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Exercise Physiology and Metabolism Laboratory, Department of Kinesiology and Health Education, University of Texas at Austin, Austin, Texas 78712
The present study was conducted to determine the effect of
chronic administration of the long-acting
2-adrenergic
agonist clenbuterol on rats that are genetically prone to insulin
resistance and impaired glucose tolerance. Obese Zucker rats
(fa/fa) were given 1 mg/kg of clenbuterol by oral intubation
daily for 5 wk. Controls received an equivalent volume of water
according to the same schedule. At the end of the treatment, rats were
catheterized for euglycemic-hyperinsulinemic (15 mU
insulin · kg
1 · min
1)
clamping. Clenbuterol did not change body weight compared with the
control group but caused a redistribution of body weight: leg muscle
weights increased, and abdominal fat weight decreased. The glucose
infusion rate needed to maintain euglycemia and the rate of
glucose disappearance were greater in the clenbuterol-treated rats.
Furthermore, plasma insulin levels were decreased, and the rate of
glucose uptake into hindlimb muscles and abdominal fat was increased in
the clenbuterol-treated rats. This increased rate of glucose uptake was
accompanied by a parallel increase in the rate of glycogen synthesis.
The increase in muscle glucose uptake could not be ascribed to an
increase in the glucose transport protein GLUT-4 in clenbuterol-treated
rats. We conclude that chronic clenbuterol treatment reduces the
insulin resistance of the obese Zucker rat by increasing
insulin-stimulated muscle and adipose tissue glucose uptake. The
improvements noted may be related to the repartitioning of body weight
between tissues.
skeletal muscle; glucose uptake; glycogen; triacylglycerol; adipose tissue; euglycemic-hyperinsulinemic clamp
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