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Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose

Background. Continuous fructose consumption may cause elevation of circulating triacylglycerol. However, how much of this alteration is reverted after the removal of fructose intake is not known. We explored this question and compared the efficacy of this approach with fish oil supplementation. Meth...

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Autores principales: Sulis, Paola M., Motta, Katia, Barbosa, Amanda M., Besen, Matheus H., da Silva, Julia S., Nunes, Everson A., Rafacho, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591931/
https://www.ncbi.nlm.nih.gov/pubmed/28929113
http://dx.doi.org/10.1155/2017/4378328
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author Sulis, Paola M.
Motta, Katia
Barbosa, Amanda M.
Besen, Matheus H.
da Silva, Julia S.
Nunes, Everson A.
Rafacho, Alex
author_facet Sulis, Paola M.
Motta, Katia
Barbosa, Amanda M.
Besen, Matheus H.
da Silva, Julia S.
Nunes, Everson A.
Rafacho, Alex
author_sort Sulis, Paola M.
collection PubMed
description Background. Continuous fructose consumption may cause elevation of circulating triacylglycerol. However, how much of this alteration is reverted after the removal of fructose intake is not known. We explored this question and compared the efficacy of this approach with fish oil supplementation. Methods. Male Wistar rats were divided into the following groups: control (C), fructose (F) (water intake with 10% or 30% fructose for 9 weeks), fish oil (FO), and fructose/fish oil (FFO). Fish oil was supplemented only for the last 33 days of fructose ingestion. Half of the F group remained for additional 8 weeks without fructose ingestion (FR). Results. Fructose ingestion reduced food intake to compensate for the increased energy obtained through water ingestion, independent of fructose concentration. Fish oil supplementation exerted no impact on these parameters, but the removal of fructose from water recovered both ingestion behaviors. Plasma triacylglycerol augmented significantly during the second and third weeks (both fructose groups). Fish oil supplementation did not attenuate the elevation in triacylglycerol caused by fructose intake, but the interruption of sugar consumption normalized this parameter. Conclusion. Elevation in triacylglyceridemia may be recovered by removing fructose from diet, suggesting that it is never too late to repair improper dietary habits.
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spelling pubmed-55919312017-09-19 Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose Sulis, Paola M. Motta, Katia Barbosa, Amanda M. Besen, Matheus H. da Silva, Julia S. Nunes, Everson A. Rafacho, Alex Biomed Res Int Research Article Background. Continuous fructose consumption may cause elevation of circulating triacylglycerol. However, how much of this alteration is reverted after the removal of fructose intake is not known. We explored this question and compared the efficacy of this approach with fish oil supplementation. Methods. Male Wistar rats were divided into the following groups: control (C), fructose (F) (water intake with 10% or 30% fructose for 9 weeks), fish oil (FO), and fructose/fish oil (FFO). Fish oil was supplemented only for the last 33 days of fructose ingestion. Half of the F group remained for additional 8 weeks without fructose ingestion (FR). Results. Fructose ingestion reduced food intake to compensate for the increased energy obtained through water ingestion, independent of fructose concentration. Fish oil supplementation exerted no impact on these parameters, but the removal of fructose from water recovered both ingestion behaviors. Plasma triacylglycerol augmented significantly during the second and third weeks (both fructose groups). Fish oil supplementation did not attenuate the elevation in triacylglycerol caused by fructose intake, but the interruption of sugar consumption normalized this parameter. Conclusion. Elevation in triacylglyceridemia may be recovered by removing fructose from diet, suggesting that it is never too late to repair improper dietary habits. Hindawi 2017 2017-08-08 /pmc/articles/PMC5591931/ /pubmed/28929113 http://dx.doi.org/10.1155/2017/4378328 Text en Copyright © 2017 Paola M. Sulis et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sulis, Paola M.
Motta, Katia
Barbosa, Amanda M.
Besen, Matheus H.
da Silva, Julia S.
Nunes, Everson A.
Rafacho, Alex
Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose
title Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose
title_full Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose
title_fullStr Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose
title_full_unstemmed Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose
title_short Impact of Fish Oil Supplementation and Interruption of Fructose Ingestion on Glucose and Lipid Homeostasis of Rats Drinking Different Concentrations of Fructose
title_sort impact of fish oil supplementation and interruption of fructose ingestion on glucose and lipid homeostasis of rats drinking different concentrations of fructose
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591931/
https://www.ncbi.nlm.nih.gov/pubmed/28929113
http://dx.doi.org/10.1155/2017/4378328
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