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A pyrexic effect of FGF21 independent of energy expenditure and UCP1

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F21%3A00546860" target="_blank" >RIV/67985823:_____/21:00546860 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.molmet.2021.101324" target="_blank" >https://doi.org/10.1016/j.molmet.2021.101324</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.molmet.2021.101324" target="_blank" >10.1016/j.molmet.2021.101324</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A pyrexic effect of FGF21 independent of energy expenditure and UCP1

  • Original language description

    Objective: Administration of FGF21 to mice reduces body weight and increases body temperature. The increase in body temperature is generally interpreted as hyperthermia, i.e. a condition secondary to the increase in energy expenditure (heat production). Here, we examine an alternative hypothesis: that FGF21 has a direct pyrexic effect, i.e. FGF21 increases body temperature independently of any effect on energy expenditure. Methods: We studied the effects of FGF21 treatment on body temperature and energy expenditure in high-fat-diet-fed and chow-fed mice exposed acutely to various ambient temperatures, in high-fat diet-fed mice housed at 30 °C (i.e. at thermoneutrality), and in mice lacking uncoupling protein 1 (UCP1). Results: In every model studied, FGF21 increased body temperature, but energy expenditure was increased only in some models. The effect of FGF21 on body temperature was more (not less, as expected in hyperthermia) pronounced at lower ambient temperatures. Effects on body temperature and energy expenditure were temporally distinct (daytime versus nighttime). FGF21 enhanced UCP1 protein content in brown adipose tissue (BAT), there was no measurable UCP1 protein in inguinal brite/beige adipose tissue. FGF21 increased energy expenditure through adrenergic stimulation of BAT. In mice lacking UCP1, FGF21 did not increase energy expenditure but increased body temperature by reducing heat loss, e.g. a reduced tail surface temperature. Conclusion: The effect of FGF21 on body temperature is independent of UCP1 and can be achieved in the absence of any change in energy expenditure. Since elevated body temperature is a primary effect of FGF21 and can be achieved without increasing energy expenditure, only limited body weight-lowering effects of FGF21 may be expected.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30105 - Physiology (including cytology)

Result continuities

  • Project

    <a href="/en/project/GJ19-05356Y" target="_blank" >GJ19-05356Y: FGF21 effects on adipose tissue metabolism and their importance for treatment of metabolic syndrome</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Molecular Metabolism

  • ISSN

    2212-8778

  • e-ISSN

    2212-8778

  • Volume of the periodical

    53

  • Issue of the periodical within the volume

    Nov

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    16

  • Pages from-to

    101324

  • UT code for WoS article

    000702820300003

  • EID of the result in the Scopus database

    2-s2.0-85114918151