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The Annals of Thoracic Surgery, Vol 47, 663-668, Copyright © 1989 by The Society of Thoracic Surgeons
GK Lofland, AS Abd-Elfattah, R Wyse, M de Leval, J Stark and AS Wechsler
Quantitative assessment of high-energy phosphate levels, including
degradation or utilization during ischemia, has not previously been
performed in infants and children. Animal experiments suggest that high-
energy phosphate metabolism varies with maturation. To help answer these
questions, 24 patients aged 2 months to 8 years underwent myocardial biopsy
immediately after the institution of cardiopulmonary bypass (16 to 20
degrees C). Additional samples were obtained at 16 and 45 minutes after
aortic cross-clamping and administration of cardioplegia (St. Thomas's
solution) (in vivo ischemia). Seven patients also underwent major
myocardial resection. Resected specimens were placed in a 37 degrees C bath
and divided into equal-sized samples that were removed at ten-minute
intervals (in vitro ischemia). All samples were immersed in liquid nitrogen
and analyzed for adenine nucleotide pool metabolites using high-performance
liquid chromatography. Levels of adenosine triphosphate were high before
cross-clamping but diminished during the period of protected ischemia.
Adenosine triphosphate loss was much more pronounced in patients less than
18 months old (p less than 0.05) and was associated with accumulation of
adenosine monophosphate and inosine, a finding not seen in patients more
than 18 months old (p less than 0.05). The same trends documented during in
vivo ischemia were noted during in vitro ischemia. Immaturity of
5'-nucleotidase results in accumulation of adenosine monophosphate during
ischemia. It is known that 5'-nucleotidase is present in neonatal
myocardial cell membranes and absent from the cytosol.(ABSTRACT TRUNCATED
AT 250 WORDS)
ARTICLES
Myocardial adenine nucleotide metabolism in pediatric patients during hypothermic cardioplegic arrest and normothermic ischemia
Cardiothoracic Unit, Hospital for Sick Children, London, England.
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