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The Journal of Thoracic and Cardiovascular Surgery, Vol 102, 297-308, Copyright © 1991 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
W Ko, AS Hawes, WD Lazenby, SE Calvano, YT Shin, JA Zelano, AC Antonacci, OW Isom and KH Krieger
To study the roles of platelet-activating factor, polymorphonuclear
leukocytes, and oxygen free radicals in myocardial reperfusion injury, we
subjected 10 sheep to 90 minutes of mid-left anterior descending coronary
artery followed by 6 hours of reperfusion. Stainings with gentian violet
and tetratriphenyl ammonium chloride demonstrated 20% +/- 3% of the left
ventricular mass at risk for ischemia, of which 75% +/- 10% underwent
infarction. Coronary sinus blood was assayed for platelet- activating
factor and neutrophil hydrogen peroxide production before and during
coronary occlusion and during reperfusion. Platelet- activating factor was
isolated by column chromatography and lipid extraction and quantified by
radioimmunoassay. Neutrophil hydrogen peroxide production was measured by a
2',7'-dichlorofluorescein flow- cytometric assay. Platelet-activating
factor was elevated to 899 +/- 210 pg/ml at 15 minutes of reperfusion,
compared with the preocclusion level of 271 +/- 55 pg/ml and coronary
occlusion level of 359 +/- 64 pg/ml (p less than 0.05; analysis of
variance). Neutrophil hydrogen peroxide production, measured on a relative
fluorescence scale, was also elevated to a level of 141 +/- 27 at 1 hour of
reperfusion, compared with the preocclusion level of 103 +/- 6 and the
coronary occlusion level of 114 +/- 13 (p less than 0.01; analysis of
variance). Both of these parameters returned toward baselines at the end of
6 hours of reperfusion. Histologic examination revealed infiltration of
polymorphonuclear leukocytes into the interstitium of the reperfused
myocardium. Neutrophils isolated from unoperated and healthy sheep
demonstrated a graded dose response in hydrogen peroxide production when
stimulated by purified platelet-activating factor in vitro. These findings
suggest that platelet-activating factor is released in the coronary
circulation and is a mediator of oxygen free radical production in
polymorphonuclear leukocytes during myocardial reperfusion.
ARTICLES
Myocardial reperfusion injury. Platelet-activating factor stimulates polymorphonuclear leukocyte hydrogen peroxide production during myocardial reperfusion
Department of Surgery, New York Hospital-Cornell University Medical College, NY 10021.
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