Resistance training preserves fat-free mass without impacting changes in protein metabolism after weight loss in older women - PubMed (original) (raw)
Randomized Controlled Trial
doi: 10.1038/oby.2009.2. Epub 2009 Feb 26.
Affiliations
- PMID: 19247271
- PMCID: PMC4299870
- DOI: 10.1038/oby.2009.2
Randomized Controlled Trial
Resistance training preserves fat-free mass without impacting changes in protein metabolism after weight loss in older women
Wayne W Campbell et al. Obesity (Silver Spring). 2009 Jul.
Abstract
This study assessed the effects of resistance training (RT) on energy restriction-induced changes in body composition, protein metabolism, and the fractional synthesis rate of mixed muscle proteins (FSRm) in postmenopausal, overweight women. Sixteen women (age 68 +/- 1 years, BMI 29 +/- 1 kg/m(2), mean +/- s.e.m.) completed a 16-week controlled diet study. Each woman consumed 1.0 g protein/kg/day. At baseline (weeks B1-B3) and poststudy (weeks RT12-RT13), energy intake matched each subject's need and during weeks RT1-RT11 was hypoenergetic by 2,092 kJ/day (500 kcal/day). From weeks RT1 to RT13, eight women performed RT 3 day/week (RT group) and eight women remained sedentary (SED group). RT did not influence the energy restriction-induced decrease in body mass (SED -5.8 +/- 0.6 kg; RT -5.0 +/- 0.2 kg) and fat mass (SED -4.1 +/- 0.9 kg; RT -4.7 +/- 0.5 kg). Fat free mass (FFM) and total body water decreased in SED (-1.6 +/- 0.4 and -2.1 +/- 0.5 kg) and were unchanged in RT (-0.3 +/- 0.4 and -0.4 +/- 0.7 kg) (group-by-time, P < or = 0.05 and P = 0.07, respectively). Protein-mineral mass did not change in either group (SED 0.4 +/- 0.2 kg; RT 0.1 +/- 0.4 kg). Nitrogen balance, positive at baseline (2.2 +/- 0.3 g N/day), was unchanged poststudy. After body mass loss, postabsorptive (PA) and postprandial (PP) leucine turnover, synthesis, and breakdown decreased. Leucine oxidation and balance were not changed. PA and total (PA + PP) FSRm in the vastus lateralis were higher after weight loss. RT did not influence these protein metabolism responses. In summary, RT helps older women preserve FFM during body mass loss. The comparable whole-body nitrogen retentions, leucine kinetics, and FSRm between groups are consistent with the lack of differential protein-mineral mass change.
Conflict of interest statement
DISCLOSURE
The authors declared no conflict of interest.
Figures
Figure 1
Experimental design and approximate study schedule of the 16-week protocol that included a 3-week baseline period (B1–B3) and an 11-week period of intervention (dietary energy restriction with (n = 8) or without (n = 8) resistance training (RT1–RT11), and a 2-week postintervention period (RT12–RT13)).
Figure 2
Protocol for L-[1-13C]leucine and L-[_ring_-2H5]phenylalanine infusion used to measure whole-body protein turnover and mixed muscle fractional synthesis rate, respectively. X indicates the time that a beverage was provided, resting energy expenditure (REE) measurement completed, blood draw and breath samples were taken, and muscle biopsy procedure performed. ↓ indicates the administration of the priming doses of NaH13CO3, L-[1-13C]leucine and L-[_ring_-2H5]phenylalanine. Beverages contained 8.33% of each subject’s estimated daily energy and dietary protein needs.
Figure 3
Body mass and composition changes after an 11-week period of energy restriction in overweight postmenopausal women who were sedentary (n = 8) or resistance training (n = 8). FFM, fat-free mass; PMM, protein–mineral mass; TBW, total body water. Differential response between the sedentary and resistance training groups, group-by-time interaction, *P ≤ 0.05; †P = 0.07.
Figure 4
Changes in the rates of whole-body leucine turnover (Flux), synthesis (Syn), and oxidation (Ox) after an 11-week period of energy restriction–induced body mass loss in overweight postmenopausal women who were sedentary (n = 8) or who were resistance training (n = 8). The rates were measured during an 8-h primed, constant infusion of L-[1-13C]leucine while the subjects were in postabsorptive and postprandial states, and the changes calculated as postintervention − baseline. Values are mean ± s.e.m. *Significant main effect of time, P ≤ 0.05.
Figure 5
Fractional synthesis rate of mixed muscle proteins (FSRm) in the vastus lateralis before (baseline) and after (resistance training week 12, RT12) an 11-week period of energy restriction–induced body mass loss in overweight postmenopausal women who were sedentary (n = 8) or resistance training (n = 8). The FSRm was measured during an 8-h primed, constant infusion of L-[_ring_-2H5]phenylalanine while the subjects were in postabsorptive and postprandial states. Total FSRm was measured from the incorporation of isotope during the postabsorptive and postprandial periods combined. Values are mean ± s.e.m. *Significant main effect of metabolic state (postabsorptive vs. postprandial) at baseline, P ≤ 0.05. †Significant main effect of time (baseline vs. week R12), P ≤ 0.05.
References
- Baumgartner RN. Body composition in healthy aging. Ann NY Acad Sci. 2000;904:437–448. - PubMed
- Villareal DT, Apovian CM, Kushner RF, Klein S. Obesity in older adults: technical review and position statement of the American Society for Nutrition and NAASO, The Obesity Society. Obes Res. 2005;13:1849–1863. - PubMed
- Jakicic JM, Clark K, Coleman E, et al. American College of Sports Medicine position stand. Appropriate intervention strategies for weight loss and prevention of weight regain for adults. Med Sci Sports Exerc. 2001;33:2145–2156. - PubMed
- Gallagher D, Kovera AJ, Clay-Williams G, et al. Weight loss in postmenopausal obesity: no adverse alterations in body composition and protein metabolism. Am J Physiol Endocrinol Metab. 2000;279:E124–E131. - PubMed
- Miller SL, Wolfe RR. The danger of weight loss in the elderly. J Nutr Health Aging. 2008;12:487–491. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- MO1 RR14288/RR/NCRR NIH HHS/United States
- 1 R29 AG13409/AG/NIA NIH HHS/United States
- 1 R01 AG15750/AG/NIA NIH HHS/United States
- R01 AG015750/AG/NIA NIH HHS/United States
- M01 RR014288/RR/NCRR NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous