Cu-ATSM, an intracellular-accessible superoxide dismutase (SOD)-like copper complex: evaluation in an ischemia-reperfusion injury model

Biol Pharm Bull. 1994 May;17(5):701-4. doi: 10.1248/bpb.17.701.

Abstract

We have reported a stable superoxide dismutase (SOD)-like copper complex, Cu-ATSM, which shows high membrane permeability and distribution to the brain or heart. In this study, we evaluated the protective effects of Cu-ATSM on superoxide-mediated tissue damage caused by ischemia-reperfusion using an isolated perfused rat heart model. Lipid peroxidation levels in the Cu-ATSM treated group were lower than those in the non-treated group. Furthermore, released creatine phosphokinase into the perfusate, a marker of tissue damage, was reduced by Cu-ATSM treatment. These results indicated the possibility of Cu-ATSM being an effective SOD-like drug for the treatment of superoxide-mediated damage, such as ischemia-reperfusion injury.

MeSH terms

  • Animals
  • Coordination Complexes
  • Coronary Circulation / drug effects
  • Creatine Kinase / metabolism
  • Free Radical Scavengers*
  • Hemodynamics / drug effects
  • In Vitro Techniques
  • Male
  • Myocardial Ischemia / drug therapy
  • Myocardial Ischemia / physiopathology*
  • Myocardial Reperfusion Injury / drug therapy
  • Myocardial Reperfusion Injury / physiopathology*
  • Myocardium / enzymology
  • Organometallic Compounds / pharmacology*
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase / pharmacology*
  • Superoxides / toxicity
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Thiosemicarbazones / pharmacology*

Substances

  • Coordination Complexes
  • Free Radical Scavengers
  • Organometallic Compounds
  • Thiobarbituric Acid Reactive Substances
  • Thiosemicarbazones
  • copper (II) diacetyl-di(N(4)-methylthiosemicarbazone)
  • Superoxides
  • Superoxide Dismutase
  • Creatine Kinase