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1 Laboratoire de la Performance Motrice, Université Blaise Pascal, Clermont-Ferrand; and 2 Unité Maladies Métaboliques et Micronutriments, INRA Clermont-Theix, 63177 Aubière, France
This paper reports
that the selective
2-adrenergic receptor agonist
clenbuterol affects bone metabolism in growing 3-mo-old male Wistar
rats treated over 8 wk. Thirty-two 3-mo-old growing Wistar rats
weighing 234 ± 2 g were assigned to a progressive isometric
force, strength-training exercise program plus oral clenbuterol (2 mg · kg body wt
1 · day
1)
for 5 days each week, exercise program without clenbuterol 5 days each
week, no exercise program plus oral clenbuterol (2 mg · kg
1 · day
1) for 5 days
each week, or no exercise without clenbuterol 5 days each week. At the
end of 8 wk, lean mass, fat mass, and right total femoral, distal
metaphyseal femoral, and diaphyseal femoral bone mineral density were
measured by Hologic QDR 4500 dual X-ray absorptiometry (DEXA)
technique. Left femoral bones were harvested after death on day
58, and femoral resistance was determined by three-point bending
testing. We found that fat mass was decreased in rats given strength
training exercise and decreased further in rats treated with
clenbuterol. Lean mass was increased in clenbuterol-treated animals.
Strength-training exercise appeared to have no effect on bone mineral
density, serum osteocalcin, or urinary deoxypyridinoline. However,
clenbuterol treatment decreased femoral length, diameter, bone mineral
density, and mechanical resistance. Clenbuterol had no effect on
osteocalcin but increased urinary deoxypyridinoline. We concluded that
clenbuterol treatment decreased bone mineral density and increased bone
resorption independent of the level of exercise rats were given.
strength training; bone mineral density; osteocalcine; deoxypyridinoline
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