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The influence of Acute Beta-Hydroxy Beta-Methylbutyrate (HMB) ingestion on the human skeletal muscle transcriptome

The influence of Acute Beta-Hydroxy Beta-Methylbutyrate (HMB) ingestion on the human skeletal muscle transcriptome
The influence of Acute Beta-Hydroxy Beta-Methylbutyrate (HMB) ingestion on the human skeletal muscle transcriptome

Background: nutritional interventions to mitigate age/disease-related skeletal muscle attrition are much needed given the growing older population. Beta-hydroxy beta-methylbutyrate (HMB), an endogenous metabolite of the essential amino acid leucine, has anabolic properties in skeletal muscle: acutely stimulating muscle protein synthesis and attenuating muscle protein breakdown. While the role of supplemental HMB on muscle protein turnover is established, mechanistic effects on the muscle transcriptome have not been examined. 

Methods: total RNA was extracted from m. vastus lateralis muscle biopsies of young males ( n = 14) before and ~2.5 h after oral consumption of ~3 g HMB. Global changes in the muscle transcriptome were assessed via RNA sequencing, and differential expression in genes between fasted and 'fed' (HMB) conditions was determined. To identify the functional biology of differentially expressed genes, gene set enrichment and active subnetwork-orientated enrichment analyses was performed. 

 Results: of 15,982 genes detected, 468 were significantly upregulated and 326 were significantly downregulated in response to HMB. These genes were found to be associated with molecular pathways regulating muscle protein turnover, most notably, JAK-STAT signalling (e.g., STAM), circadian rhythm (e.g., NR1D1, NR1D2, PER2, PER3), TNFα signalling (e.g., TNFRSF1A, CCL2, CXCL2), and protein synthesis (e.g., POLR1A, POLR2A, POLR3A, PIK3RR, SGK1). HMB also regulated the expression of AA transporters, evoking a robust increase in SLC36A1 ( PAT1) and SLC7A5 ( LAT1). 

 Conclusions: HMB evokes transcriptional events important in the homeostasis of muscle, supporting a role in proteostasis and one akin to protein intake, i.e., upregulation of AA transporters. Future work should further define HMB's transcriptomic/proteomic effects in ageing/disease and synergy with exercise.

Adult, Humans, Male, Muscle Proteins/metabolism, Muscle, Skeletal/metabolism, Transcriptome/drug effects, Valerates/administration & dosage, Young Adult, RNA sequencing, transcriptome, inflammation, circadian rhythm, beta-hydroxy beta-methylbutyrate (HMB), skeletal muscle, amino acid transporters
2072-6643
Wilkinson, Daniel J.
72380ed8-6660-40ce-acec-2d65ef3045c4
Gallagher, Iain J.
dc144e9d-d0da-473f-b0c4-371a60246321
Crossland, Hannah
243567e1-09e8-43f5-bdac-6ee9ed5e5f22
Pereira, Suzette L.
672916f5-2b99-4b0d-8c17-f1f8b0ee91cf
Rueda, Ricardo
a9c1592b-1a2d-4e9a-b56d-5a34774117c7
Phillips, Bethan E.
9461226a-1d19-4953-bdb3-41fc560a21f4
Smith, Kenneth
4bc77c16-88fb-450c-8c11-a1485339c08d
Deane, Colleen S.
3320532e-f411-4ea8-9a14-4a9f248da898
Atherton, Philip J.
b9c1604a-deaa-4174-8b72-e564dd72dd68
Wilkinson, Daniel J.
72380ed8-6660-40ce-acec-2d65ef3045c4
Gallagher, Iain J.
dc144e9d-d0da-473f-b0c4-371a60246321
Crossland, Hannah
243567e1-09e8-43f5-bdac-6ee9ed5e5f22
Pereira, Suzette L.
672916f5-2b99-4b0d-8c17-f1f8b0ee91cf
Rueda, Ricardo
a9c1592b-1a2d-4e9a-b56d-5a34774117c7
Phillips, Bethan E.
9461226a-1d19-4953-bdb3-41fc560a21f4
Smith, Kenneth
4bc77c16-88fb-450c-8c11-a1485339c08d
Deane, Colleen S.
3320532e-f411-4ea8-9a14-4a9f248da898
Atherton, Philip J.
b9c1604a-deaa-4174-8b72-e564dd72dd68

