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Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis

The present study evaluated the cardiometabolic and redox balance profiles in patients with Metabolic Syndrome compared to apparently healthy individuals, and the participation of the myeloperoxidase/hydrogen peroxide axis in systemic lipid peroxidation. Twenty-four patients with Metabolic Syndrome...

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Autores principales: da Fonseca, Lucas José Sá, Nunes-Souza, Valéria, Guedes, Glaucevane da Silva, Schettino-Silva, Glauber, Mota-Gomes, Marco Antônio, Rabelo, Luíza Antas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216703/
https://www.ncbi.nlm.nih.gov/pubmed/25386227
http://dx.doi.org/10.1155/2014/898501
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author da Fonseca, Lucas José Sá
Nunes-Souza, Valéria
Guedes, Glaucevane da Silva
Schettino-Silva, Glauber
Mota-Gomes, Marco Antônio
Rabelo, Luíza Antas
author_facet da Fonseca, Lucas José Sá
Nunes-Souza, Valéria
Guedes, Glaucevane da Silva
Schettino-Silva, Glauber
Mota-Gomes, Marco Antônio
Rabelo, Luíza Antas
author_sort da Fonseca, Lucas José Sá
collection PubMed
description The present study evaluated the cardiometabolic and redox balance profiles in patients with Metabolic Syndrome compared to apparently healthy individuals, and the participation of the myeloperoxidase/hydrogen peroxide axis in systemic lipid peroxidation. Twenty-four patients with Metabolic Syndrome and eighteen controls underwent a full clinical assessment. Venous blood samples were collected for general biochemical dosages, as well as for the oxidative stress analyses (superoxide dismutase, catalase, and arginase activities; and lipid peroxidation, myeloperoxidase activity, nitrite, and hydrogen peroxide concentrations in plasma). Arterial stiffness was assessed by radial artery applanation tonometry. Plasma lipid peroxidation, erythrocyte superoxide dismutase activity, myeloperoxidase activity, and hydrogen peroxide concentrations were shown to be increased in Metabolic Syndrome patients, without significant differences for the other enzymes, plasma nitrite concentrations, and arterial stiffness. Linear regression analysis revealed a positive and significant correlation between lipid peroxidation and myeloperoxidase and also between this enzyme and hydrogen peroxide. In contrast, such correlation was not observed between lipid peroxidation and hydrogen peroxide. In summary, Metabolic Syndrome patients exhibited evident systemic redox imbalance compared to controls, with the possible participation of the myeloperoxidase/hydrogen peroxide axis as a contributor in lipid peroxidation.
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spelling pubmed-42167032014-11-10 Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis da Fonseca, Lucas José Sá Nunes-Souza, Valéria Guedes, Glaucevane da Silva Schettino-Silva, Glauber Mota-Gomes, Marco Antônio Rabelo, Luíza Antas Oxid Med Cell Longev Clinical Study The present study evaluated the cardiometabolic and redox balance profiles in patients with Metabolic Syndrome compared to apparently healthy individuals, and the participation of the myeloperoxidase/hydrogen peroxide axis in systemic lipid peroxidation. Twenty-four patients with Metabolic Syndrome and eighteen controls underwent a full clinical assessment. Venous blood samples were collected for general biochemical dosages, as well as for the oxidative stress analyses (superoxide dismutase, catalase, and arginase activities; and lipid peroxidation, myeloperoxidase activity, nitrite, and hydrogen peroxide concentrations in plasma). Arterial stiffness was assessed by radial artery applanation tonometry. Plasma lipid peroxidation, erythrocyte superoxide dismutase activity, myeloperoxidase activity, and hydrogen peroxide concentrations were shown to be increased in Metabolic Syndrome patients, without significant differences for the other enzymes, plasma nitrite concentrations, and arterial stiffness. Linear regression analysis revealed a positive and significant correlation between lipid peroxidation and myeloperoxidase and also between this enzyme and hydrogen peroxide. In contrast, such correlation was not observed between lipid peroxidation and hydrogen peroxide. In summary, Metabolic Syndrome patients exhibited evident systemic redox imbalance compared to controls, with the possible participation of the myeloperoxidase/hydrogen peroxide axis as a contributor in lipid peroxidation. Hindawi Publishing Corporation 2014 2014-10-15 /pmc/articles/PMC4216703/ /pubmed/25386227 http://dx.doi.org/10.1155/2014/898501 Text en Copyright © 2014 Lucas José Sá da Fonseca et al. https://creativecommons.org/licenses/by/3.0/ 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 Clinical Study
da Fonseca, Lucas José Sá
Nunes-Souza, Valéria
Guedes, Glaucevane da Silva
Schettino-Silva, Glauber
Mota-Gomes, Marco Antônio
Rabelo, Luíza Antas
Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis
title Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis
title_full Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis
title_fullStr Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis
title_full_unstemmed Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis
title_short Oxidative Status Imbalance in Patients with Metabolic Syndrome: Role of the Myeloperoxidase/Hydrogen Peroxide Axis
title_sort oxidative status imbalance in patients with metabolic syndrome: role of the myeloperoxidase/hydrogen peroxide axis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216703/
https://www.ncbi.nlm.nih.gov/pubmed/25386227
http://dx.doi.org/10.1155/2014/898501
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