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Submitted on April 28, 2005
Accepted on August 16, 2005
-estradiol supplementation decreases glucose Ra and Rd with no effect on glycogen utilization during moderate intensity exercise in men
Departments of Pediatrics and Medicine, McMaster University, Hamilton, ON; Department of Human Biology and Nutritional Sciences, University of Guelph, Guelph, ON
* To whom correspondence should be addressed. E-mail: tarnopol{at}mcmaster.ca.
Context and Objective: Women use less carbohydrate during endurance exercise, as compared with men. In rodents, 17-
-estradiol (E2) supplementation robustly increases lipid use and lowers muscle and liver glycogen use during exercise. E2 supplementation has been found to influence substrate selection by decreasing glucose rate of appearance (Ra), disappearance (Rd) and metabolic clearance rate (MCR) during exercise in humans; however, neither a change in total carbohydrate use nor a sparing of muscle glycogen were demonstrated.
Subjects and Methods: We investigated the effect of 8 days of E2 (17-
-estradiol, 2 mg/d) supplementation on glucose turnover and net muscle glycogen use in 11 men using a randomized, double blind, placebo controlled, cross-over design. Subjects underwent primed constant infusion of [6,6-2H] glucose and muscle biopsies were taken before and following 90 min of cycling at 65% VO2max.
Results: E2 supplementation decreased the respiratory exchange ratio (RER, P = 0.03) and glucose Ra and Rd (both P = 0.04) during exercise, as compared with placebo (PL). E2 supplemenetation lowered proglycogen (P < 0.05) and total glycogen (P = 0.04) concentration, as compared with PL; however, there was no effect of E2 on net muscle glycogen utilization during exercise.
Conclusions: These findings show that E2 supplementation alters fuel selection in exercising men by increasing lipid use and reducing carbohydrate use, glucose Ra (primarily liver glucose production) and Rd (primarily muscle glucose uptake). Furthermore, E2 reduces the basal level of total muscle glycogen, particularly the proglycogen form.
-estradiol
muscle glycogen
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