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The Journal of Thoracic and Cardiovascular Surgery, Vol 105, 995-1006, Copyright © 1993 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
P Owen, EF du Toit and LH Opie
The purpose of this study was to determine the mechanisms by which high
physiologic concentrations of glucose (11 mmol/L) were protective while
even higher concentrations (20 or 50 mmol/L) were harmful when added to St.
Thomas' Hospital No. 2 cardioplegic solution. We evaluated the recovery of
isolated working rat hearts subjected to 3 hours of hypothermic multidose
cardioplegic arrest. The addition of glucose 11 mmol/L was associated with
better aortic flow (79.2% +/- 1.3%) than the addition of glucose 1 mmol/L
(61.7% +/- 2.7%), 20 mmol/L (73.6% +/- 1.1%), or 50 mmol/L (66.0% +/- 3.2%)
(p < 0.01 versus glucose 1 and 50 mmol/L). An increase in glucose
concentration from 1 to 50 mmol/L progressively augmented glucose flux from
2.2 +/- 0.33 to 10.4 +/- 0.79 mumol/gm per 3 hours (p < 0.01), but
higher glucose concentrations of 20 and 50 mmol/L inhibited glycogenolysis
(p < 0.05 versus glucose 1 and 11 mmol/L), so that total glycolysis was
decreased and consequently glycolytic adenosine triphosphate production was
reduced from 35.9 +/- 0.47 (glucose 11 mmol/L) to 27.5 +/- 1.25 mumol/gm
per 3 hours (glucose 50 mmol/L) (p < 0.01). The end products of
glycolysis (lactate and protons) did not appear to affect the recovery of
the hearts, because both lactate efflux and tissue lactate were highest in
the presence of glucose 11 mmol/L and the pH of the cardioplegic effluent
was more alkalotic in glucose 11 and 20 mmol/L. Thus a high physiologic
concentration of glucose (11 mmol/L) in the cardioplegic solution improved
recovery because of an increased glycolytic adenosine triphosphate
production during cardioplegic arrest, whereas even higher concentrations
of glucose inhibited these effects.
ARTICLES
The optimal glucose concentration for intermittent cardioplegia in isolated rat heart when added to St. Thomas' Hospital cardioplegic solution
Department of Medicine, Groote Schuur Hospital, Cape Town, South Africa.
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