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Diabetes, Vol 49, Issue 3 325-331, Copyright © 2000 by American Diabetes Association
Insulin signaling and insulin sensitivity after exercise in human skeletal muscle
JF Wojtaszewski, BF Hansen, J Gade, B Kiens, JF Markuns, LJ Goodyear and EA Richter
Joslin Diabetes Center, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA. jwojtaszewski@aki.ku.dk
Muscle glucose uptake, glycogen synthase activity, and insulin signaling
were investigated in response to a physiological hyperinsulinemic (600
pmol/l)-euglycemic clamp in young healthy subjects. Four hours before the
clamp, the subjects performed one-legged exercise for 1 h. In the exercised
leg, insulin more rapidly activated glucose uptake (half activation time
[t1/2] = 11 vs. 34 min) and glycogen synthase activity (t1/2 = 8 vs. 17
min), and the magnitude of increase was two- to fourfold higher compared
with the rested leg. However, prior exercise did not result in a greater or
more rapid increase in insulin-induced receptor tyrosine kinase (IRTK)
activity (t1/2 = 50 min), serine phosphorylation of Akt (t1/2 = 1-2 min),
or serine phosphorylation of glycogen synthase kinase-3 (GSK-3) (t1/2 = 1-2
min) or in a larger or more rapid decrease in GSK-3 activity (t1/2 = 3-8
min). Thirty minutes after cessation of insulin infusion, glucose uptake,
glycogen synthase activity, and signaling events were partially reversed in
both the rested and the exercised leg. We conclude the following: 1)
physiological hyperinsulinemia induces sustained activation of
insulin-signaling molecules in human skeletal muscle; 2) the more distal
insulin-signaling components (Akt, GSK-3) are activated much more rapidly
than the proximal signaling molecules (IRTK as well as insulin receptor
substrate 1 and phosphatidylinositol 3-kinase [Wojtaszewski et al.,
Diabetes 46:1775-1781, 1997]); and 3) prior exercise increases insulin
stimulation of both glucose uptake and glycogen synthase activity in the
absence of an upregulation of signaling events in human skeletal muscle.

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Copyright © 2000 by the American Diabetes Association.
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