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The Annals of Thoracic Surgery, Vol 53, 412-418, Copyright © 1992 by The Society of Thoracic Surgeons
DA DeBoer and RE Clark
Oxygen-derived free radicals have been implicated in myocardial
ischemia-reperfusion injury. It has been proposed that deferoxamine, an
iron chelator, improves myocardial preservation by reducing the iron-
catalyzed production of the hydroxyl radical. The objectives of this study
were to define the appropriate timing of iron chelation therapy and the
dose-response properties of deferoxamine. Isolated working rat hearts were
subjected to 25 minutes of normothermic global ischemia. Deferoxamine was
given as pretreatment (n = 39; doses of 10 or 30 mg/kg), added to
cardioplegic solution (n = 43; doses 0.46 to 1.90 mmol/L), or administered
upon reperfusion (n = 52; doses 0.15 to 0.76 mmol/L) and compared with
saline controls (n = 25). Deferoxamine pretreatment improved survival at
each dose from a control value of 44% to 71% and 72% (p less than 0.05),
respectively. A cardioplegia dose of 0.46 mmol/L improved survival from 48%
to 75%. Higher doses reduced survival and implied a toxic effect.
Reperfusion therapy did not alter survival. Regardless of time of
administration, deferoxamine did not improve ventricular function or
adenosine triphosphate levels. Deferoxamine given as pretreatment 1 hour
before ischemia at doses of 30 mg/kg, and perhaps as low as 10 mg/kg,
significantly improved survival. The addition of deferoxamine to
cardioplegic solution was safe and may be protective at approximately 0.50
mmol/L; however, toxicity should be considered at concentrations greater
than 0.76 mmol/L. These data support the postulate that iron catalysis is
involved in the production of oxygen-derived free radicals during
ischemia-reperfusion injury. We conclude that pretreatment before ischemia
is an important component of iron chelation therapy in myocardial
preservation.
ARTICLES
Iron chelation in myocardial preservation after ischemia-reperfusion injury: the importance of pretreatment and toxicity
Surgery Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.
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