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Am J Physiol Heart Circ Physiol 275: H1533-H1541, 1998;
0363-6135/98 $5.00
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Vol. 275, Issue 5, H1533-H1541, November 1998

Assessment of glycogen turnover in aerobic, ischemic, and reperfused working rat hearts

Heather Fraser1, Gary D. Lopaschuk1,2, and Alexander S. Clanachan1

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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