Cargando…

Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle

Purpose: Ketone bodies are energy substrates produced by the liver during prolonged fasting or low-carbohydrate diet. The ingestion of a ketone ester (KE) rapidly increases blood ketone levels independent of nutritional status. KE has recently been shown to improve exercise performance, but whether...

Descripción completa

Detalles Bibliográficos
Autores principales: Vandoorne, Tijs, De Smet, Stefan, Ramaekers, Monique, Van Thienen, Ruud, De Bock, Katrien, Clarke, Kieran, Hespel, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440563/
https://www.ncbi.nlm.nih.gov/pubmed/28588499
http://dx.doi.org/10.3389/fphys.2017.00310
_version_ 1783238086230016000
author Vandoorne, Tijs
De Smet, Stefan
Ramaekers, Monique
Van Thienen, Ruud
De Bock, Katrien
Clarke, Kieran
Hespel, Peter
author_facet Vandoorne, Tijs
De Smet, Stefan
Ramaekers, Monique
Van Thienen, Ruud
De Bock, Katrien
Clarke, Kieran
Hespel, Peter
author_sort Vandoorne, Tijs
collection PubMed
description Purpose: Ketone bodies are energy substrates produced by the liver during prolonged fasting or low-carbohydrate diet. The ingestion of a ketone ester (KE) rapidly increases blood ketone levels independent of nutritional status. KE has recently been shown to improve exercise performance, but whether it can also promote post-exercise muscle protein or glycogen synthesis is unknown. Methods: Eight healthy trained males participated in a randomized double-blind placebo-controlled crossover study. In each session, subjects undertook a bout of intense one-leg glycogen-depleting exercise followed by a 5-h recovery period during which they ingested a protein/carbohydrate mixture. Additionally, subjects ingested a ketone ester (KE) or an isocaloric placebo (PL). Results: KE intake did not affect muscle glycogen resynthesis, but more rapidly lowered post-exercise AMPK phosphorylation and resulted in higher mTORC1 activation, as evidenced by the higher phosphorylation of its main downstream targets S6K1 and 4E-BP1. As enhanced mTORC1 activation following KE suggests higher protein synthesis rates, we used myogenic C(2)C(12) cells to further confirm that ketone bodies increase both leucine-mediated mTORC1 activation and protein synthesis in muscle cells. Conclusion: Our results indicate that adding KE to a standard post-exercise recovery beverage enhances the post-exercise activation of mTORC1 but does not affect muscle glycogen resynthesis in young healthy volunteers. In vitro, we confirmed that ketone bodies potentiate the increase in mTORC1 activation and protein synthesis in leucine-stimulated myotubes. Whether, chronic oral KE intake during recovery from exercise can facilitate training-induced muscular adaptation and remodeling need to be further investigated.
format Online
Article
Text
id pubmed-5440563
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-54405632017-06-06 Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle Vandoorne, Tijs De Smet, Stefan Ramaekers, Monique Van Thienen, Ruud De Bock, Katrien Clarke, Kieran Hespel, Peter Front Physiol Physiology Purpose: Ketone bodies are energy substrates produced by the liver during prolonged fasting or low-carbohydrate diet. The ingestion of a ketone ester (KE) rapidly increases blood ketone levels independent of nutritional status. KE has recently been shown to improve exercise performance, but whether it can also promote post-exercise muscle protein or glycogen synthesis is unknown. Methods: Eight healthy trained males participated in a randomized double-blind placebo-controlled crossover study. In each session, subjects undertook a bout of intense one-leg glycogen-depleting exercise followed by a 5-h recovery period during which they ingested a protein/carbohydrate mixture. Additionally, subjects ingested a ketone ester (KE) or an isocaloric placebo (PL). Results: KE intake did not affect muscle glycogen resynthesis, but more rapidly lowered post-exercise AMPK phosphorylation and resulted in higher mTORC1 activation, as evidenced by the higher phosphorylation of its main downstream targets S6K1 and 4E-BP1. As enhanced mTORC1 activation following KE suggests higher protein synthesis rates, we used myogenic C(2)C(12) cells to further confirm that ketone bodies increase both leucine-mediated mTORC1 activation and protein synthesis in muscle cells. Conclusion: Our results indicate that adding KE to a standard post-exercise recovery beverage enhances the post-exercise activation of mTORC1 but does not affect muscle glycogen resynthesis in young healthy volunteers. In vitro, we confirmed that ketone bodies potentiate the increase in mTORC1 activation and protein synthesis in leucine-stimulated myotubes. Whether, chronic oral KE intake during recovery from exercise can facilitate training-induced muscular adaptation and remodeling need to be further investigated. Frontiers Media S.A. 2017-05-23 /pmc/articles/PMC5440563/ /pubmed/28588499 http://dx.doi.org/10.3389/fphys.2017.00310 Text en Copyright © 2017 Vandoorne, De Smet, Ramaekers, Van Thienen, De Bock, Clarke and Hespel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Vandoorne, Tijs
De Smet, Stefan
Ramaekers, Monique
Van Thienen, Ruud
De Bock, Katrien
Clarke, Kieran
Hespel, Peter
Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle
title Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle
title_full Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle
title_fullStr Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle
title_full_unstemmed Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle
title_short Intake of a Ketone Ester Drink during Recovery from Exercise Promotes mTORC1 Signaling but Not Glycogen Resynthesis in Human Muscle
title_sort intake of a ketone ester drink during recovery from exercise promotes mtorc1 signaling but not glycogen resynthesis in human muscle
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440563/
https://www.ncbi.nlm.nih.gov/pubmed/28588499
http://dx.doi.org/10.3389/fphys.2017.00310
work_keys_str_mv AT vandoornetijs intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle
AT desmetstefan intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle
AT ramaekersmonique intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle
AT vanthienenruud intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle
AT debockkatrien intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle
AT clarkekieran intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle
AT hespelpeter intakeofaketoneesterdrinkduringrecoveryfromexercisepromotesmtorc1signalingbutnotglycogenresynthesisinhumanmuscle