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Departments of Medicine, Molecular Physiology, and Biophysics, Vanderbilt University School of Medicine, and Nashville Veterans Administration/Juvenile Diabetes Foundation Diabetes Research Center, Nashville, Tennessee 37232
Address all correspondence and requests for reprints to: Stephen N. Davis, M.D., Division of Diabetes and Endocrinology, 712 MRB II, Vanderbilt University School of Medicine, Nashville, Tennessee 37232. E-mail: steve.davis{at}mcmail.vanderbilt.edu
Significant, sexual dimorphisms exist in counterregulatory responses to
commonly occurring stresses, such as hypoglycemia, fasting, and
cognitive testing. The question of whether counterregulatory responses
differ during exercise in healthy men and women remains controversial.
The aim of this study was to determine whether a sexual dimorphism
exists in neuroendocrine, metabolic, or cardiovascular responses to
prolonged moderate exercise. Sixteen healthy (eight men and eight
women) subjects matched for age (28 ± 2 yr), body mass index
(22 ± 1 kg/m2), nutrient intake, and spectrum of
physical fitness were studied in a randomized fashion during 90 min of
exercise on a cycle ergometer at 80% of their anaerobic threshold
(
50% VO2 max). Respiratory quotient and oxygen
consumption relative to body weight were identical in men and women.
Glycemia was equated (5.3 ± 0.2 mmol/L) during exercise via an
exogenous glucose infusion. Gender had significant effects on
counterregulatory responses during exercise. Arterialized epinephrine
(1.05 ± 0.2 vs. 0.45 ± 0.04 nmol/L),
norepinephrine (9.2 ± 1.1 vs. 5.8 ± 1.1
nmol/L), and pancreatic polypeptide (52 ± 6 vs.
37 ± 6 pmol/L) were significantly (P < 0.01)
increased in men compared to women, respectively. Plasma glucagon,
cortisol, and GH levels responded similarly in men and women. Insulin
values were higher at baseline in men and fell by a greater amount to
reach similar levels during exercise compared to those in women.
Endogenous glucose production, measured with
[3-3H]glucose was similar in men and women. Carbohydrate
oxidation was significantly increased in men relative to women
(21.2 ± 2 vs. 15.6 ± 2 mg/kg fat free
mass·min; P < 0.05). Despite reduced sympathetic
nervous system (SNS) drive, lipolytic responses were increased in
women. Arterialized blood glycerol (215 ± 30 vs.
140 ± 20 µmol/L), ß-hydroxybutyrate (54 ± 9
vs. 25 ± 10 µmol/L), and plasma nonesterified
fatty acids (720 ± 56 vs. 469 ± 103
µmol/L) were significantly (P < 0.01) increased
in women. In keeping with increased SNS activity, systolic blood
pressure and mean arterial pressure were significantly increased
(P < 0.01) in men.
In summary, this study demonstrates that a significant sexual dimorphism exists in neuroendocrine, metabolic, and cardiovascular counterregulatory responses to prolonged moderate exercise in man. We conclude that during exercise, men have increased autonomic nervous system (epinephrine, norepinephrine, pancreatic polypeptide), cardiovascular (systolic, mean arterial pressure) and certain metabolic (carbohydrate oxidation) counterregulatory responses, but that women have increased lipolytic (glycerol, nonesterified fatty acids) and ketogenic (ß-hydroxybutyrate) responses. Women may compensate for diminished SNS activity during exercise by increased lipolytic responses.
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