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Department of Physiology, The University of Melbourne, Parkville, Victoria 3010, Australia
This study examined the roles of the
female sex steroids, 17
-estradiol (E2) and progesterone
(Prog), on glucose uptake and GLUT4 protein expression. Female
Sprague-Dawley rats were either sham operated (C) or ovariectomized and
treated with placebo (O), E2 (E), Prog (P), or both
hormones at physiological doses (P + E) or the same dose of Prog with
a high dose of E2 (P + HiE) via timed-release pellets
inserted at the time of surgery, 15 days before metabolic testing. On
the morning of day 15, animals received a 300-µCi
injection (ip) of 2-deoxy-[14C]glucose and then either
exercised on a motorized treadmill for 30 min at 0.35 m/s or remained
sedentary in their cages for the same period. Basal glucose uptake was
not different between the treatment groups in either the red or white
quadriceps. However, glucose uptake was decreased (P < 0.05) in O, P, and P + E rats during exercise in the red quadriceps
compared with C rats, whereas E and P + HiE treatment restored
glucose uptake. Glycogen content in skeletal muscle followed similar
trends, with no differences seen in resting animals. Postexercise red
quadriceps glycogen levels were higher (P < 0.05) in
the E and P + HiE rats compared with O and P. Treatment of
ovariectomized rats with progesterone (P rats) decreased
(P < 0.05) GLUT4 content in the red quadriceps by 21%
compared with C rats. These data demonstrate that estrogen-deficient animals have a decreased ability for contraction-stimulated glucose uptake and increased glycogen use during aerobic exercise. However, changes in contraction-stimulated glucose uptake could not be explained
by altered transporter protein content, since the absence of
E2 had no effect on GLUT4 protein.
ovariectomy; estrogen; progesterone; carbohydrate metabolism
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