Lack of the effect of superoxide dismutase and catalase on Na+,K+-ATPase activity in stunned rabbit hearts
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18373391
DOI
10.33549/physiolres.931553
PII: 1553
Knihovny.cz E-resources
- MeSH
- Antioxidants metabolism MeSH
- Time Factors MeSH
- Down-Regulation MeSH
- Ventricular Function, Left MeSH
- Catalase metabolism MeSH
- Ventricular Pressure MeSH
- Myocardial Contraction MeSH
- Rats MeSH
- Myocardium enzymology MeSH
- Oxidation-Reduction MeSH
- Perfusion MeSH
- Myocardial Reperfusion Injury enzymology physiopathology prevention & control MeSH
- Sodium-Potassium-Exchanging ATPase metabolism MeSH
- Sulfhydryl Compounds metabolism MeSH
- Superoxide Dismutase metabolism MeSH
- Myocardial Stunning enzymology physiopathology prevention & control MeSH
- In Vitro Techniques MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antioxidants MeSH
- Catalase MeSH
- Sodium-Potassium-Exchanging ATPase MeSH
- Sulfhydryl Compounds MeSH
- Superoxide Dismutase MeSH
Reactive oxygen species (ROS) have been implicated in the mechanism of postischemic contractile dysfunction, known as myocardial stunning. In this study, we examined protective effects of antioxidant enzymes, superoxide dismutase (SOD) and catalase, against ischemia/reperfusion-induced cardiac dysfunction and inhibition of Na+,K+-ATPase activity. Isolated Langendorff-perfused rabbit hearts were subjected to 15 min of global normothermic ischemia followed by 10 min reperfusion. The hearts treated with SOD plus catalase did not show significant recovery of left ventricular (LV) end-diastolic pressure compared with untreated ischemic reperfused hearts. Treatment with antioxidants had no protective effects on developed LV pressure or its maximal positive and negative first derivatives (+/-LVdP/dt). Myocardial stunning was accompanied by significant loss in sarcolemmal Na+,K+-ATPase activity and thiol group content. Inhibition of enzyme activity and oxidation of SH groups were not prevented by antioxidant enzymes. These results suggest that administration of SOD and catalase in perfusate do not protect significantly against cardiac dysfunction in stunned rabbit myocardium.
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