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The Journal of Thoracic and Cardiovascular Surgery, Vol 92, 264-271, Copyright © 1986 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
P Menasche, C Grousset, Y Gauduel and A Piwnica
Oxygen-derived free radicals play an important role in the myocardial
injury associated with ischemia and reperfusion. This study was designed to
assess whether the protection afforded by a K+ rich, Mg2+ rich cardioplegic
solution could be enhanced by the addition of free radical scavengers
acting at different levels of the radical generating pathway. Forty
isolated isovolumic rat hearts were divided into five groups (n = 8). Four
groups of hearts were subjected to 90 minutes of normothermic cardioplegic
arrest followed by 45 minutes of reperfusion. Hearts were given an initial
bolus of either unmodified cardioplegic solution or cardioplegic solution
enriched with superoxide dismutase (200,000 U/L) reduced glutathione (0.1
mmol/L), or peroxidase (6,000 U/L). One group of hearts was aerobically
perfused throughout the experimental protocol and served as nonischemic
controls. Based on comparisons of postreperfusion ventricular pressure
development, maximal ventricular dP/dt, left ventricular compliance and
coronary flow, peroxidase-containing cardioplegic solution afforded the
best myocardial protection, with values of these indicators not
significantly different from those of nonischemic perfused control heart.
Glutathione afforded protection slightly inferior to that of peroxidase but
still markedly better than in groups receiving superoxide dismutase or
unmodified cardioplegic solution. This study confirms that cardioplegic
protection can be enhanced by the addition of free radical scavengers, in
particular peroxidase.
ARTICLES
A comparative study of free radical scavengers in cardioplegic solutions. Improved protection with peroxidase
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