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Obesity and Diabetes Research Center, Department of Physiology, School of Medicine, University of Maryland, Baltimore, Maryland 21201
It is well known
that an alteration in insulin activation of skeletal muscle glycogen
synthase is associated with insulin resistance. To determine whether
this defect in insulin action is specific to skeletal muscle, or also
present in liver, simultaneous biopsies of these tissues were obtained
before and during a euglycemic hyperinsulinemic clamp in spontaneously
obese insulin-resistant male rhesus monkeys. The activities of glycogen
synthase and glycogen phosphorylase and the concentrations of glucose
6-phosphate and glycogen were measured. There were no differences
between basal and insulin-stimulated glycogen synthase and glycogen
phosphorylase activities or in glucose 6-phosphate and glycogen
contents in muscle. Insulin increased the activities of liver glycogen
synthase (P < 0.05) and decreased
the activities of liver glycogen phosphorylase (P
0.001). Insulin also caused a
reduction in liver glucose 6-phosphate
(P = 0.05). We conclude that
insulin-resistant monkeys do not have a defect in insulin action on
liver glycogen synthase, although a defect in insulin action on muscle
glycogen synthase is present. Therefore, tissue-specific alterations in
insulin action on glycogen synthase are present in the development of insulin resistance in rhesus monkeys.
glucose 6-phosphate; whole body insulin-mediated glucose disposal rate; skeletal muscle; adipose tissue
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