HMB attenuates muscle loss during sustained energy deficit induced by calorie restriction and endurance exercise
Abstract
Objective To investigate the efficacy and underlying mechanisms of β-hydroxy-β-methylbutyrate (HMB) on body composition, muscle mass and physical performance under catabolic versus normal training conditions.Materials/methods Mice were divided into four groups (n=10/group): (1) ALT=ad libitum+trained (1 h/d for 3 d/wk); (2) ALTH=ALT+HMB (0.5 g/kg BW/d); (3) C=calorie restricted (-30%)+trained (6 h/d, 6 d/wk); and (4) CH=C+HMB. Repeated in vivo assessments included body composition, grip strength and sensorimotor coordination before and after the experimental protocol, while in vitro analyses included muscle wet weights, expression of selected genes and proteins regulating muscle mass, and myofiber cross-sectional area. ANOVAs were used with significance set at p<0.05.Results ALTH had greater lean mass than ALT and sensorimotor function increased in ALTH, but decreased in ALT under normal training conditions. Grip strength decreased only in C, but was maintained in CH. Gastrocnemius mass and myofiber CSA were greater in CH than C following catabolic conditions. Gastrocnemius atrogin-1 mRNA expression was elevated in C but not in CH compared to all other groups whereas atrogin-1 protein levels showed no significant changes.Conclusion HMB improves body composition and sensorimotor function during normal training and attenuates muscle mass and strength loss during catabolic conditions.
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Preliminary data suggest that β-Hydroxy-β-methylbutyrate may attenuate lean mass loss during caloric restriction.
“Preliminary data suggest that β-Hydroxy-β-methylbutyrate may attenuate lean mass loss during caloric restriction [54].”
From Muscle loss and GLP-1R agonists use (2025) · cites this paper as [54]
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References 36 · Cited by 49
- Authors
- Park, B.-S., Henning, P. C., Grant, S. C., Lee, W. J., Lee, S.-R., Arjmandi, B. H., & Kim, J.-S.
- Affiliations
- Florida State University (US)
- Corresponding author
- Kim, Jeong-Su
- Venue
- Metabolism
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 62
- Issue
- 12
- Pages
- 1718-1729
- ISSN
- 0026-0495 (ISSN-L)
- OpenAlex
- W2116618309
- Cited by
- 49
- References
- 36
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 2 · 2023: 3 · 2022: 4 · 2021: 8 · 2020: 3 · 2019: 1 · 2018: 6 · 2017: 4 · 2016: 6 · 2015: 2 · 2014: 5 · 2013: 1
- FWCI
- 2.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
- Keywords
- beta-hydroxy-beta-methylbutyrate, muscle atrophy, caloric restriction, endurance exercise, negative energy balance, muscle mass, body composition, grip strength, sensorimotor coordination, atrogin-1, myofiber cross-sectional area, gastrocnemius, muscle catabolism
- MeSH terms
- Tripartite Motif Proteins, Animals, Body Composition, Diet, Energy Metabolism, Male, Mice, Inbred C57BL, Mitochondria, Muscle, Muscle Proteins, Neural Conduction, Organ Size, Physical Conditioning, Animal, Physical Endurance, Valerates, Blotting, Western, Muscle, Skeletal, Muscle Fibers, Skeletal, Hand Strength, Anatomy, Cross-Sectional, Caloric Restriction, Ubiquitin-Protein Ligases, SKP Cullin F-Box Protein Ligases, Mice, Muscle Strength, Real-Time Polymerase Chain Reaction
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