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Other Original Studies |
Division of Endocrinology and Metabolism, Department of Medicine (J.A.K., A.W., M.L.H.); Division of Biostatistics and Epidemiology, Department of Health Evaluation Sciences (K.S.P.); Department of Human Services (A.W.); General Clinical Research Center (J.Y.W., A.W.); and the National Science Foundation Center for Biological Timing (M.L.H.), University of Virginia, Charlottesville, Virginia 22908
Address all correspondence and requests for reprints to: Dr. Mark L. Hartman, Eli Lilly and Co., Lilly Corporate Center, Drop Code 5015, Indianapolis, Indiana 46285.
Abstract
Exercise of appropriate intensity is a potent stimulus for GH and
cortisol secretion. Circadian and diurnal rhythms may modulate the GH
and cortisol responses to exercise, but nutrition, sleep, prior
exercise patterns, and body composition are potentially confounding
factors. To determine the influence of the time of day on the GH and
cortisol response to acute exercise, we studied 10 moderately trained
young men (24.1 ± 1.1 yr old; maximal oxygen consumption,
47.9 ± 1.4 mL/kg·min; percent body fat, 13.2 ± 0.6%).
After a supervised night of sleep and a standard meal 12 h before
exercise, subjects exercised at a constant velocity (to elicit an
initial blood lactate concentration of
2.5 mmol/L) on a treadmill
for 30 min on 3 separate occasions, starting at 0700, 1900, and
2400 h. Blood samples were obtained at 5-min intervals for 1
h before and 5 h after the start of exercise; subjects were not
allowed to sleep during this period. Subjects were also studied on 3
control days under identical conditions without exercise. There were no
significant differences with time of day in the mean blood lactate and
submaximal oxygen consumption values during exercise. The differences
over time in serum GH and cortisol concentrations between the exercise
day and the control day were determined with 95% confidence limits for
each time of day. Exercise stimulated a significant increase in serum
GH concentrations over control day values for approximately 105145
min (P < 0.05) with no significant difference in
the magnitude of this response by time of day. The increase in serum GH
concentrations with exercise was followed by a transient suppression of
GH release (for
5590 min; P < 0.05) after
exercise at 0700 and 1900 h, but not at 2400 h. Although the
duration of the increase in serum cortisol concentrations after
exercise was similar (
150155 min; P < 0.05)
at 0700, 1900, and 2400 h, the magnitude of this increase over
control day levels was greatest at 2400 h. This difference was
significant for approximately 130 min and approximately 40 min compared
to exercise at 1900 and 0700 h, respectively
(P < 0.05). The cortisol response to exercise at
0700 h was significantly greater than that at 1900 h for
about 55 min (P < 0.05). A rebound suppression of
cortisol release for about 50 min (P < 0.05) was
observed after exercise at 2400 h, but not 0700 or 1900 h.
Both baseline (before exercise) and peak cortisol concentrations were
significantly higher at 0700 h than at 1900 or 2400 h
(P < 0.01). We conclude that time of day does not
alter the GH response to exercise; however, the exercise-induced
cortisol response is modulated by time of day.
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