FGF21 regulates sweet and alcohol preference

Saswata Talukdar, Bryn M. Owen, Parkyong Song, Genaro Hernandez, Yuan Zhang, Yingjiang Zhou, William T. Scott, Bhavna Paratala, Tod Turner, Andrew Smith, Barbara Bernardo, Christian P. Müller, Hao Tang, David J. Mangelsdorf*, Bryan Goodwin, Steven A. Kliewer

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    241 Citations (Scopus)

    Abstract

    Fibroblast growth factor 21 (FGF21) is a hormone induced by various metabolic stresses, including ketogenic and high-carbohydrate diets, that regulates energy homeostasis. In humans, SNPs in and around the FGF21 gene have been associated with macronutrient preference, including carbohydrate, fat, and protein intake. Here we show that FGF21 administration markedly reduces sweet and alcohol preference in mice and sweet preference in cynomolgus monkeys. In mice, these effects require the FGF21 co-receptor β-Klotho in the central nervous system and correlate with reductions in dopamine concentrations in the nucleus accumbens. Since analogs of FGF21 are currently undergoing clinical evaluation for the treatment of obesity and type 2 diabetes, our findings raise the possibility that FGF21 administration could affect nutrient preference and other reward behaviors in humans.

    Original languageEnglish
    Pages (from-to)344-349
    Number of pages6
    JournalCELL METABOLISM
    Volume23
    Issue number2
    Early online date24 Dec 2015
    DOIs
    Publication statusPublished - 9 Feb 2016

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