Ontology highlight
ABSTRACT: Background
Systemic administration of beta-adrenoceptor (beta-AR) agonists has been found to induce skeletal muscle hypertrophy and significant metabolic changes. In the context of energy homeostasis, the importance of beta-AR signaling has been highlighted by the inability of beta(1-3)-AR-deficient mice to regulate energy expenditure and susceptibility to diet induced obesity. However, the molecular pathways and gene expression changes that initiate and maintain these phenotypic modulations are poorly understood. Therefore, the aim of this study was to identify differential changes in gene expression in murine skeletal muscle associated with systemic (acute and chronic) administration of the beta(2)-AR agonist formoterol.Results
Skeletal muscle gene expression (from murine
SUBMITTER: Pearen MA
PROVIDER: S-EPMC2758907 | biostudies-literature | 2009 Sep
REPOSITORIES: biostudies-literature