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1 Department of Physiology and Pharmacology, Loma Linda University, Loma Linda 92350; and 2 Division of Physiology, Department of Medicine, University of California, San Diego, La Jolla, California 92093-0623
Gene expression of
vascular endothelial growth factor (VEGF), and to a lesser extent of
transforming growth factor-
1 (TGF-
1) and
basic fibroblast growth factor (bFGF), has been found to increase in
rat skeletal muscle after a single exercise bout. In addition, acute
hypoxia augments the VEGF mRNA response to exercise, which suggests
that, if VEGF is important in muscle angiogenesis, hypoxic training
might produce greater capillary growth than normoxic training.
Therefore, we examined the effects of exercise training (treadmill
running at the same absolute intensity) in normoxia and hypoxia
(inspired O2 fraction = 0.12) on rat skeletal muscle capillarity and on resting and postexercise gene expression of VEGF,
its major receptors (flt-1 and flk-1),
TGF-
1, and bFGF. Normoxic training did not alter
basal or exercise-induced VEGF mRNA levels but produced a modest
twofold increase in bFGF mRNA (P < 0.05). Rats trained
in hypoxia exhibited an attenuated VEGF mRNA response to exercise
(1.8-fold compared 3.4-fold with normoxic training; P < 0.05), absent TGF-
1 and flt-1 mRNA responses to exercise, and an approximately threefold (P < 0.05)
decrease in bFGF mRNA levels. flk-1 mRNA levels were not
significantly altered by either normoxic or hypoxic training. An
increase in skeletal muscle capillarity was observed only in
hypoxically trained rats. These data show that, whereas training in
hypoxia potentiates the adaptive angiogenic response of skeletal muscle
to a given absolute intensity of exercise, this was not evident in the
gene expression of VEGF or its receptors when assessed at the end of training.
Northern blot analysis; angiogenesis; transforming growth
factor-
1; basic fibroblast growth factor; flt-1; flk-1
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