H. Bolukoglu et al., METABOLIC-FATE OF GLUCOSE IN REVERSIBLE LOW-FLOW ISCHEMIA OF THE ISOLATED WORKING RAT-HEART, American journal of physiology. Heart and circulatory physiology, 39(3), 1996, pp. 817-826
The acute adaptation of myocardial glucose metabolism in response to l
ow-flow ischemia and reperfusion was investigated in isolated working
rat hearts perfused with bicarbonate saline containing glucose (10 mM)
and insulin (40 mu U/ml). Reversible low-flow ischemia was induced by
reducing coronary perfusion pressure from 100 to 35 cmH(2)O. Tritiate
d glucose was used to assess rates of glucose transport and phosphoryl
ation, flux from glucose to pyruvate, and oxidation of exogenous gluco
se. Rates of glycogen synthesis and glycolysis were also assessed. Wit
h ischemia, cardiac power decreased by more than two-thirds. Rates of
glucose uptake and flux from glucose to pyruvate remained unchanged, w
hile glucose oxidation declined by 61%. Rates of lactate release more
than doubled, and fractional enrichment of glycogen remained the same.
During reperfusion, glucose oxidation returned to the preischemic val
ues. When isoproterenol was added during ischemia, glucose uptake incr
eased, glycogen decreased, and lactate release increased. No effect wa
s seen with pacing. We conclude that during low-flow ischemia and with
glucose as the only exogenous substrate, net glucose uptake remains u
nchanged. There is a reversible redirection between glycolysis and glu
cose oxidation, while glycogen synthesis continues during ischemia and
is enhanced with reperfusion.