Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Evidence for a pathogenic role of xanthine oxidase in the stunned myocardium

Journal Article · · Am. J. Physiol.; (United States)
OSTI ID:5993911
Recent evidence suggests that postischemic myocardial dysfunction (or myocardial stunning) may be mediated by oxygen free radicals, but the mechanism for their production remains unknown. To explore the role of xanthine oxidase as a potential source of free radicals, open-chest dogs undergoing a 15-min occlusion of the left anterior descending coronary artery (LAD) followed by 4 h of reperfusion (REP) received intravenously either allopurinol or saline. The two groups were similar with respect to occluded bed size (postmortem perfusion) and collateral flow (radioactive microspheres). In controls, the transcardiac difference in plasma uric acid increased 199 +/- 70% (means +/- SE) during ischemia and remained elevated for 5 min after REP; no increase was observed in treated dogs. Regional myocardial function was assessed by measuring systolic wall thickening with an epicardial Doppler probe. The two groups exhibited comparable systolic thickening under base-line conditions and similar degrees of dyskinesis during ischemia. Following REP, however, recovery of contractile function (expressed as percent of preocclusion values) was considerably greater in allopurinol-treated as compared with control dogs. These differences could not be ascribed to hemodynamic factors. The results suggest that xanthine oxidase is a source of the oxygen free radicals responsible for myocardial stunning following a brief episode of reversible regional ischemia.
Research Organization:
Baylor College of Medicine, Houston, TX
OSTI ID:
5993911
Journal Information:
Am. J. Physiol.; (United States), Journal Name: Am. J. Physiol.; (United States) Vol. 252:3; ISSN AJPHA
Country of Publication:
United States
Language:
English