Wilkinson, Daniel J., Gallagher, Iain J., Crossland, Hannah, Pereira, Suzette L., Rueda, Ricardo, Phillips, Bethan E., Smith, Kenneth, Deane, Colleen S. and Atherton, Philip J. (2026) The influence of Acute Beta-Hydroxy Beta-Methylbutyrate (HMB) ingestion on the human skeletal muscle transcriptome. Nutrients, 18 (3), [434]. (doi:10.3390/nu18030434).

Record type: Article

Abstract

Background: nutritional interventions to mitigate age/disease-related skeletal muscle attrition are much needed given the growing older population. Beta-hydroxy beta-methylbutyrate (HMB), an endogenous metabolite of the essential amino acid leucine, has anabolic properties in skeletal muscle: acutely stimulating muscle protein synthesis and attenuating muscle protein breakdown. While the role of supplemental HMB on muscle protein turnover is established, mechanistic effects on the muscle transcriptome have not been examined. 

Methods: total RNA was extracted from m. vastus lateralis muscle biopsies of young males ( n = 14) before and ~2.5 h after oral consumption of ~3 g HMB. Global changes in the muscle transcriptome were assessed via RNA sequencing, and differential expression in genes between fasted and 'fed' (HMB) conditions was determined. To identify the functional biology of differentially expressed genes, gene set enrichment and active subnetwork-orientated enrichment analyses was performed. 

 Results: of 15,982 genes detected, 468 were significantly upregulated and 326 were significantly downregulated in response to HMB. These genes were found to be associated with molecular pathways regulating muscle protein turnover, most notably, JAK-STAT signalling (e.g., STAM), circadian rhythm (e.g., NR1D1, NR1D2, PER2, PER3), TNFα signalling (e.g., TNFRSF1A, CCL2, CXCL2), and protein synthesis (e.g., POLR1A, POLR2A, POLR3A, PIK3RR, SGK1). HMB also regulated the expression of AA transporters, evoking a robust increase in SLC36A1 ( PAT1) and SLC7A5 ( LAT1). 

 Conclusions: HMB evokes transcriptional events important in the homeostasis of muscle, supporting a role in proteostasis and one akin to protein intake, i.e., upregulation of AA transporters. Future work should further define HMB's transcriptomic/proteomic effects in ageing/disease and synergy with exercise.

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Accepted/In Press date: 23 January 2026
e-pub ahead of print date: 28 January 2026
Published date: 28 January 2026
Keywords: Adult, Humans, Male, Muscle Proteins/metabolism, Muscle, Skeletal/metabolism, Transcriptome/drug effects, Valerates/administration & dosage, Young Adult, RNA sequencing, transcriptome, inflammation, circadian rhythm, beta-hydroxy beta-methylbutyrate (HMB), skeletal muscle, amino acid transporters

Identifiers

Local EPrints ID: 510132
URI: http://eprints.soton.ac.uk/id/eprint/510132
ISSN: 2072-6643
PURE UUID: 583adba0-2da8-4c01-9fbd-8241edf6da3c
ORCID for Colleen S. Deane: ORCID iD orcid.org/0000-0002-2281-6479

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Date deposited: 18 Mar 2026 17:32
Last modified: 19 Mar 2026 03:06

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Contributors

Author: Daniel J. Wilkinson
Author: Iain J. Gallagher
Author: Hannah Crossland
Author: Suzette L. Pereira
Author: Ricardo Rueda
Author: Bethan E. Phillips
Author: Kenneth Smith
Author: Colleen S. Deane ORCID iD
Author: Philip J. Atherton

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