Myocardial and endothelial dysfunction after multiple, brief coronary occlusions: role of oxygen radicals
G. J. Gross, S. T. O'Rourke, L. R. Pelc and D. C. Warltier Department of Anesthesiology, Medical College of Wisconsin, Milwaukee 53226. The major objective of the present study was to determine the effect of multiple, brief periods of coronary artery occlusion and reperfusion on postischemic co...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1992-12, Vol.263 (6), p.H1703-H1709 |
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Zusammenfassung: | G. J. Gross, S. T. O'Rourke, L. R. Pelc and D. C. Warltier
Department of Anesthesiology, Medical College of Wisconsin, Milwaukee 53226.
The major objective of the present study was to determine the effect of
multiple, brief periods of coronary artery occlusion and reperfusion on
postischemic contractile function (sonomicrometry) and
endothelium-dependent vasodilator responses in isolated conduit coronary
artery rings obtained from anesthetized dogs. The role of oxygen-derived
free radicals was also investigated. Dogs were subjected to four 5-min
episodes of left anterior descending coronary occlusion interspersed with 5
min of reperfusion followed by a final 60-min reperfusion period. The
multiple occlusion-reperfusion protocol resulted in regional segment
dysfunction (37 +/- 15% of preocclusion values at 60 min of reperfusion)
and attenuated endothelium-dependent responses to acetylcholine,
bradykinin, and the calcium ionophore, A23187. Responses to the
endothelium-independent vasodilator, sodium nitroprusside, were unaffected.
Infusion of superoxide dismutase (5,000 U/kg) and catalase (55,000 U/kg)
markedly improved the recovery of myocardial function at 30 and 60 min of
reperfusion and completely protected against vascular endothelial damage.
These results suggest an important role for oxygen-derived free radicals in
the myocardial and endothelial injury that occurs in this model of multiple
stunned myocardium. |
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ISSN: | 0363-6135 0002-9513 1522-1539 |
DOI: | 10.1152/ajpheart.1992.263.6.h1703 |