Long-term caloric restriction abrogates the age-related decline in skeletal muscle aerobic function
Abstract
The purpose of this study was to determine the effect of long-term caloric restriction (CR) on the age-associated decline of skeletal muscle aerobic function. Skeletal muscle maximal aerobic performance (VO2max) was assessed in ad libitum (AL) and CR rats aged 8-10 months and 35 months using a pump-perfused hindlimb model to match oxygen delivery to muscle mass between groups. Whereas there was a 46% decline in muscle mass-specific VO2max between 8-10 mo (524+/-13 micromol x min(-1) x 100 g(-1); mean+/- SE) and 35 mo (281+/-54 micromol x min(-1) x 100 g(-1)) in AL rats, not only did CR rats begin at the same point in 8-10 mo old rats (490+/-42 micromol x min(-1) x 100 g(-1)), we found no decline in 35 mo old CR animals (484+/-49 micromol x min(-1) x 100 g(-1)). Interestingly, although most markers of oxidative capacity began at a lower point in young adult CR animals, CR rats exhibited a higher in situ activity of complex IV at VO2max. This activity allows the young adult CR animals to exhibit normal aerobic capacity despite the lower oxidative enzyme activities. In stark contrast to the 19-41% decline in activities of citrate synthase, complexes I-III, and complex IV in homogenates prepared from the plantaris muscle and mixed region of gastrocnemius muscle with aging in AL rats, no age-related decline was found in CR animals. Thus, our results showed that CR preserves aerobic function in aged skeletal muscles by facilitating a higher in situ function of complex IV and by preventing the age-related decline in mitochondrial oxidative capacity.
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In rodents, 40% caloric restriction prevents the age-associated decline in muscle mitochondrial function and aerobic capacity.
“In rodents, 40% CR prevents the age-associated decline in muscle mitochondrial function 149, 150 and aerobic capacity.150”
From Hormonal and Metabolic Changes of Aging and the Influence of Lifestyle Modifications (2021) · cites this paper as [150]
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References 53 · Cited by 80
- Authors
- Hepple, R. T., Baker, D. J., Kaczor, J. J., & Krause, D. J.
- Affiliations
- University of Calgary (CA)
- McMaster University (CA)
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 2005-06-14
- Volume
- 19
- Issue
- 10
- Pages
- 1320-1322
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W2055729903
- Cited by
- 80
- References
- 53
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 1 · 2022: 4 · 2021: 3 · 2020: 2 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 4 · 2015: 7 · 2014: 3 · 2013: 4 · 2012: 6
- FWCI
- 1.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The FASEB Journal (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research (MOP 57808)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- caloric restriction, skeletal muscle aging, cardiorespiratory fitness, VO2max, mitochondrial complex IV, oxidative capacity, citrate synthase, mitochondrial respiration, age-related decline, hindlimb perfusion, plantaris muscle, gastrocnemius
- MeSH terms
- Aerobiosis, Aging, Animals, Electron Transport Complex IV, Mitochondria, Motor Activity, Muscle Contraction, Oxidation-Reduction, Oxygen Consumption, Rats, Inbred F344, Muscle, Skeletal, Caloric Restriction, Rats
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