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ß-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.
Afiliação
  • Parker BA; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. info@youarelimitless.org.
  • Walton CM; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. chase.m.walton@gmail.com.
  • Carr ST; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. sherylteresa@gmail.com.
  • Andrus JL; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. jacob.l.andrus@gmail.com.
  • Cheung ECK; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. eric.cheung.801@gmail.com.
  • Duplisea MJ; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. mduplisea@hotmail.com.
  • Wilson EK; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. olsenkezia@gmail.com.
  • Draney C; Department of Nutrition, Dietetics and Food Science, Brigham Young University, Provo, UT 84604, USA. carriedraney@gmail.com.
  • Lathen DR; Department of Nutrition, Dietetics and Food Science, Brigham Young University, Provo, UT 84604, USA. drlathen@gmail.com.
  • Kenner KB; Department of Nutrition, Dietetics and Food Science, Brigham Young University, Provo, UT 84604, USA. kyle.kener@gmail.com.
  • Thomson DM; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. david_thomson@byu.edu.
  • Tessem JS; Department of Nutrition, Dietetics and Food Science, Brigham Young University, Provo, UT 84604, USA. jeffery_tessem@byu.edu.
  • Bikman BT; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84604, USA. benjamin_bikman@byu.edu.
Int J Mol Sci ; 19(8)2018 Aug 01.
Article em En | MEDLINE | ID: mdl-30071599
ABSTRACT
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 ß-hydroxybutyrate (ß-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 ß-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 ß-HB is provided as a fuel.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Consumo de Oxigênio / Ceramidas / Músculo Esquelético / Ácido 3-Hidroxibutírico / Mitocôndrias Musculares Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Consumo de Oxigênio / Ceramidas / Músculo Esquelético / Ácido 3-Hidroxibutírico / Mitocôndrias Musculares Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos