Effects of phenyl derivatives of dihydropyrazines with ability to generate radical species on Escherichia coli

Biol Pharm Bull. 2007 Sep;30(9):1663-7. doi: 10.1248/bpb.30.1663.

Abstract

Phenyl-substituted dihydropyrazines (Ph-DHPs) are derivatives of 2,3-dihydro-5,6-dimethylpyrazine (Me-DHP). Upon the addition of Cu(2+), Me-DHP inhibits the growth of Escherichia coli by generating hydroxyl and carbon-centered radicals that cause DNA strand breakage. Here, we investigated the toxic effect of Ph-DHPs in several DNA repair-deficient or detoxifying enzyme-deficient mutant strains. Ph-DHPs caused cytotoxic and genotoxic damage, but, in a sodA sodB strain, the effects in the presence or absence of Cu(2+) were different than those of Me-DHP. Our results suggest that the action of the generated superoxide anion in the interior side of the cell is remarkable.

MeSH terms

  • Aminolevulinic Acid / metabolism
  • Copper / pharmacology
  • DNA / drug effects
  • DNA / genetics
  • DNA Repair / drug effects
  • Electron Spin Resonance Spectroscopy
  • Escherichia coli K12 / drug effects
  • Escherichia coli K12 / genetics
  • Escherichia coli K12 / metabolism*
  • Liver Neoplasms / chemically induced
  • Liver Neoplasms / pathology
  • Mutation
  • Phenyl Ethers / chemistry
  • Phenyl Ethers / metabolism
  • Pyrazines / chemistry
  • Pyrazines / pharmacology*
  • Tetrazolium Salts / metabolism

Substances

  • 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium
  • Phenyl Ethers
  • Pyrazines
  • Tetrazolium Salts
  • Copper
  • Aminolevulinic Acid
  • DNA