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Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats

BACKGROUND: Obesity is a primary factor of lifestyle-related diseases, and the age of its onset has decreased. The reactive oxygen species (ROS), the superoxide anion, is generated in the mitochondrial electron transport chain and the damage it induces in cells may be a contributing factor to obesit...

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Autores principales: Togo, M, Konari, N, Tsukamoto, M, Kimoto, R, Yamaguchi, T, Takeda, H, Kambayashi, I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853147/
https://www.ncbi.nlm.nih.gov/pubmed/29568243
http://dx.doi.org/10.1186/s12970-018-0217-z
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author Togo, M
Konari, N
Tsukamoto, M
Kimoto, R
Yamaguchi, T
Takeda, H
Kambayashi, I
author_facet Togo, M
Konari, N
Tsukamoto, M
Kimoto, R
Yamaguchi, T
Takeda, H
Kambayashi, I
author_sort Togo, M
collection PubMed
description BACKGROUND: Obesity is a primary factor of lifestyle-related diseases, and the age of its onset has decreased. The reactive oxygen species (ROS), the superoxide anion, is generated in the mitochondrial electron transport chain and the damage it induces in cells may be a contributing factor to obesity-related lifestyle diseases. In the present study, the influence of the ingestion of a high-fat diet (HFD) on superoxide anion generation in rat liver mitochondria (Mt) and membrane fluidity was investigated. METHODS: Male Wistar rats were fed a normal diet (ND, n = 6) or HFD (n = 6). Liver Mt were isolated and oxygen consumption, superoxide anion production (the adrenaline method), and membrane fluidity (the spin label method) were measured. RESULTS: After 11 weeks, body weights and abdominal circumferences were higher in the HFD group than in the ND group. Mt oxygen consumption was higher in the HFD group than in the ND group. Superoxide anion production was significantly lower in the HFD group than in the ND group, while no significant changes were observed in membrane fluidity. CONCLUSION: Although rats developed diet-induced obesity, it did not reach the level of disease development. The promotion of lipid metabolism appeared to reduce superoxide anion production, but did not influence membrane fluidity. While superoxide anion damages cells as an oxidative stress, ROS and superoxide dismutase are essential signaling molecules in the body. The present results suggest that the continuous ingestion of a HFD impairs Mt and induces disease development.
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spelling pubmed-58531472018-03-22 Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats Togo, M Konari, N Tsukamoto, M Kimoto, R Yamaguchi, T Takeda, H Kambayashi, I J Int Soc Sports Nutr Research Article BACKGROUND: Obesity is a primary factor of lifestyle-related diseases, and the age of its onset has decreased. The reactive oxygen species (ROS), the superoxide anion, is generated in the mitochondrial electron transport chain and the damage it induces in cells may be a contributing factor to obesity-related lifestyle diseases. In the present study, the influence of the ingestion of a high-fat diet (HFD) on superoxide anion generation in rat liver mitochondria (Mt) and membrane fluidity was investigated. METHODS: Male Wistar rats were fed a normal diet (ND, n = 6) or HFD (n = 6). Liver Mt were isolated and oxygen consumption, superoxide anion production (the adrenaline method), and membrane fluidity (the spin label method) were measured. RESULTS: After 11 weeks, body weights and abdominal circumferences were higher in the HFD group than in the ND group. Mt oxygen consumption was higher in the HFD group than in the ND group. Superoxide anion production was significantly lower in the HFD group than in the ND group, while no significant changes were observed in membrane fluidity. CONCLUSION: Although rats developed diet-induced obesity, it did not reach the level of disease development. The promotion of lipid metabolism appeared to reduce superoxide anion production, but did not influence membrane fluidity. While superoxide anion damages cells as an oxidative stress, ROS and superoxide dismutase are essential signaling molecules in the body. The present results suggest that the continuous ingestion of a HFD impairs Mt and induces disease development. BioMed Central 2018-03-14 /pmc/articles/PMC5853147/ /pubmed/29568243 http://dx.doi.org/10.1186/s12970-018-0217-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Togo, M
Konari, N
Tsukamoto, M
Kimoto, R
Yamaguchi, T
Takeda, H
Kambayashi, I
Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
title Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
title_full Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
title_fullStr Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
title_full_unstemmed Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
title_short Effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
title_sort effects of a high-fat diet on superoxide anion generation and membrane fluidity in liver mitochondria in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853147/
https://www.ncbi.nlm.nih.gov/pubmed/29568243
http://dx.doi.org/10.1186/s12970-018-0217-z
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