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The Annals of Thoracic Surgery, Vol 36, 320-327, Copyright © 1983 by The Society of Thoracic Surgeons
VR Conti and RL Kao
The isolated working rat heart model of ischemic arrest was used to
determine if the addition of carbohydrate substrate to our cardioplegic
solution enhanced metabolic and functional myocardial protection. A
single-dose cardioplegia technique, as used in earlier studies that showed
glucose to have a harmful effect, and a multidose technique similar to that
used clinically were studied and compared. Because recent data suggest that
fructose-1,6-diphosphate(FDP) may have a protective effect with ischemia,
this substrate was also tested and compared to glucose and fructose. In
this model, single-dose cardioplegia resulted in poor protection from
ischemic injury in all study groups. There was marked improvement in
myocardial protection with multidose cardioplegia, and further substantial
protection of myocardial function, high-energy phosphate levels, and
glycogen stores when carbohydrate substrate was added to the arrest
solution. The solution with a higher concentration of glucose (0.5%)
provided the best overall metabolic and functional recovery and was clearly
superior to fructose and FDP, both of which had about the same protective
effect. Improved protection with carbohydrate substrate was accompanied by
evidence of substantial increase in glycolytic flux, supporting the idea
that increased anaerobic glycolysis can help protect the ischemic
myocardium when intermittent reinfusion of cardioplegic solution is done.
ARTICLES
Metabolic and functional effects of carbohydrate substrate with single- dose and multiple-dose potassium cardioplegia
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