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Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles
Oxidative stress is associated with obstetric complications during ovarian hyperstimulation in women undergoing in vitro fertilization. The follicular fluid contains high levels of proteins, which are the main targets of free radicals. The aim of this work was to determine specific biomarkers of non...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315688/ https://www.ncbi.nlm.nih.gov/pubmed/30486406 http://dx.doi.org/10.3390/antiox7120176 |
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author | Pérez-Ruiz, Irantzu Meijide, Susana Hérnandez, María-Luisa Navarro, Rosaura Larreategui, Zaloa Ferrando, Marcos Ruiz-Larrea, María-Begoña Ruiz-Sanz, José-Ignacio |
author_facet | Pérez-Ruiz, Irantzu Meijide, Susana Hérnandez, María-Luisa Navarro, Rosaura Larreategui, Zaloa Ferrando, Marcos Ruiz-Larrea, María-Begoña Ruiz-Sanz, José-Ignacio |
author_sort | Pérez-Ruiz, Irantzu |
collection | PubMed |
description | Oxidative stress is associated with obstetric complications during ovarian hyperstimulation in women undergoing in vitro fertilization. The follicular fluid contains high levels of proteins, which are the main targets of free radicals. The aim of this work was to determine specific biomarkers of non-enzymatic oxidative modifications of proteins from follicular fluid in vivo, and the effect of ovarian stimulation with gonadotropins on these biomarkers. For this purpose, 27 fertile women underwent both a natural and a stimulated cycle. The biomarkers, glutamic semialdehyde (GSA), aminoadipic semialdehyde (AASA), N(ε)-(carboxymethyl)lysine (CML), and N(ε)-(carboxyethyl)lysine (CEL), were measured by gas-liquid chromatography coupled to mass spectrometry. Results showed that follicular fluid contained products of protein modifications by direct metal-catalyzed oxidation (GSA and AASA), glycoxidation (CML and CEL), and lipoxidation (CML). GSA was the most abundant biomarker (91.5%). The levels of CML amounted to 6% of the total lesions and were higher than AASA (1.3%) and CEL (1.2%). In the natural cycle, CEL was significantly lower (p < 0.05) than in the stimulated cycle, suggesting that natural cycles are more protected against protein glycoxidation. These findings are the basis for further research to elucidate the possible relevance of this follicular biomarker of advanced glycation end product in fertility programs. |
format | Online Article Text |
id | pubmed-6315688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63156882019-01-10 Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles Pérez-Ruiz, Irantzu Meijide, Susana Hérnandez, María-Luisa Navarro, Rosaura Larreategui, Zaloa Ferrando, Marcos Ruiz-Larrea, María-Begoña Ruiz-Sanz, José-Ignacio Antioxidants (Basel) Article Oxidative stress is associated with obstetric complications during ovarian hyperstimulation in women undergoing in vitro fertilization. The follicular fluid contains high levels of proteins, which are the main targets of free radicals. The aim of this work was to determine specific biomarkers of non-enzymatic oxidative modifications of proteins from follicular fluid in vivo, and the effect of ovarian stimulation with gonadotropins on these biomarkers. For this purpose, 27 fertile women underwent both a natural and a stimulated cycle. The biomarkers, glutamic semialdehyde (GSA), aminoadipic semialdehyde (AASA), N(ε)-(carboxymethyl)lysine (CML), and N(ε)-(carboxyethyl)lysine (CEL), were measured by gas-liquid chromatography coupled to mass spectrometry. Results showed that follicular fluid contained products of protein modifications by direct metal-catalyzed oxidation (GSA and AASA), glycoxidation (CML and CEL), and lipoxidation (CML). GSA was the most abundant biomarker (91.5%). The levels of CML amounted to 6% of the total lesions and were higher than AASA (1.3%) and CEL (1.2%). In the natural cycle, CEL was significantly lower (p < 0.05) than in the stimulated cycle, suggesting that natural cycles are more protected against protein glycoxidation. These findings are the basis for further research to elucidate the possible relevance of this follicular biomarker of advanced glycation end product in fertility programs. MDPI 2018-11-27 /pmc/articles/PMC6315688/ /pubmed/30486406 http://dx.doi.org/10.3390/antiox7120176 Text en © 2018 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 Pérez-Ruiz, Irantzu Meijide, Susana Hérnandez, María-Luisa Navarro, Rosaura Larreategui, Zaloa Ferrando, Marcos Ruiz-Larrea, María-Begoña Ruiz-Sanz, José-Ignacio Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles |
title | Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles |
title_full | Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles |
title_fullStr | Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles |
title_full_unstemmed | Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles |
title_short | Analysis of Protein Oxidative Modifications in Follicular Fluid from Fertile Women: Natural Versus Stimulated Cycles |
title_sort | analysis of protein oxidative modifications in follicular fluid from fertile women: natural versus stimulated cycles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315688/ https://www.ncbi.nlm.nih.gov/pubmed/30486406 http://dx.doi.org/10.3390/antiox7120176 |
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