Physical activity and eating are two major physiological muscle growth stimuli. Although muscle protein turnover rates are not different in young and middle-aged men and women, we recently found that the basal rate of muscle protein synthesis is greater and the anabolic response to mixed-meal intake is blunted in 65- to 80-yr-old women compared with men of the same age. Whether older women are also resistant to the anabolic effect of exercise is not known.
We measured the rate of muscle protein synthesis (both during basal, postabsorptive conditions and during mixed-meal intake) before and after 3 months of exercise training in obese, 65- to 80-yr-old men and women.
At the beginning of the study (before training) the basal, postabsorptive muscle protein fractional synthesis rate (FSR) was significantly greater in women than in men (0.064 ± 0.006%·h−1 vs 0.039 ± 0.006%·h−1, respectively, P < 0.01), whereas the meal-induced increase in the muscle protein FSR was greater in men than in women (P < 0.05). In men, exercise training approximately doubled the basal muscle protein FSR (P = 0.001) but had no effect on the meal-induced increase in muscle protein FSR (P = 0.78). In women, exercise training increased the muscle protein FSR by ∼40% (P = 0.03) and also had no effect on the meal-induced increase in muscle protein FSR (P = 0.51).
These results suggest that there is significant sexual dimorphism not only in the basal, postabsorptive rate of muscle protein synthesis but also in the anabolic response to feeding and exercise training in obese, older adults.
1Center for Human Nutrition, Division of Geriatrics and Nutritional Science, Washington University School of Medicine, St. Louis, MO; and 2Program in Physical Therapy, Washington University School of Medicine, St. Louis, MO
Address for correspondence: Bettina Mittendorfer, Ph.D., Center for Human Nutrition, Washington University School of Medicine, 660 S. Euclid Ave., Campus Box 8031, St. Louis, MO 63110; E-mail: firstname.lastname@example.org.
Submitted for publication August 2011.
Accepted for publication December 2011.