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Lonafarnib Protects Against Muscle Atrophy Induced by Dexamethasone
Sanghoon Bae1, Van-Hieu Mai2, Seyoung Mun3,4,5,6
1Department of Nanobiomedical Science & BK21 NBM Global Research Center for Regenerative Medicine, Dankook University, Cheonan, Korea.
Background:
Muscle atrophy, including glucocorticoid-induced muscle wasting from treatments such as dexamethasone (DEX), results in significant reductions in muscle mass, strength and function. This study investigates the potential of lonafarnib, a farnesyltransferase inhibitor, to counteract DEX-induced muscle atrophy by targeting key signalling pathways.
Methods:
We utilized in vitro models with C2C12 myotubes treated with DEX and in vivo models with Caenorhabditis elegans and DEX-treated Sprague-Dawley rats. Myotube morphology was assessed by measuring area, fusion index and diameter. Muscle function was evaluated by grip strength and compound muscle action potential (CMAP) in the gastrocnemius (GC) and tibialis anterior (TA) muscles. Molecular mechanisms were explored through RNA sequencing and Western blotting to assess changes in mitochondrial function and muscle signalling pathways.
Results:
Lonafarnib (2 μM) significantly improved myotube area (1.49 ± 0.14 × 105 μm2 vs. 1.03 ± 0.49 × 105 μm2 in DEX, p < 0.05), fusion index (18.73 ± 1.23% vs. 13.3 ± 1.56% in DEX, p < 0.05) and myotube diameter (31.89 ± 0.89 μm vs. 21.56 ± 1.01 μm in DEX, p < 0.05) in C2C12 myotubes. In C. elegans, lonafarnib (100 μM) increased the pharyngeal pumping rate from 212 ± 7.21 contractions/min in controls to 308 ± 17.09 contractions/min at day 4 (p < 0.05), indicating enhanced neuromuscular function. In DEX-induced atrophic rats, lonafarnib improved maximal grip strength (DEX: 13.91 ± 0.78 N vs. 1 μM lonafarnib: 16.18 ± 0.84 N and 5 μM lonafarnib: 16.71 ± 0.83 N, p < 0.05), increased muscle weight in GC, and enhanced CMAP amplitudes in both GC and TA muscles. Western blot analysis showed that lonafarnib treatment upregulated UCP3 and ANGPTL4 and increased phosphorylation of mTOR and S6 ribosomal protein (p < 0.05), indicating enhanced mitochondrial function and protein synthesis. Knockdown models further demonstrated that lonafarnib could partially rescue muscle atrophy phenotypes, indicating its action through multiple molecular pathways.
Conclusions:
Lonafarnib mitigates dexamethasone-induced muscle atrophy by enhancing mitochondrial function and activating anabolic pathways. These findings support further investigation of lonafarnib as a therapeutic agent for muscle atrophy in clinical settings.
Insights
Lonafarnib, a farnesyltransferase inhibitor, effectively combats muscle atrophy induced by dexamethasone (DEX). This drug enhances mitochondrial function and anabolic pathways, showing promise as a therapeutic for muscle wasting conditions.
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Glucocorticoids like dexamethasone (DEX) cause muscle atrophy, leading to reduced muscle mass, strength, and function.
- Muscle wasting significantly impacts patient mobility and quality of life, necessitating effective therapeutic interventions.
Purpose of the Study:
- To investigate the efficacy of lonafarnib, a farnesyltransferase inhibitor, in counteracting dexamethasone-induced muscle atrophy.
- To elucidate the molecular mechanisms underlying lonafarnib's effects on muscle signaling pathways and mitochondrial function.
Main Methods:
- Utilized in vitro (C2C12 myotubes) and in vivo (C. elegans, Sprague-Dawley rats) models of dexamethasone-induced muscle atrophy.
- Assessed myotube morphology, muscle function (grip strength, CMAP), and molecular changes via RNA sequencing and Western blotting.
Main Results:
- Lonafarnib significantly improved myotube size, fusion index, and diameter in vitro.
- In vivo studies showed lonafarnib enhanced neuromuscular function in C. elegans and improved grip strength, muscle weight, and CMAP in rats.
- Molecular analysis revealed lonafarnib upregulated UCP3 and ANGPTL4, and increased mTOR/S6 phosphorylation, indicating enhanced mitochondrial function and protein synthesis.
Conclusions:
- Lonafarnib effectively mitigates dexamethasone-induced muscle atrophy.
- The drug's mechanism involves enhancing mitochondrial function and activating anabolic pathways.
- Lonafarnib warrants further investigation as a potential therapeutic agent for clinical muscle atrophy treatment.
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