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The Annals of Thoracic Surgery, Vol 57, 1636-1641, Copyright © 1994 by The Society of Thoracic Surgeons
JM Pearl, J Hiramoto, H Laks, DC Drinkwater Jr and PA Chang
Amino acid enrichment of cardioplegic solutions has been shown to improve
both the metabolic and functional recovery of ischemic myocardium. However,
because of the marked systemic vasodilatation involved, use of amino acid
enrichment is limited to the periods of induction and reperfusion. Fumarate
is a Krebs' cycle intermediate whose conversion to succinate is responsible
for the generation of adenosone triphosphate and the oxidation of the
reduced form of nicotinamide-adenine nucleotide which is the pathway by
which aspartate exerts its effect. Fumarate may also function as a
free-radical scavenger and is involved in calcium transport. To determine
if fumarate-enriched blood cardioplegia would improve the functional
recovery of the neonatal heart, 14 neonatal piglet hearts were isolated and
placed on a blood-perfused working heart circuit. After the baseline
functional and metabolic assessment was done, cold ischemic arrest was
initiated with either standard blood cardioplegic solution (group I; N = 7)
or fumarate-enriched (13 mmol/L) blood cardioplegic solution (group II; N =
7). Cardioplegic solution was given at a pressure of 40 mm Hg every 20
minutes for 2 hours, and topical hypothermia was used. Sixty minutes after
warm whole blood reperfusion, the functional recovery at left atrial
pressures of 3, 6, 9, and 12 mm Hg was 70%, 66%, 66%, and 65%,
respectively, in group I, versus 102%, 106%, 105%, and 109%, respectively,
in group II (p < 0.05). The tissue creatinine phosphate levels after
reperfusion were significantly higher in group II hearts (15.0 +/- 1.2
mumol/g dry heart tissue) than in group I hearts (9.2 +/- 1.9 mumol/g dry
heart tissue), although the adenosine triphosphate levels were not
significantly different.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Fumarate-enriched blood cardioplegia results in complete functional recovery of immature myocardium
Department of Surgery, University of California at Los Angeles Medical Center 90024.
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