Atomoxetine Prevents Dexamethasone-Induced Skeletal Muscle Atrophy in Mice

作者：Jesinkey Sean R; Korrapati Midhun C; Ra**ach Kyle A; Beeson Craig C; Schnellmann Rick G^*

来源：Journal of Pharmacology and Experimental Therapeutics, 2014, 351(3): 663-673.

DOI：10.1124/jpet.114.217380

Skeletal muscle atrophy remains a clinical problem in numerous pathologic conditions. beta(2)-Adrenergic receptor agonists, such as formoterol, can induce mitochondrial biogenesis (MB) to prevent such atrophy. Additionally, atomoxetine, an FDA-approved norepinephrine reuptake inhibitor, was positive in a cellular assay for MB. We used a mouse model of dexamethasone-induced skeletal muscle atrophy to investigate the potential role of atomoxetine and formoterol to prevent muscle mass loss. Mice were administered dexamethasone once daily in the presence or absence of formoterol (0.3 mg/kg), atomoxetine (0.1 mg/kg), or sterile saline. Animals were euthanized at 8, 16, and 24 hours or 8 days later. Gastrocnemius muscle weights, changes in mRNA and protein expression of peroxisome proliferator-activated receptor-gamma coactivator-1 alpha (PGC-1 alpha) isoforms, ATP synthase beta, cytochrome c oxidase subunit I, NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, ND1, insulin-like growth factor 1 (IGF-1), myostatin, muscle Ring-finger protein-1 (muscle atrophy), phosphorylated forkhead box protein O 3a (p-FoxO3a), Akt, mammalian target of rapamycin (mTOR), and ribosomal protein S6 (rp-S6; muscle hypertrophy) in naive and muscle-atrophied mice were measured. Atomoxetine increased p-mTOR 24 hours after treatment in naive mice, but did not change any other biomarkers. Formoterol robustly activated the PGC-1 alpha-4-IGF1-Akt-mTOR-rp-S6 pathway and increased p-FoxO3a as early as 8 hours and repressed myostatin at 16 hours. In contrast to what was observed with acute treatment, chronic treatment (7 days) with atomoxetine increased p-Akt and p-FoxO3a, and sustained PGC-1 alpha expression and skeletal muscle mass in dexamethasone-treated mice, in a manner comparable to formoterol. In conclusion, chronic treatment with a low dose of atomoxetine prevented dexamethasone-induced skeletal muscle wasting and supports a potential role in preventing muscle atrophy.

• 出版日期2014-12