期刊
GROWTH HORMONE & IGF RESEARCH
卷 26, 期 -, 页码 36-41出版社
CHURCHILL LIVINGSTONE
DOI: 10.1016/j.ghir.2015.12.008
关键词
lrisin; FNDC5; Growth hormone; IGF-I; Skeletal muscle; Mitochondrial; Obesity
资金
- NIH [K23DK087857, 1UL1RR025758-04, 8UL1TR000170-05, M01RR01066, UL1 TR001102]
- National Center for Research Resources
- National Center for Advancing Translational Sciences
Objective: To investigate the relationship of skeletal muscle FNDC5 mRNA expression and circulating irisin to the GH/IGF-I axis and to skeletal muscle mitochondrial function and mitochondria-related gene expression in obese men. Design: Fifteen abdominally obese men with reduced growth hormone received 12 weeks of recombinant human GH (rhGH). Before and after treatment, they underwent P-31-magnetic resonance spectroscopy to evaluate phosphocreatine (PCr) recovery as a measure of mitochondrial function and skeletal muscle biopsy to assess expression of mitochondrial-related genes. Serum irisin and IGF-I and skeletal muscle FNDC5 and IGF-I mRNA were measured. Results: At baseline, skeletal muscle FNDC5 mRNA was significantly and positively associated with IGF-I mRNA (rho = 0.81, P = 0.005) and rate of PCr recovery (rho = 0.79, P = 0.006). Similar relationships of circulating irisin to IGF-I mRNA (rho = 0.63, P = 0.05) and rate of PCr recovery (rho = 0.48, P = 0.08) were demonstrated, but were not as robust as those with muscle FNDC5 expression. Both serum irisin and skeletal muscle FNDC5 mRNA were significantly associated with PPAR gamma (rho = 0.73, P = 0.02 and rho = 0.85, P = 0.002), respectively. In addition, FNDC5 mRNA was correlated with skeletal muscle PGC-1 alpha (rho = 0.68, P = 0.03), NRF1 (rho = 0.66, P = 0.04) and TFAM (rho = 0.79, P = 0.007) mRNA. Neither serum irisin nor muscle mRNA expression of FNDC5 changed with rhGH treatment. Conclusion: These novel data in skeletal muscle demonstrate that local expression of FNDC5 is associated with mRNA expression of IGF-I and mitochondrial function and mitochondria-related gene expression in obese subjects with reduced growth hormone and suggest a potential role for FNDC5 acting locally in muscle in a low GH state. Further studies are needed to clarify the relationship between the GH/IGF-I axis and irisin. (C) 2015 Elsevier Ltd. All rights reserved.
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