) fraction, the release of lysosomal marker enzymes, acid phosphatase and aryl sulfatase, from lysosome which had been stimulated by L-ascorbic acid (AsA), was decreased dose-dependently, as was the inhibition of lipid peroxidation by PP in the fraction. Swelling of mitochondria induced by Fe2+ and AsA was also inhibited in the PP-injected rat. In microsomes, lipid peroxidation stimulated by AsA caused a decrease in activity of a microsomal marker enzyme, glucose 6-phosphatase, and in P450 content. The extent of the decrease by AsA, both in activity and content, was diminished in PP-administered rat liver microsomes. These results indicate that PP protects those subcellular fractions from deterioration by lipid peroxidation.

MeSH terms

  • Animals
  • Biomarkers
  • Cytochrome P-450 Enzyme System / metabolism
  • Glucosephosphate Dehydrogenase / antagonists & inhibitors
  • Glucosephosphate Dehydrogenase / metabolism
  • In Vitro Techniques
  • Iron / pharmacology
  • Lipid Peroxidation / drug effects*
  • Liver / drug effects
  • Liver / enzymology
  • Liver / metabolism*
  • Lysosomes / drug effects*
  • Lysosomes / enzymology
  • Male
  • Membranes / drug effects
  • Microsomes, Liver / drug effects*
  • Microsomes, Liver / enzymology
  • Mitochondria, Liver / drug effects*
  • Mitochondria, Liver / enzymology
  • Mitochondrial Swelling / drug effects
  • Protoporphyrins / pharmacology*
  • Rats
  • Rats, Wistar

Substances

  • Biomarkers
  • Protoporphyrins
  • Cytochrome P-450 Enzyme System
  • Iron
  • Glucosephosphate Dehydrogenase