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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6479544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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