Neuroprotective activity of p-terphenyl leucomentins from the mushroom Paxillus panuoides

Biosci Biotechnol Biochem. 2003 Aug;67(8):1813-6. doi: 10.1271/bbb.67.1813.

Abstract

The neuroprotective mechanism of p-terphenyl leucomentins from the mushroom Paxillus panuoides was studied. Leucomentins showed potent inhibition of lipid peroxidation and H2O2 neurotoxicity, but free from any role as reactive oxygen species (ROS) scavengers. Iron-mediated oxidative damage has been implicated in these processes, as a provider of ROS via iron. Leucomentins can chelate iron when DNA is present with iron and H2O2, and so inhibiting DNA single strand breakage. These results suggest that the neuroprotective action of leucomentins is dependent on their ability to chelate iron.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agaricales / chemistry*
  • Alkenes / chemistry
  • Alkenes / pharmacology*
  • Animals
  • DNA Damage / drug effects
  • Epoxy Compounds / chemistry
  • Epoxy Compounds / pharmacology*
  • Ferrous Compounds / metabolism
  • Ferrous Compounds / toxicity
  • Free Radicals / metabolism
  • Glutamic Acid / metabolism
  • Glutamic Acid / toxicity
  • Hydrogen Peroxide / metabolism
  • Hydrogen Peroxide / toxicity
  • Iron Chelating Agents / chemistry
  • Iron Chelating Agents / pharmacology
  • Lipid Peroxidation / drug effects
  • Mice
  • Mice, Inbred ICR
  • N-Methylaspartate / metabolism
  • N-Methylaspartate / toxicity
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism
  • Neuroprotective Agents / chemistry
  • Neuroprotective Agents / pharmacology*
  • Rats
  • Terphenyl Compounds / chemistry
  • Terphenyl Compounds / pharmacology*

Substances

  • Alkenes
  • Epoxy Compounds
  • Ferrous Compounds
  • Free Radicals
  • Iron Chelating Agents
  • Neuroprotective Agents
  • Terphenyl Compounds
  • leucomentin-5
  • leucomentin-6
  • Glutamic Acid
  • N-Methylaspartate
  • Hydrogen Peroxide