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Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster
Mitochondria can utilize different fuels according to physiological and nutritional conditions to promote cellular homeostasis. However, during nutrient overload metabolic inflexibility can occur, resulting in mitochondrial dysfunctions. High-fat diets (HFDs) are usually used to mimic this metabolic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418259/ https://www.ncbi.nlm.nih.gov/pubmed/30872605 http://dx.doi.org/10.1038/s41598-018-36060-5 |
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author | Cormier, Robert P. J. Champigny, Camille M. Simard, Chloé J. St-Coeur, Patrick-Denis Pichaud, Nicolas |
author_facet | Cormier, Robert P. J. Champigny, Camille M. Simard, Chloé J. St-Coeur, Patrick-Denis Pichaud, Nicolas |
author_sort | Cormier, Robert P. J. |
collection | PubMed |
description | Mitochondria can utilize different fuels according to physiological and nutritional conditions to promote cellular homeostasis. However, during nutrient overload metabolic inflexibility can occur, resulting in mitochondrial dysfunctions. High-fat diets (HFDs) are usually used to mimic this metabolic inflexibility in different animal models. However, how mitochondria respond to the duration of a HFD exposure is still under debate. In this study, we investigated the dynamic of the mitochondrial and physiological functions in Drosophila melanogaster at several time points following an exposure to a HFD. Our results showed that after two days on the HFD, mitochondrial respiration as well as ATP content of thorax muscles are increased, likely due to the utilization of carbohydrates. However, after four days on the HFD, impairment of mitochondrial respiration at the level of complex I, as well as decreased ATP content were observed. This was associated with an increased contribution of complex II and, most notably of the mitochondrial glycerol-3-phosphate dehydrogenase (mG3PDH) to mitochondrial respiration. We suggest that this increased mG3PDH capacity reflects the occurrence of metabolic inflexibility, leading to a loss of homeostasis and alteration of the cellular redox status, which results in senescence characterized by decreased climbing ability and premature death. |
format | Online Article Text |
id | pubmed-6418259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64182592019-03-18 Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster Cormier, Robert P. J. Champigny, Camille M. Simard, Chloé J. St-Coeur, Patrick-Denis Pichaud, Nicolas Sci Rep Article Mitochondria can utilize different fuels according to physiological and nutritional conditions to promote cellular homeostasis. However, during nutrient overload metabolic inflexibility can occur, resulting in mitochondrial dysfunctions. High-fat diets (HFDs) are usually used to mimic this metabolic inflexibility in different animal models. However, how mitochondria respond to the duration of a HFD exposure is still under debate. In this study, we investigated the dynamic of the mitochondrial and physiological functions in Drosophila melanogaster at several time points following an exposure to a HFD. Our results showed that after two days on the HFD, mitochondrial respiration as well as ATP content of thorax muscles are increased, likely due to the utilization of carbohydrates. However, after four days on the HFD, impairment of mitochondrial respiration at the level of complex I, as well as decreased ATP content were observed. This was associated with an increased contribution of complex II and, most notably of the mitochondrial glycerol-3-phosphate dehydrogenase (mG3PDH) to mitochondrial respiration. We suggest that this increased mG3PDH capacity reflects the occurrence of metabolic inflexibility, leading to a loss of homeostasis and alteration of the cellular redox status, which results in senescence characterized by decreased climbing ability and premature death. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418259/ /pubmed/30872605 http://dx.doi.org/10.1038/s41598-018-36060-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cormier, Robert P. J. Champigny, Camille M. Simard, Chloé J. St-Coeur, Patrick-Denis Pichaud, Nicolas Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster |
title | Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster |
title_full | Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster |
title_fullStr | Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster |
title_full_unstemmed | Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster |
title_short | Dynamic mitochondrial responses to a high-fat diet in Drosophila melanogaster |
title_sort | dynamic mitochondrial responses to a high-fat diet in drosophila melanogaster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418259/ https://www.ncbi.nlm.nih.gov/pubmed/30872605 http://dx.doi.org/10.1038/s41598-018-36060-5 |
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