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Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome
SHROB rats have been suggested as a model for metabolic syndrome (MetS) as a situation prior to the onset of CVD or type-2 diabetes, but information on descriptive biochemical parameters for this model is limited. Here, we extensively evaluate parameters related to CVD and oxidative stress (OS) in S...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4130542/ https://www.ncbi.nlm.nih.gov/pubmed/25115868 http://dx.doi.org/10.1371/journal.pone.0104637 |
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author | Molinar-Toribio, Eunice Pérez-Jiménez, Jara Ramos-Romero, Sara Lluís, Laura Sánchez-Martos, Vanessa Taltavull, Núria Romeu, Marta Pazos, Manuel Méndez, Lucía Miranda, Aníbal Cascante, Marta Medina, Isabel Torres, Josep Lluís |
author_facet | Molinar-Toribio, Eunice Pérez-Jiménez, Jara Ramos-Romero, Sara Lluís, Laura Sánchez-Martos, Vanessa Taltavull, Núria Romeu, Marta Pazos, Manuel Méndez, Lucía Miranda, Aníbal Cascante, Marta Medina, Isabel Torres, Josep Lluís |
author_sort | Molinar-Toribio, Eunice |
collection | PubMed |
description | SHROB rats have been suggested as a model for metabolic syndrome (MetS) as a situation prior to the onset of CVD or type-2 diabetes, but information on descriptive biochemical parameters for this model is limited. Here, we extensively evaluate parameters related to CVD and oxidative stress (OS) in SHROB rats. SHROB rats were monitored for 15 weeks and compared to a control group of Wistar rats. Body weight was recorded weekly. At the end of the study, parameters related to CVD and OS were evaluated in plasma, urine and different organs. SHROB rats presented statistically significant differences from Wistar rats in CVD risk factors: total cholesterol, LDL-cholesterol, triglycerides, apoA1, apoB100, abdominal fat, insulin, blood pressure, C-reactive protein, ICAM-1 and PAI-1. In adipose tissue, liver and brain, the endogenous antioxidant systems were activated, yet there was no significant oxidative damage to lipids (MDA) or proteins (carbonylation). We conclude that SHROB rats present significant alterations in parameters related to inflammation, endothelial dysfunction, thrombotic activity, insulin resistance and OS measured in plasma as well as enhanced redox defence systems in vital organs that will be useful as markers of MetS and CVD for nutrition interventions. |
format | Online Article Text |
id | pubmed-4130542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41305422014-08-14 Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome Molinar-Toribio, Eunice Pérez-Jiménez, Jara Ramos-Romero, Sara Lluís, Laura Sánchez-Martos, Vanessa Taltavull, Núria Romeu, Marta Pazos, Manuel Méndez, Lucía Miranda, Aníbal Cascante, Marta Medina, Isabel Torres, Josep Lluís PLoS One Research Article SHROB rats have been suggested as a model for metabolic syndrome (MetS) as a situation prior to the onset of CVD or type-2 diabetes, but information on descriptive biochemical parameters for this model is limited. Here, we extensively evaluate parameters related to CVD and oxidative stress (OS) in SHROB rats. SHROB rats were monitored for 15 weeks and compared to a control group of Wistar rats. Body weight was recorded weekly. At the end of the study, parameters related to CVD and OS were evaluated in plasma, urine and different organs. SHROB rats presented statistically significant differences from Wistar rats in CVD risk factors: total cholesterol, LDL-cholesterol, triglycerides, apoA1, apoB100, abdominal fat, insulin, blood pressure, C-reactive protein, ICAM-1 and PAI-1. In adipose tissue, liver and brain, the endogenous antioxidant systems were activated, yet there was no significant oxidative damage to lipids (MDA) or proteins (carbonylation). We conclude that SHROB rats present significant alterations in parameters related to inflammation, endothelial dysfunction, thrombotic activity, insulin resistance and OS measured in plasma as well as enhanced redox defence systems in vital organs that will be useful as markers of MetS and CVD for nutrition interventions. Public Library of Science 2014-08-12 /pmc/articles/PMC4130542/ /pubmed/25115868 http://dx.doi.org/10.1371/journal.pone.0104637 Text en © 2014 Molinar-Toribio 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Molinar-Toribio, Eunice Pérez-Jiménez, Jara Ramos-Romero, Sara Lluís, Laura Sánchez-Martos, Vanessa Taltavull, Núria Romeu, Marta Pazos, Manuel Méndez, Lucía Miranda, Aníbal Cascante, Marta Medina, Isabel Torres, Josep Lluís Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome |
title | Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome |
title_full | Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome |
title_fullStr | Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome |
title_full_unstemmed | Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome |
title_short | Cardiovascular Disease-Related Parameters and Oxidative Stress in SHROB Rats, a Model for Metabolic Syndrome |
title_sort | cardiovascular disease-related parameters and oxidative stress in shrob rats, a model for metabolic syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4130542/ https://www.ncbi.nlm.nih.gov/pubmed/25115868 http://dx.doi.org/10.1371/journal.pone.0104637 |
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