Fibroblast growth factor-21 is induced in human skeletal muscles by hyperinsulinemia
- Pernille Hojman (Pernille.Hoejman.Moeller{at}rh.regionh.dk),
- Maria Pedersen,
- Anders Rinnov Nielsen,
- Rikke Krogh-Madsen,
- Christina Yfanti,
- Thorbjørn Åkerstrom,
- Søren Nielsen and
- Bente Klarlund Pedersen
- Centre of Inflammation and Metabolism at Department of Infectious Diseases, Rigshospitalet, University of Copenhagen, Denmark
Abstract
Objective: Fibroblast growth factor–21 (FGF-21) is a potent metabolic regulator, which in animal models has been shown to improve glucose metabolism and insulin sensitivity. Recently, FGF-21 was shown to be expressed and secreted from murine muscle cells in response to insulin stimulation.
Research design and Methods: We studied muscular FGF-21 expression and plasma FGF-21 after acute insulin stimulation in young healthy men during a hyperinsulinemic euglycemic clamp. Furthermore, we investigated systemic levels and muscle FGF-21 expression in humans with or without insulin resistance and chronic elevated insulin.
Results: FGF-21 was barely detectable in young healthy males before insulin infusion. After 3 or-4 hours of insulin infusion during a hyperinsulinemic euglycemic clamp muscular FGF-21 expression increased significantly. Plasma FGF-21 followed the same pattern. In individuals with chronic elevated insulin, muscular FGF-21 expression was associated with hyperinsulinemia in men, but not in women. In plasma, hyperinsulinemia as well as fasting glucose was positively associated with plasma FGF-21, while plasma FGF-21 correlated negatively with HDL-cholesterol. No associations between muscle and plasma FGF-21 were found in the individuals with chronic hyperinsulinemia.
Conclusions: In conclusion, FGF-21 is expressed in human skeletal muscle in response to insulin stimulation, suggesting that FGF-21 is an insulin-regulated myokine. In support, we found an association between chronic hyperinsulinemia and levels of FGF-21.
Footnotes
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- Received May 13, 2009.
- Accepted August 9, 2009.
- Copyright © American Diabetes Association











