Mechanism of nitrofurantoin toxicity and oxidative stress in mitochondria

Biochim Biophys Acta. 1988 Oct 26;936(1):139-47. doi: 10.1016/0005-2728(88)90261-7.

Abstract

5-Nitrofuran derivatives change the inner mitochondrial membrane permeability as indicated by the transmembrane potential, the rate of spontaneous K+ efflux and the basal respiratory rate: (a) at low concentrations nitrofurantoin prevents the increase of inner membrane permeability due to hydroperoxides or to diamide; (b) at higher concentrations or after longer times of incubation, nitrofurantoin enhances the membrane damage due to hydroperoxides or to diamide; the damage due Ca2+ plus Pi is enhanced by nitrofurantoin at all concentrations; (c) higher nitrofurantoin concentrations cause membrane damage independently of the presence of hydroperoxides or of diamide. The effect of nitrofurantoin is cancelled by the addition of free-radical scavengers. The above effects of nitrofurantoin are compatible with the observations of Mason and colleagues that nitrofurantoin is reduced by a NADPH nitroreductase to a nitro anion radical which can then undergo subsequent reactions, among which are (a) initiation of a free-radical reaction chain and (b) reduction of hydroperoxides and diamide.

MeSH terms

  • Animals
  • Calcium / pharmacology
  • Cell Membrane Permeability / drug effects
  • Diamide / pharmacology
  • Hydrogen Peroxide / pharmacology
  • Intracellular Membranes / metabolism
  • Kinetics
  • Membrane Potentials / drug effects
  • Mitochondria, Liver / drug effects*
  • Mitochondria, Liver / metabolism
  • Nitrofurantoin / pharmacology*
  • Oxygen Consumption / drug effects
  • Phosphates / pharmacology
  • Potassium / metabolism
  • Rats

Substances

  • Phosphates
  • Diamide
  • Nitrofurantoin
  • Hydrogen Peroxide
  • Potassium
  • Calcium