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pmid:34909668
Chronic treatment with terbutaline increases glucose and oleic acid oxidation and protein synthesis in cultured human myotubes.
Christine Skagen · Tuula A Nyman · Xiao-Rong Peng · Gavin O'Mahony · Eili Tranheim Kase · Arild Chr Rustan · G Hege Thoresen
Current research in pharmacology and drug discovery · 2021 doi:10.1016/j.crphar.2021.100039
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Complete file
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Although these effects have been widely studied in vivo, the in vitro data are limited to mouse and rat cell lines. Therefore, we sought to discover the effects of the β2-adrenergic receptor agonist terbutaline on metabolism and protein synthesis in human primary skeletal muscle cells.\nMETHODS: Human cultured myotubes were exposed to terbutaline in various concentrations (0.01-30 μM) for 4 or 96 h. Thereafter uptake of [14C]deoxy-D-glucose, oxydation of [14C]glucose and [14C]oleic acid were measured. Incorporation of [14C]leucine, gene expression by qPCR and proteomics analyses by mass spectrometry by the STAGE-TIP method were performed after 96 h exposure to 1 and 10 μM of terbutaline.\nRESULTS: The results showed that 4 h treatment with terbutaline in concentrations up to 1 μM increased glucose uptake in human myotubes, but also decreased both glucose and oleic acid oxidation along with oleic acid uptake in concentrations of 10-30 μM. Moreover, administration of terbutaline for 96 h increased glucose uptake (in terbutaline concentrations up to 1 μM) and oxidation (1 μM), as well as oleic acid oxidation (0.1-30 μM), leucine incorporation into cellular protein (1-10 μM) and upregulated several pathways related to mitochondrial metabolism (1 μM). 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