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NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN

Our data demonstrates that dietary protein restriction increases energy expenditure and improves glucose homeostasis, and that this effect is largely mediated by the metabolic hormone fibroblast growth factor 21(FGF21). Considering that the central nervous system (CNS) is acknowledged as a major reg...

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Autores principales: Hill, Cristal, Morrison, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6841317/
http://dx.doi.org/10.1093/geroni/igz038.2677
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author Hill, Cristal
Morrison, Christopher
author_facet Hill, Cristal
Morrison, Christopher
author_sort Hill, Cristal
collection PubMed
description Our data demonstrates that dietary protein restriction increases energy expenditure and improves glucose homeostasis, and that this effect is largely mediated by the metabolic hormone fibroblast growth factor 21(FGF21). Considering that the central nervous system (CNS) is acknowledged as a major regulator of both energy and glucose homeostasis, we have extended our studies to identify the tissue site mediating these FGF21-dependent effects via dietary protein restriction. In this study, mice with dysfunctional FGF21-signaling in either the CNS or adipose tissue were fed a control or low protein (LP)-diet to assess changes in body weight and metabolic endpoints. Our data show that LP diet increased energy expenditure and reduced body weight in control littermates, but these effects were lost in mice bearing CNS-specific deletion of Klb. These data highlight a liver to brain FGF21-signal as the first known neuroendocrine mechanism to explain the coordinated metabolic changes induced by dietary protein restriction.
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spelling pubmed-68413172019-11-13 NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN Hill, Cristal Morrison, Christopher Innov Aging Session 3385 (Symposium) Our data demonstrates that dietary protein restriction increases energy expenditure and improves glucose homeostasis, and that this effect is largely mediated by the metabolic hormone fibroblast growth factor 21(FGF21). Considering that the central nervous system (CNS) is acknowledged as a major regulator of both energy and glucose homeostasis, we have extended our studies to identify the tissue site mediating these FGF21-dependent effects via dietary protein restriction. In this study, mice with dysfunctional FGF21-signaling in either the CNS or adipose tissue were fed a control or low protein (LP)-diet to assess changes in body weight and metabolic endpoints. Our data show that LP diet increased energy expenditure and reduced body weight in control littermates, but these effects were lost in mice bearing CNS-specific deletion of Klb. These data highlight a liver to brain FGF21-signal as the first known neuroendocrine mechanism to explain the coordinated metabolic changes induced by dietary protein restriction. Oxford University Press 2019-11-08 /pmc/articles/PMC6841317/ http://dx.doi.org/10.1093/geroni/igz038.2677 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Session 3385 (Symposium)
Hill, Cristal
Morrison, Christopher
NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN
title NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN
title_full NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN
title_fullStr NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN
title_full_unstemmed NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN
title_short NEURONAL FGF-21 SIGNALING: A SENSOR OF DIETARY PROTEIN
title_sort neuronal fgf-21 signaling: a sensor of dietary protein
topic Session 3385 (Symposium)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6841317/
http://dx.doi.org/10.1093/geroni/igz038.2677
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