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-Adrenergic blockade augments glucose utilization in horses
during graded exercise
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus, Ohio 43210
To examine the role of
-adrenergic
mechanisms in the regulation of endogenous glucose (Glu) production
[rate of appearance (Ra)] and utilization [rate of
disappearance (Rd)] and carbohydrate (CHO) metabolism, six
horses completed consecutive 30-min bouts of exercise at ~30% (Lo)
and ~60% (Hi) of estimated maximum O2 uptake with (P)
and without (C) prior administration of the
-blocker propranolol
(0.22 mg/kg iv). All horses completed exercise in C; exercise duration
in P was 49.9 ± 1.2 (SE) min. Plasma Glu was unchanged in C
during Lo but increased progressively in Hi. In P, plasma Glu rose
steadily during Lo and Hi and was higher (P < 0.05)
than in C throughout exercise. Plasma insulin declined during exercise
in P but not in C;
-blockade attenuated (P < 0.05)
the rise in plasma glucagon and free fatty acids and exaggerated the
increases in epinephrine and norepinephrine. Glu Ra was
8.1 ± 0.8 and 8.4 ± 1.0 µmol · kg
1 · min
1 at rest
and 30.5 ± 3.6 and 42.8 ± 4.1 µmol · kg
1 · min
1 at the
end of Lo in C and P, respectively. During Hi, Glu Ra increased to 54.4 ± 4.4 and 73.8 ± 4.7 µmol · kg
1 · min
1 in C
and P, respectively. Similarly, Glu Rd was ~40% higher
in P than in C during Lo (27.3 ± 2.0 and 39.5 ± 3.3 µmol · kg
1 · min
1 in C
and P, respectively) and Hi (37.4 ± 2.6 and 61.5 ± 5.3 µmol · kg
1 · min
1 in C
and P, respectively).
-Blockade augmented CHO oxidation (CHOox) with a concomitant reduction in fat oxidation.
Inasmuch as estimated muscle glycogen utilization was similar between
trials, the increase in CHOox in P was due to increased use
of plasma Glu. We conclude that
-blockade increases Glu
Ra and Rd and CHOox in horses
during exercise. The increase in Glu Rd under
-blockade suggests that
-adrenergic mechanisms restrain Glu Rd
during exercise.
stable isotopes; carbohydrate oxidation; propranolol; insulin; glucagon; catecholamines
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