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McGill Nutrition and Food Science Centre and
*
Division of Geriatric Medicine, Royal Victoria Hospital, Montreal, Canada;
School of Health and Physical Education, Queens University, Kingston, Ontario, Canada;
Research Institute, Hospital for Sick Children, Departments of Paediatrics and Nutritional Sciences, University of Toronto, Toronto, Ontario, Canada; and
§
School of Dietetics and Human Nutrition, Mac Donald Campus, McGill University, Montreal, Canada
2To whom correspondence should be addressed.
We tested the hypothesis that nonmuscle lean tissue mass and its rate
of protein catabolism remain constant with aging despite changes in the
proportional contribution of these tissues to whole-body protein
metabolism. Whole-body protein kinetics, using the 60-h oral
[15 N]glycine method, and muscle and nonmuscle protein
catabolism, based on protein kinetic data, urinary
N
-methylhistine excretion and lean tissue volumes
defined by whole-body magnetic resonance imaging, from eight
healthy elderly subjects (5 females and 3 males, mean age 71.5 y)
were compared with those of seven young persons (3 females and 4 males,
mean age 28 y). There were no significant age or gender effects on
rates of protein kinetics per L total lean tissue. There was a lower
(P < 0.004) rate of muscle protein catabolism in
the elderly (1.8 ± 0.2 vs. 2.6 ± 0.1 g ·
L-1 · d-1) and a trend
(P = 0.08) for lower muscle volume (19.7 ± 1.5 vs. 25.0 ± 2.4 L). This contrasted with intraabdominal lean
tissue, where the rate of protein catabolism (13.8 ± 0.6 vs. 13.2
± 0.9 g · L-1 · d-1) and
volume (7.5 ± 0.3 vs 8.0 ± 0.5 L) did not differ between
age groups. Thus, the decrease in the contribution by muscle to
whole-body protein metabolism with age is associated with an
increase from 62 to 74% (P < 0.001) in the
contribution by nonmuscle lean tissues. These findings have potential
implications for the nutrition of both normal and sick elderly
persons.
KEY WORDS: protein turnover aging N
-methylhistidine magnetic resonance imaging elderly humans
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