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Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats

Mixtures of resveratrol (RSV) + quercetin (QRC) have antioxidant properties that probably impact on fatty liver in metabolic syndrome (MS) individuals. Here, we study the effects of a mixture of RSV + QRC on oxidative stress (OS) and fatty liver in a rat model of MS. Weanling male Wistar rats were s...

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Autores principales: Rubio-Ruiz, Maria Esther, Guarner-Lans, Verónica, Cano-Martínez, Agustina, Díaz-Díaz, Eulises, Manzano-Pech, Linaloe, Gamas-Magaña, Anel, Castrejón-Tellez, Vicente, Tapia-Cortina, Concepción, Pérez-Torres, Israel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479544/
https://www.ncbi.nlm.nih.gov/pubmed/30987086
http://dx.doi.org/10.3390/molecules24071297
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author Rubio-Ruiz, Maria Esther
Guarner-Lans, Verónica
Cano-Martínez, Agustina
Díaz-Díaz, Eulises
Manzano-Pech, Linaloe
Gamas-Magaña, Anel
Castrejón-Tellez, Vicente
Tapia-Cortina, Concepción
Pérez-Torres, Israel
author_facet Rubio-Ruiz, Maria Esther
Guarner-Lans, Verónica
Cano-Martínez, Agustina
Díaz-Díaz, Eulises
Manzano-Pech, Linaloe
Gamas-Magaña, Anel
Castrejón-Tellez, Vicente
Tapia-Cortina, Concepción
Pérez-Torres, Israel
author_sort Rubio-Ruiz, Maria Esther
collection PubMed
description Mixtures of resveratrol (RSV) + quercetin (QRC) have antioxidant properties that probably impact on fatty liver in metabolic syndrome (MS) individuals. Here, we study the effects of a mixture of RSV + QRC on oxidative stress (OS) and fatty liver in a rat model of MS. Weanling male Wistar rats were separated into four groups (n = 8): MS rats with 30% sucrose in drinking water plus RSV + QRC (50 and 0.95 mg/kg/day, respectively), MS rats without treatment, control rats (C), and C rats plus RSV + QRC. MS rats had increased systolic blood pressure, triglycerides, insulin levels, insulin resistance index homeostasis model (HOMA), adiponectin, and leptin. The RSV + QRC mixture compensated these variables to C values (p < 0.01) in MS rats. Lipid peroxidation and carbonylation were increased in MS. Total antioxidant capacity and glutathione (GSH) were decreased in MS and compensated in MS plus RVS + QRC rats. Catalase, superoxide dismutase isoforms, peroxidases, glutathione-S-transferase, glutathione reductase, and the expression of Nrf2 were decreased in MS and reversed in MS plus RVS + QRC rats (p < 0.01). In conclusion, the mixture of RSV + QRC has benefic effects on OS in fatty liver in the MS rats through the improvement of the antioxidant capacity and by the over-expression of the master factor Nrf2, which increases the antioxidant enzymes and GSH recycling.
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spelling pubmed-64795442019-04-30 Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats Rubio-Ruiz, Maria Esther Guarner-Lans, Verónica Cano-Martínez, Agustina Díaz-Díaz, Eulises Manzano-Pech, Linaloe Gamas-Magaña, Anel Castrejón-Tellez, Vicente Tapia-Cortina, Concepción Pérez-Torres, Israel Molecules Article Mixtures of resveratrol (RSV) + quercetin (QRC) have antioxidant properties that probably impact on fatty liver in metabolic syndrome (MS) individuals. Here, we study the effects of a mixture of RSV + QRC on oxidative stress (OS) and fatty liver in a rat model of MS. Weanling male Wistar rats were separated into four groups (n = 8): MS rats with 30% sucrose in drinking water plus RSV + QRC (50 and 0.95 mg/kg/day, respectively), MS rats without treatment, control rats (C), and C rats plus RSV + QRC. MS rats had increased systolic blood pressure, triglycerides, insulin levels, insulin resistance index homeostasis model (HOMA), adiponectin, and leptin. The RSV + QRC mixture compensated these variables to C values (p < 0.01) in MS rats. Lipid peroxidation and carbonylation were increased in MS. Total antioxidant capacity and glutathione (GSH) were decreased in MS and compensated in MS plus RVS + QRC rats. Catalase, superoxide dismutase isoforms, peroxidases, glutathione-S-transferase, glutathione reductase, and the expression of Nrf2 were decreased in MS and reversed in MS plus RVS + QRC rats (p < 0.01). In conclusion, the mixture of RSV + QRC has benefic effects on OS in fatty liver in the MS rats through the improvement of the antioxidant capacity and by the over-expression of the master factor Nrf2, which increases the antioxidant enzymes and GSH recycling. MDPI 2019-04-03 /pmc/articles/PMC6479544/ /pubmed/30987086 http://dx.doi.org/10.3390/molecules24071297 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rubio-Ruiz, Maria Esther
Guarner-Lans, Verónica
Cano-Martínez, Agustina
Díaz-Díaz, Eulises
Manzano-Pech, Linaloe
Gamas-Magaña, Anel
Castrejón-Tellez, Vicente
Tapia-Cortina, Concepción
Pérez-Torres, Israel
Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats
title Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats
title_full Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats
title_fullStr Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats
title_full_unstemmed Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats
title_short Resveratrol and Quercetin Administration Improves Antioxidant DEFENSES and reduces Fatty Liver in Metabolic Syndrome Rats
title_sort resveratrol and quercetin administration improves antioxidant defenses and reduces fatty liver in metabolic syndrome rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479544/
https://www.ncbi.nlm.nih.gov/pubmed/30987086
http://dx.doi.org/10.3390/molecules24071297
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