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Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice

Mitochondrial dysfunction is widely reported in various diseases and contributes to their pathogenesis. We assessed the effect of cocoa flavanols supplementation on mitochondrial function and whole metabolism, and we explored whether the mitochondrial deacetylase sirtuin-3 (Sirt3) is involved or not...

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Autores principales: Daussin, Frédéric Nicolas, Cuillerier, Alexane, Touron, Julianne, Bensaid, Samir, Melo, Bruno, Al Rewashdy, Ali, Vasam, Goutham, Menzies, Keir J., Harper, Mary-Ellen, Heyman, Elsa, Burelle, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8538722/
https://www.ncbi.nlm.nih.gov/pubmed/34684467
http://dx.doi.org/10.3390/nu13103466
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author Daussin, Frédéric Nicolas
Cuillerier, Alexane
Touron, Julianne
Bensaid, Samir
Melo, Bruno
Al Rewashdy, Ali
Vasam, Goutham
Menzies, Keir J.
Harper, Mary-Ellen
Heyman, Elsa
Burelle, Yan
author_facet Daussin, Frédéric Nicolas
Cuillerier, Alexane
Touron, Julianne
Bensaid, Samir
Melo, Bruno
Al Rewashdy, Ali
Vasam, Goutham
Menzies, Keir J.
Harper, Mary-Ellen
Heyman, Elsa
Burelle, Yan
author_sort Daussin, Frédéric Nicolas
collection PubMed
description Mitochondrial dysfunction is widely reported in various diseases and contributes to their pathogenesis. We assessed the effect of cocoa flavanols supplementation on mitochondrial function and whole metabolism, and we explored whether the mitochondrial deacetylase sirtuin-3 (Sirt3) is involved or not. We explored the effects of 15 days of CF supplementation in wild type and Sirt3(-/-) mice. Whole-body metabolism was assessed by indirect calorimetry, and an oral glucose tolerance test was performed to assess glucose metabolism. Mitochondrial respiratory function was assessed in permeabilised fibres and the pyridine nucleotides content (NAD(+) and NADH) were quantified. In the wild type, CF supplementation significantly modified whole-body metabolism by promoting carbohydrate use and improved glucose tolerance. CF supplementation induced a significant increase of mitochondrial mass, while significant qualitative adaptation occurred to maintain H(2)O(2) production and cellular oxidative stress. CF supplementation induced a significant increase in NAD(+) and NADH content. All the effects mentioned above were blunted in Sirt3(-/-) mice. Collectively, CF supplementation boosted the NAD metabolism that stimulates sirtuins metabolism and improved mitochondrial function, which likely contributed to the observed whole-body metabolism adaptation, with a greater ability to use carbohydrates, at least partially through Sirt3.
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spelling pubmed-85387222021-10-24 Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice Daussin, Frédéric Nicolas Cuillerier, Alexane Touron, Julianne Bensaid, Samir Melo, Bruno Al Rewashdy, Ali Vasam, Goutham Menzies, Keir J. Harper, Mary-Ellen Heyman, Elsa Burelle, Yan Nutrients Article Mitochondrial dysfunction is widely reported in various diseases and contributes to their pathogenesis. We assessed the effect of cocoa flavanols supplementation on mitochondrial function and whole metabolism, and we explored whether the mitochondrial deacetylase sirtuin-3 (Sirt3) is involved or not. We explored the effects of 15 days of CF supplementation in wild type and Sirt3(-/-) mice. Whole-body metabolism was assessed by indirect calorimetry, and an oral glucose tolerance test was performed to assess glucose metabolism. Mitochondrial respiratory function was assessed in permeabilised fibres and the pyridine nucleotides content (NAD(+) and NADH) were quantified. In the wild type, CF supplementation significantly modified whole-body metabolism by promoting carbohydrate use and improved glucose tolerance. CF supplementation induced a significant increase of mitochondrial mass, while significant qualitative adaptation occurred to maintain H(2)O(2) production and cellular oxidative stress. CF supplementation induced a significant increase in NAD(+) and NADH content. All the effects mentioned above were blunted in Sirt3(-/-) mice. Collectively, CF supplementation boosted the NAD metabolism that stimulates sirtuins metabolism and improved mitochondrial function, which likely contributed to the observed whole-body metabolism adaptation, with a greater ability to use carbohydrates, at least partially through Sirt3. MDPI 2021-09-29 /pmc/articles/PMC8538722/ /pubmed/34684467 http://dx.doi.org/10.3390/nu13103466 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Daussin, Frédéric Nicolas
Cuillerier, Alexane
Touron, Julianne
Bensaid, Samir
Melo, Bruno
Al Rewashdy, Ali
Vasam, Goutham
Menzies, Keir J.
Harper, Mary-Ellen
Heyman, Elsa
Burelle, Yan
Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice
title Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice
title_full Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice
title_fullStr Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice
title_full_unstemmed Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice
title_short Dietary Cocoa Flavanols Enhance Mitochondrial Function in Skeletal Muscle and Modify Whole-Body Metabolism in Healthy Mice
title_sort dietary cocoa flavanols enhance mitochondrial function in skeletal muscle and modify whole-body metabolism in healthy mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8538722/
https://www.ncbi.nlm.nih.gov/pubmed/34684467
http://dx.doi.org/10.3390/nu13103466
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