Cited by 49Muscle metabolism and nutritionMuscle Physiology and DisordersNutrition and Health in Aging

HMB attenuates muscle loss during sustained energy deficit induced by calorie restriction and endurance exercise

Park, Bong-Sup, Henning, Paul C., Grant, Samuel C., Lee, Won Jun, Lee, Sang-Rok, Arjmandi, Bahram H., Kim, Jeong-Su·2013·Metabolism

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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Crossref · 10.1016/j.metabol.2013.06.005

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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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