In 2016, four studies were published that provided crucial new information on the endocrine actions of the hormone fibroblast growth factor 21 (FGF21). These studies provide a framework for the nutritional stimuli that regulate FGF21 expression and demonstrate a major role for FGF21 in primates and humans in regulating food intake, macronutrient preference and central reward pathways.
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References
Markan, K. R. & Potthoff, M. J. Metabolic fibroblast growth factors (FGFs): mediators of energy homeostasis. Semin. Cell Dev. Biol. 53, 85–93 (2016).
Talukdar, S. et al. A long-acting FGF21 molecule, PF-05231023, decreases body weight and improves lipid profile in non-human primates and type 2 diabetic subjects. Cell Metab. 23, 427–440 (2016).
Gaich, G. et al. The effects of LY2405319, an FGF21 analog, in obese human subjects with type 2 diabetes. Cell Metab. 18, 333–340 (2013).
von Holstein-Rathlou, S. et al. FGF21 mediates endocrine control of simple sugar intake and sweet taste preference by the liver. Cell Metab. 23, 335–343 (2016).
Chu, A. Y. et al. Novel locus including FGF21 is associated with dietary macronutrient intake. Hum. Mol. Genet. 22, 1895–1902 (2013).
Tanaka, T. et al. Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake. Am. J. Clin. Nutr. 97, 1395–1402 (2013).
Talukdar, S. et al. FGF21 regulates sweet and alcohol preference. Cell Metab. 23, 344–349 (2016).
Schumann, G. et al. KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference. Proc. Natl Acad. Sci. USA http://dx.doi.org/10.1073/pnas.1611243113 (2016).
Solon-Biet, S. M. et al. Defining the nutritional and metabolic context of FGF21 using the geometric framework. Cell Metab. 24, 555–565 (2016).
Laeger, T. et al. FGF21 is an endocrine signal of protein restriction. J. Clin. Invest. 124, 3913–3922 (2014).
Acknowledgements
The author's laboratory is supported by the NIH (grant R01DK106104) and the Fraternal Order of Eagles Diabetes Research Center.
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Potthoff, M. A new frontier in FGF21 biology. Nat Rev Endocrinol 13, 74–76 (2017). https://doi.org/10.1038/nrendo.2016.206
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DOI: https://doi.org/10.1038/nrendo.2016.206
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