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High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans
Glucose is an important nutrient that dictates the development, fertility and lifespan of all organisms. In humans, a deficit in its homeostatic control might lead to hyperglucemia and the development of obesity and type 2 diabetes, which show a decreased ability to respond to and metabolize glucose...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917275/ https://www.ncbi.nlm.nih.gov/pubmed/31846489 http://dx.doi.org/10.1371/journal.pone.0226652 |
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author | Alcántar-Fernández, Jonathan González-Maciel, Angélica Reynoso-Robles, Rafael Pérez Andrade, Martha Elva Hernández-Vázquez, Alain de J. Velázquez-Arellano, Antonio Miranda-Ríos, Juan |
author_facet | Alcántar-Fernández, Jonathan González-Maciel, Angélica Reynoso-Robles, Rafael Pérez Andrade, Martha Elva Hernández-Vázquez, Alain de J. Velázquez-Arellano, Antonio Miranda-Ríos, Juan |
author_sort | Alcántar-Fernández, Jonathan |
collection | PubMed |
description | Glucose is an important nutrient that dictates the development, fertility and lifespan of all organisms. In humans, a deficit in its homeostatic control might lead to hyperglucemia and the development of obesity and type 2 diabetes, which show a decreased ability to respond to and metabolize glucose. Previously, we have reported that high-glucose diets (HGD) induce alterations in triglyceride content, body size, progeny, and the mRNA accumulation of key regulators of carbohydrate and lipid metabolism, and longevity in Caenorhabditis elegans (PLoS ONE 13(7): e0199888). Herein, we show that increasing amounts of glucose in the diet induce the swelling of both mitochondria in germ and muscle cells. Additionally, HGD alter the enzymatic activities of the different respiratory complexes in an intricate pattern. Finally, we observed a downregulation of ceramide synthases (hyl-1 and hyl-2) and antioxidant genes (gcs-1 and gst-4), while mitophagy genes (pink-1 and dct-1) were upregulated, probably as part of a mitohormetic mechanism in response to glucose toxicity. |
format | Online Article Text |
id | pubmed-6917275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69172752019-12-27 High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans Alcántar-Fernández, Jonathan González-Maciel, Angélica Reynoso-Robles, Rafael Pérez Andrade, Martha Elva Hernández-Vázquez, Alain de J. Velázquez-Arellano, Antonio Miranda-Ríos, Juan PLoS One Research Article Glucose is an important nutrient that dictates the development, fertility and lifespan of all organisms. In humans, a deficit in its homeostatic control might lead to hyperglucemia and the development of obesity and type 2 diabetes, which show a decreased ability to respond to and metabolize glucose. Previously, we have reported that high-glucose diets (HGD) induce alterations in triglyceride content, body size, progeny, and the mRNA accumulation of key regulators of carbohydrate and lipid metabolism, and longevity in Caenorhabditis elegans (PLoS ONE 13(7): e0199888). Herein, we show that increasing amounts of glucose in the diet induce the swelling of both mitochondria in germ and muscle cells. Additionally, HGD alter the enzymatic activities of the different respiratory complexes in an intricate pattern. Finally, we observed a downregulation of ceramide synthases (hyl-1 and hyl-2) and antioxidant genes (gcs-1 and gst-4), while mitophagy genes (pink-1 and dct-1) were upregulated, probably as part of a mitohormetic mechanism in response to glucose toxicity. Public Library of Science 2019-12-17 /pmc/articles/PMC6917275/ /pubmed/31846489 http://dx.doi.org/10.1371/journal.pone.0226652 Text en © 2019 Alcántar-Fernández et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Alcántar-Fernández, Jonathan González-Maciel, Angélica Reynoso-Robles, Rafael Pérez Andrade, Martha Elva Hernández-Vázquez, Alain de J. Velázquez-Arellano, Antonio Miranda-Ríos, Juan High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
title | High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
title_full | High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
title_fullStr | High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
title_full_unstemmed | High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
title_short | High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
title_sort | high-glucose diets induce mitochondrial dysfunction in caenorhabditis elegans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917275/ https://www.ncbi.nlm.nih.gov/pubmed/31846489 http://dx.doi.org/10.1371/journal.pone.0226652 |
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