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Cardiovascular Research Group, Departments of 1 Pharmacology and 2 Pediatrics, Faculty of Medicine, University of Alberta, Edmonton, Alberta, Canada T6G 2H7
Glycogen and its
turnover are important components of myocardial glucose metabolism that
significantly impact on postischemic recovery. We developed a method to
measure glycogen turnover (rates of glycogen synthesis and degradation)
in isolated working rat hearts using
[3H]- and
[14C]glucose. In
aerobic hearts perfused with 11 mM glucose, 1.2 mM palmitate, and 100 µU/ml insulin, rates of glycogen synthesis and degradation were 1.24 ± 0.3 and 0.53 ± 0.25 µmol · min
1 · g
dry wt
1, respectively.
Low-flow ischemia (0.5 ml/min, 60 min) elicited a marked
glycogenolysis; rates of glycogen synthesis and degradation were 0.54 ± 0.16 and 2.12 ± 0.14 µmol · min
1 · g
dry wt
1, respectively.
During reperfusion (30 min), mechanical function recovered to 20% of
preischemic values. Rates of synthesis and degradation were 1.66 ± 0.16 and 1.55 ± 0.21 µmol · min
1 · g
dry wt
1, respectively, and
glycogen content remained unchanged (25 ± 3 µmol/g dry wt). The
assessment of glycogen metabolism needs to take into account the
simultaneous synthesis and degradation of glycogen. With this approach,
a substantial turnover of glycogen was detectable not only during
aerobic conditions but also during ischemia as well as reperfusion.
myocardial energy metabolism; left ventricular work; reperfusion injury; glucose oxidation; glycolysis; proton production
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