Short-term protein restriction at advanced age stimulates FGF21 signalling, energy expenditure and browning of white adipose tissue

Marleen B. Dommerholt, Maaike Blankestijn, Marcel A. Vieira-Lara, Theo H. van Dijk, Henk Wolters, Mirjam H. Koster, Albert Gerding, Ronald P. van Os, Vincent W. Bloks, Barbara M. Bakker, Janine K. Kruit*, Johan W. Jonker

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Dietary protein restriction has been demonstrated to improve metabolic health under various conditions. However, the relevance of ageing and age-related decline in metabolic flexibility on the effects of dietary protein restriction has not been addressed. Therefore, we investigated the effect of short-term dietary protein restriction on metabolic health in young and aged mice. Young adult (3 months old) and aged (18 months old) C57Bl/6J mice were subjected to a 3-month dietary protein restriction. Outcome parameters included fibroblast growth factor 21 (FGF21) levels, muscle strength, glucose tolerance, energy expenditure (EE) and transcriptomics of brown and white adipose tissue (WAT). Here, we report that a low-protein diet had beneficial effects in aged mice by reducing some aspects of age-related metabolic decline. These effects were characterized by increased plasma levels of FGF21, browning of subcutaneous WAT, increased body temperature and EE, while no changes were observed in glucose homeostasis and insulin sensitivity. Moreover, the low-protein diet used in this study was well-tolerated in aged mice indicated by the absence of adverse effects on body weight, locomotor activity and muscle performance. In conclusion, our study demonstrates that a short-term reduction in dietary protein intake can impact age-related metabolic health alongside increased FGF21 signalling, without negatively affecting muscle function. These findings highlight the potential of protein restriction as a strategy to induce EE and browning of WAT in aged individuals.

Original languageEnglish
Pages (from-to)2257-2277
Number of pages21
JournalFEBS Journal
Volume288
Issue number7
Early online date22 Oct 2020
DOIs
Publication statusPublished - Apr 2021

Bibliographical note

Funding Information:
We thank Martijn Koehorst, Pim de Blaauw, Angelika Jurdzinski and Rick Havinga for excellent technical assistance, and Dicky Struik, Henkjan Verkade and Rebecca Heiner‐Fokkema for valuable feedback on the manuscript. This study was supported by an infrastructure grant from The Netherlands Organisation of Scientific Research (NWO): the Mouse Clinic for Cancer and Ageing (MCCA) and grants from The Netherlands Organization for Scientific Research (VICI grant 016.176.640 to JWJ), The Netherlands Organization for Scientific Research and the Dutch Diabetes Research Foundation (Diabetes II Breakthrough Project 459001005 to JKK), European Foundation for the Study of Diabetes (award supported by EFSD/Novo Nordisk to JWJ), a UMCG‐GSMS PhD fellowship to MAVL and the De Cock Stichting. The EE ANCOVA analysis done for this work was provided by the NIDDK Mouse Metabolic Phenotyping Centers (MMPC, www.mmpc.org ) using their EE Analysis page ( http://www.mmpc.org/shared/regression.aspx ) and supported by grants DK076169 and DK115255.

Publisher Copyright:
© 2020 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies

Funding

We thank Martijn Koehorst, Pim de Blaauw, Angelika Jurdzinski and Rick Havinga for excellent technical assistance, and Dicky Struik, Henkjan Verkade and Rebecca Heiner‐Fokkema for valuable feedback on the manuscript. This study was supported by an infrastructure grant from The Netherlands Organisation of Scientific Research (NWO): the Mouse Clinic for Cancer and Ageing (MCCA) and grants from The Netherlands Organization for Scientific Research (VICI grant 016.176.640 to JWJ), The Netherlands Organization for Scientific Research and the Dutch Diabetes Research Foundation (Diabetes II Breakthrough Project 459001005 to JKK), European Foundation for the Study of Diabetes (award supported by EFSD/Novo Nordisk to JWJ), a UMCG‐GSMS PhD fellowship to MAVL and the De Cock Stichting. The EE ANCOVA analysis done for this work was provided by the NIDDK Mouse Metabolic Phenotyping Centers (MMPC, www.mmpc.org ) using their EE Analysis page ( http://www.mmpc.org/shared/regression.aspx ) and supported by grants DK076169 and DK115255.

FundersFunder number
National Institute of Diabetes and Digestive and Kidney DiseasesDK076169, U24DK115255
European Foundation for the Study of Diabetes
Diabetes Fonds459001005
Nederlandse Organisatie voor Wetenschappelijk Onderzoek016.176.640
Novo Nordisk

    Keywords

    • browning of white adipose tissue
    • dietary protein restriction
    • energy metabolism
    • FGF21 signalling
    • thermogenesis

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