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Beta 2 -Adrenergic Stimulation Induces Resistance Training-Like Adaptations in Human Skeletal Muscle: Potential Role of KLHL41.

Authors :
Jessen S
Quesada JP
Di Credico A
Moreno-Justicia R
Wilson R
Jacobson G
Bangsbo J
Deshmukh AS
Hostrup M
Source :
Scandinavian journal of medicine & science in sports [Scand J Med Sci Sports] 2024 Oct; Vol. 34 (10), pp. e14736.
Publication Year :
2024

Abstract

Skeletal muscle mass plays a pivotal role in metabolic function, but conditions such as bed rest or injury often render resistance training impractical. The beta <subscript>2</subscript> -adrenergic receptor has been highlighted as a potential target to promote muscle hypertrophy and treat atrophic conditions. Here, we investigate the proteomic changes associated with beta <subscript>2</subscript> -adrenergic-mediated muscle hypertrophy, using resistance training as a hypertrophic comparator. We utilize MS-based proteomics to map skeletal muscle proteome remodeling in response to beta <subscript>2</subscript> -adrenergic stimulation or resistance training as well as cell model validation. We report that beta <subscript>2</subscript> -adrenergic stimulation mimics multiple features of resistance training in proteome-wide remodeling, comprising systematic upregulation of ribosomal subunits and concomitant downregulation of mitochondrial proteins. Approximately 20% of proteins were regulated in both conditions, comprising proteins involved in steroid metabolism (AKR1C1, AKR1C2, AKRC1C3), protein-folding (SERPINB1), and extracellular matrix organization (COL1A1, COL1A2). Among overall most significantly upregulated proteins were kelch-like family members (KLHL) 40 and 41. In follow-up experiments, we identify KLHL41 as having novel implications for beta <subscript>2</subscript> -adrenergic-mediated muscle hypertrophy. Treating C2C12 cells with beta <subscript>2</subscript> -agonist for 96 h increased myotube diameter by 48% (p < 0.001). This anabolic effect was abolished by prior knockdown of KLHL41. Using siRNA, KLHL41 abundance was decreased by 60%, and the anabolic response to beta <subscript>2</subscript> -agonist was diminished (+ 15%, i.e., greater in the presence of KLHL41, knock-down × treatment: p = 0.004). In conclusion, protein-wide remodeling induced by beta <subscript>2</subscript> -adrenergic stimulation mimics multiple features of resistance training, and thus the beta <subscript>2</subscript> -adrenergic receptor may be a target with therapeutic potential in the treatment of muscle wasting conditions without imposing mechanical load.<br /> (© 2024 The Author(s). Scandinavian Journal of Medicine & Science In Sports published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1600-0838
Volume :
34
Issue :
10
Database :
MEDLINE
Journal :
Scandinavian journal of medicine & science in sports
Publication Type :
Academic Journal
Accession number :
39366923
Full Text :
https://doi.org/10.1111/sms.14736