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β-Hydroxybutyrate Elicits Favorable Mitochondrial Changes in Skeletal Muscle.

Brian A Parker | Chase M Walton | Sheryl T Carr | Jacob L Andrus | Eric C K Cheung | Michael J Duplisea | Esther K Wilson | Carrie Draney | Daniel R Lathen | Kyle B Kenner | David M Thomson | Jeffery S Tessem | Benjamin T Bikman
International journal of molecular sciences | 2018

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 H₂O₂ 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 H₂O₂ 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.

Pubmed ID: 30071599

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