| Literature DB >> 26858428 |
João-Paulo G Camporez1, Max C Petersen2, Abulizi Abudukadier1, Gabriela V Moreira1, Michael J Jurczak3, Glenn Friedman4, Christopher M Haqq4, Kitt Falk Petersen1, Gerald I Shulman5.
Abstract
Sarcopenia, or skeletal muscle atrophy, is a debilitating comorbidity of many physiological and pathophysiological processes, including normal aging. There are no approved therapies for sarcopenia, but the antihypertrophic myokine myostatin is a potential therapeutic target. Here, we show that treatment of young and old mice with an anti-myostatin antibody (ATA 842) for 4 wk increased muscle mass and muscle strength in both groups. Furthermore, ATA 842 treatment also increased insulin-stimulated whole body glucose metabolism in old mice, which could be attributed to increased insulin-stimulated skeletal muscle glucose uptake as measured by a hyperinsulinemic-euglycemic clamp. Taken together, these studies provide support for pharmacological inhibition of myostatin as a potential therapeutic approach for age-related sarcopenia and metabolic disease.Entities:
Keywords: aging; insulin resistance; muscle mass; myostatin; sarcopenia
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Year: 2016 PMID: 26858428 PMCID: PMC4776508 DOI: 10.1073/pnas.1525795113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205