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
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Animals
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Coordination Complexes
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Coronary Circulation / drug effects
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Creatine Kinase / metabolism
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Free Radical Scavengers*
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Hemodynamics / drug effects
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In Vitro Techniques
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Male
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Myocardial Ischemia / drug therapy
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Myocardial Ischemia / physiopathology*
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Myocardial Reperfusion Injury / drug therapy
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Myocardial Reperfusion Injury / physiopathology*
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Myocardium / enzymology
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Organometallic Compounds / pharmacology*
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Rats
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Rats, Wistar
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Superoxide Dismutase / pharmacology*
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Superoxides / toxicity
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Thiobarbituric Acid Reactive Substances / metabolism
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Thiosemicarbazones / pharmacology*
Substances
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Coordination Complexes
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Free Radical Scavengers
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Organometallic Compounds
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Thiobarbituric Acid Reactive Substances
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Thiosemicarbazones
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copper (II) diacetyl-di(N(4)-methylthiosemicarbazone)
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Superoxides
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Superoxide Dismutase
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Creatine Kinase