Parameters of Oxidative Stress in Reproductive and Postmenopausal Mexican Women

In the reproductive phase, women experience cyclic changes in the ovaries and uterus, and hormones regulate these changes. Menopause is the permanent loss of menstruation after 12 months of amenorrhea. Menopause is also linked to a decrease in estrogen production, causing an imbalance in oxidative s...

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Published in:International journal of environmental research and public health Vol. 17; no. 5; p. 1492
Main Authors: Montoya-Estrada, Araceli, Velázquez-Yescas, Karla Guadalupe, Veruete-Bedolla, Daniela Belen, Ruiz-Herrera, José David, Villarreal-Barranca, Alma, Romo-Yañez, José, Ortiz-Luna, Guillermo Federico, Arellano-Eguiluz, Arturo, Solis-Paredes, Mario, Flores-Pliego, Arturo, Espejel-Nuñez, Aurora, Estrada-Gutierrez, Guadalupe, Reyes-Muñoz, Enrique
Format: Journal Article
Language:English
Published: Switzerland MDPI 26-02-2020
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Summary:In the reproductive phase, women experience cyclic changes in the ovaries and uterus, and hormones regulate these changes. Menopause is the permanent loss of menstruation after 12 months of amenorrhea. Menopause is also linked to a decrease in estrogen production, causing an imbalance in oxidative stress. We aimed to compare the three stages of lipid peroxidation, protein oxidative damage, and total antioxidant capacity (TAC) between reproductive-aged women (RAW) and postmenopausal women (PMW) in Mexico. We carried out a cross-sectional study with 84 women from Mexico City, including 40 RAW and 44 PMW. To determine the oxidative stress of the participants, several markers of lipid damage were measured: dienes conjugates (DC), lipohydroperoxides (LHP), and malondialdehyde (MDA); exposure to protein carbonyl is indicative of oxidative modified proteins, and TAC is indicative of the antioxidant defense system. Biomarkers of oxidative stress were significantly lower in RAW vs. PMW. DC were 1.31 ± 0.65 vs. 1.7 ± 0.51 pmol DC/mg dry weight ( = 0.0032); LHP were 4.95 ± 2.20 vs. 11.30 ± 4.24 pmol LHP/mg dry weight ( < 0.0001); malondialdehyde was 20.37 ± 8.20 vs. 26.10 ± 8.71 pmol MDA/mg dry weight ( = 0.0030); exposure of protein carbonyl was 3954 ± 884 vs. 4552 ± 1445 pmol PC/mg protein ( = 0.042); and TAC was 7244 ± 1512 vs. 8099 ± 1931 pmol Trolox equivalent/mg protein ( = 0.027). PMW display significantly higher oxidative stress markers compared to RAW; likewise, PMW show a higher TAC.
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ISSN:1660-4601
1661-7827
1660-4601
DOI:10.3390/ijerph17051492