Cardiovascular disease-related parameters and Oxidative stress in SHROB rats, a model for metabolic syndrome.

dc.contributor.authorMolinar Toribio, Eunice María
dc.contributor.authorPérez-Jiménez, Jara
dc.contributor.authorRamos Romero, Sara
dc.contributor.authorLluís, Laura
dc.contributor.authorSánchez-Martos, Vanessa
dc.contributor.authorTaltavull, Núria
dc.contributor.authorRomeu Ferran, Marta
dc.contributor.authorPazos, Manuel
dc.contributor.authorMéndez, Lucía
dc.contributor.authorMiranda, Aníbal
dc.contributor.authorCascante i Serratosa, Marta
dc.contributor.authorMedina, Isabel
dc.contributor.authorTorres, Josep Lluís
dc.date.accessioned2014-10-30T14:25:09Z
dc.date.available2014-10-30T14:25:09Z
dc.date.issued2014-08-12
dc.date.updated2014-10-30T14:25:09Z
dc.description.abstractSHROB 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.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec644066
dc.identifier.issn1932-6203
dc.identifier.pmid25115868
dc.identifier.urihttps://hdl.handle.net/2445/59234
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0104637
dc.relation.ispartofPLoS One, 2014, vol. 9, num. 8
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/222639/EU//ETHERPATHS
dc.relation.urihttp://dx.doi.org/10.1371/journal.pone.0104637
dc.rightscc-by (c) Molinar-Toribio, E. et al., 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Bioquímica i Biomedicina Molecular)
dc.subject.classificationInfermeria cardiovascular
dc.subject.classificationEstrès oxidatiu
dc.subject.classificationSíndrome metabòlica
dc.subject.otherCardiovascular disease nursing
dc.subject.otherOxidative stress
dc.subject.otherMetabolic syndrome
dc.titleCardiovascular disease-related parameters and Oxidative stress in SHROB rats, a model for metabolic syndrome.
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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