Action of metal chelators on lipoxygenases, cyclooxygenase and on inflammation-induced vasodepression

Biomed Biochim Acta. 1988;47(10-11):S256-9.

Abstract

Metal complexing agents could exert antiinflammatory activity by inhibition of oxygen radical production, by inhibition of eicosanoid synthesis and by inhibition of metalloenzymes. We found a moderate antiedema activity of the iron (II)/iron (III)-chelator combination, o-phenanthroline/desferrioxamine, which could refer to an involvement of iron ions in the inflammatory reaction. The newly synthetized complexing agent ethylene-diimino-dibutyric acid caused weak antiedema and antivasodepressor effects which remain to be explained. Altogether, the in vivo effects of the metal chelators were rather weak. In vitro, only desferrioxamine produced a remarkable inhibition of two lipoxygenases.

MeSH terms

  • Animals
  • Arthritis / physiopathology*
  • Arthritis, Experimental / physiopathology*
  • Blood Pressure / drug effects
  • Chelating Agents / pharmacology
  • Chelating Agents / therapeutic use*
  • Edema / prevention & control*
  • Inflammation / physiopathology
  • Inflammation / prevention & control
  • Iron Chelating Agents / pharmacology
  • Iron Chelating Agents / therapeutic use*
  • Lipoxygenase / metabolism*
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Rats
  • Vascular Resistance / drug effects

Substances

  • Chelating Agents
  • Iron Chelating Agents
  • Lipoxygenase
  • Prostaglandin-Endoperoxide Synthases