Ac. Hackney et al., The effect of sex steroid hormones on substrate oxidation during prolongedsubmaximal exercise in women, JPN J PHYSL, 50(5), 2000, pp. 489-494
In animals, female sex steroid hormones (SS, estrogens-progesterone) influe
nce the energy substrate that is metabolized. Human research on this issue
is controversial. This study examined whether changes in circulating SS hor
mone levels affected the carbohydrate-lipid metabolism during submaximal pr
olonged (60 min) exercise. Young, physically active females were studied, F
our were classified as anovulatory-oligomenorrheic and four were classified
as ovulatory-eumenorrheic. Subject responses were pooled to form one group
(n=8) and then their responses under low (L) and high (H) pharmaceutically
manipulated SS hormone conditions were examined. During exercise, the mean
oxygen consumption levels were 1.70+/-0.10/.min(-1) for L-SS and 1.75+/-0.
11/.min(-1) for H-SS (p= 0.07), respectively. The respiratory exchange rati
o (RER) responses were significantly different during exercise between the
conditions: 0.93+/-0.04 for L-SS and 0.90+/-0.04 for H-SS (p<0.05), respect
ively. RER responses were utilized to calculate substrate oxidation. Signif
icantly less carbohydrate oxidation was found in the H-SS condition as comp
ared to the L-SS condition (p<0.05). Lipid oxidation was also significantly
different, but for this measure, the levels of oxidation were greater in t
he H-SS than in the L-SS condition (p<0.05). Finally, total energy expendit
ure for the 60 min of exercise was not significantly different between the
hormonal conditions. Results suggest that sex steroid hormones have an impa
ct upon substrate oxidation in women during exercise. Specifically, high ci
rculating concentrations of the SS hormones result in an enhanced reliance
upon the oxidation of lipid as an energy substrate and consequently induce
a reduction in carbohydrate oxidation. The mechanism inducing this "metabol
ism shift" appears due to sex steroid hormones directly and indirectly incr
easing lipid mobilization and lipolysis.