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β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle
The clinical benefit of ketosis has historically and almost exclusively centered on neurological conditions, lending insight into how ketones alter mitochondrial function in neurons. However, there is a gap in our understanding of how ketones influence mitochondria within skeletal muscle cells. The...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121962/ https://www.ncbi.nlm.nih.gov/pubmed/30071599 http://dx.doi.org/10.3390/ijms19082247 |
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author | Parker, Brian A. Walton, Chase M. Carr, Sheryl T. Andrus, Jacob L. Cheung, Eric C. K. Duplisea, Michael J. Wilson, Esther K. Draney, Carrie Lathen, Daniel R. Kenner, Kyle B. Thomson, David M. Tessem, Jeffery S. Bikman, Benjamin T. |
author_facet | Parker, Brian A. Walton, Chase M. Carr, Sheryl T. Andrus, Jacob L. Cheung, Eric C. K. Duplisea, Michael J. Wilson, Esther K. Draney, Carrie Lathen, Daniel R. Kenner, Kyle B. Thomson, David M. Tessem, Jeffery S. Bikman, Benjamin T. |
author_sort | Parker, Brian A. |
collection | PubMed |
description | The clinical benefit of ketosis has historically and almost exclusively centered on neurological conditions, lending insight into how ketones alter mitochondrial function in neurons. However, there is a gap in our understanding of how ketones influence mitochondria within skeletal muscle cells. The purpose of this study was to elucidate the specific effects of β-hydroxybutyrate (β-HB) on muscle cell mitochondrial physiology. In addition to increased cell viability, murine myotubes displayed beneficial mitochondrial changes evident in reduced H(2)O(2) emission and less mitochondrial fission, which may be a result of a β-HB-induced reduction in ceramides. Furthermore, muscle from rats in sustained ketosis similarly produced less H(2)O(2) despite an increase in mitochondrial respiration and no apparent change in mitochondrial quantity. In sum, these results indicate a general improvement in muscle cell mitochondrial function when β-HB is provided as a fuel. |
format | Online Article Text |
id | pubmed-6121962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61219622018-09-07 β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle Parker, Brian A. Walton, Chase M. Carr, Sheryl T. Andrus, Jacob L. Cheung, Eric C. K. Duplisea, Michael J. Wilson, Esther K. Draney, Carrie Lathen, Daniel R. Kenner, Kyle B. Thomson, David M. Tessem, Jeffery S. Bikman, Benjamin T. Int J Mol Sci Article The clinical benefit of ketosis has historically and almost exclusively centered on neurological conditions, lending insight into how ketones alter mitochondrial function in neurons. However, there is a gap in our understanding of how ketones influence mitochondria within skeletal muscle cells. The purpose of this study was to elucidate the specific effects of β-hydroxybutyrate (β-HB) on muscle cell mitochondrial physiology. In addition to increased cell viability, murine myotubes displayed beneficial mitochondrial changes evident in reduced H(2)O(2) emission and less mitochondrial fission, which may be a result of a β-HB-induced reduction in ceramides. Furthermore, muscle from rats in sustained ketosis similarly produced less H(2)O(2) despite an increase in mitochondrial respiration and no apparent change in mitochondrial quantity. In sum, these results indicate a general improvement in muscle cell mitochondrial function when β-HB is provided as a fuel. MDPI 2018-08-01 /pmc/articles/PMC6121962/ /pubmed/30071599 http://dx.doi.org/10.3390/ijms19082247 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Parker, Brian A. Walton, Chase M. Carr, Sheryl T. Andrus, Jacob L. Cheung, Eric C. K. Duplisea, Michael J. Wilson, Esther K. Draney, Carrie Lathen, Daniel R. Kenner, Kyle B. Thomson, David M. Tessem, Jeffery S. Bikman, Benjamin T. β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle |
title | β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle |
title_full | β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle |
title_fullStr | β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle |
title_full_unstemmed | β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle |
title_short | β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle |
title_sort | β-hydroxybutyrate elicits favorable mitochondrial changes in skeletal muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121962/ https://www.ncbi.nlm.nih.gov/pubmed/30071599 http://dx.doi.org/10.3390/ijms19082247 |
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