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Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility

The intensification of oxidative stress and destabilization of the antioxidative defenses of an organism is a consequence of many environmental factors. We considered aspects conditioning male reproductive potential and the functionality of enzymatic antioxidative mechanisms, i.e., superoxide dismut...

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Autores principales: Baszyński, Jędrzej, Kamiński, Piotr, Bogdzińska, Maria, Mroczkowski, Sławomir, Szymański, Marek, Wasilow, Karolina, Stanek, Emilia, Hołderna-Bona, Karolina, Brodzka, Sylwia, Bilski, Rafał, Tkachenko, Halyna, Kurhaluk, Natalia, Stuczyński, Tomasz, Lorek, Małgorzata, Woźniak, Alina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138092/
https://www.ncbi.nlm.nih.gov/pubmed/35624681
http://dx.doi.org/10.3390/antiox11050817
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author Baszyński, Jędrzej
Kamiński, Piotr
Bogdzińska, Maria
Mroczkowski, Sławomir
Szymański, Marek
Wasilow, Karolina
Stanek, Emilia
Hołderna-Bona, Karolina
Brodzka, Sylwia
Bilski, Rafał
Tkachenko, Halyna
Kurhaluk, Natalia
Stuczyński, Tomasz
Lorek, Małgorzata
Woźniak, Alina
author_facet Baszyński, Jędrzej
Kamiński, Piotr
Bogdzińska, Maria
Mroczkowski, Sławomir
Szymański, Marek
Wasilow, Karolina
Stanek, Emilia
Hołderna-Bona, Karolina
Brodzka, Sylwia
Bilski, Rafał
Tkachenko, Halyna
Kurhaluk, Natalia
Stuczyński, Tomasz
Lorek, Małgorzata
Woźniak, Alina
author_sort Baszyński, Jędrzej
collection PubMed
description The intensification of oxidative stress and destabilization of the antioxidative defenses of an organism is a consequence of many environmental factors. We considered aspects conditioning male reproductive potential and the functionality of enzymatic antioxidative mechanisms, i.e., superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and glutathione reductase (GR), and their correlations with Li, Be, B, Na, Mg, Al, P, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Sr, Mo, Ag, Cd, Sn, Sb, Ba, Hg, Tl, Pb, and malondialdehyde (MDA), as well as genetic polymorphism IL-4v.C589T (rs2243250) in men with infertility (n = 76). A healthy normozoospermic control (n = 87) was also used. We assessed the impact of negative changes driven by oxidative stress on enzymatic antioxidative mechanisms as well as the role of MDA in the overall process. On this basis, we infer connections between disturbances in enzymatic antioxidative defense and reproductive potential. Based on a molecular analysis of the polymorphism of gene IL-4v.C589T (rs2243250) (chromosome 5) (PCR-RFLP), we considered the relationships among particular genotypes with the possibility of occurrence of male infertility. Concentrations of chemical elements were measured in the blood. The activity of antioxidants and MDA levels were measured in serum. In the infertile group, higher GPx activity was noted (6.56 nmoL·min(−1)·mL(−1), control: 4.31 nmoL·min(−1)·mL(−1); p = 0.004), while GR achieved a greater level in the control (17.74 nmoL·min(−1)·mL(−1), infertile: 15.97 nmoL·min(−1)·mL(−1), p = 0.043), which implies diversified efficiency of the first and second lines of defense. The polymorphism of IL-4v.C589T (rs2243250) was not directly connected with infertility because there were not any differences in the frequency of genotypes between the infertile and control group (p = 0.578). An analysis of genotypes CC and TT (polymorphism IL-4v.C589T (rs2243250)) indicated numerous correlations between antioxidants, chemical elements and MDA. Therefore, chemical economy, antioxidative defense and genetic conditions are connected and jointly shape male reproductive potential. Chemical elements influence antioxidative defense and male fertility; the most important modulators appeared to be Na, Ba, Al and B. The polymorphism of gene IL-4v.C589T (rs2243250) has a limited influence on antioxidative defense and the metabolism of chemical elements.
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spelling pubmed-91380922022-05-28 Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility Baszyński, Jędrzej Kamiński, Piotr Bogdzińska, Maria Mroczkowski, Sławomir Szymański, Marek Wasilow, Karolina Stanek, Emilia Hołderna-Bona, Karolina Brodzka, Sylwia Bilski, Rafał Tkachenko, Halyna Kurhaluk, Natalia Stuczyński, Tomasz Lorek, Małgorzata Woźniak, Alina Antioxidants (Basel) Article The intensification of oxidative stress and destabilization of the antioxidative defenses of an organism is a consequence of many environmental factors. We considered aspects conditioning male reproductive potential and the functionality of enzymatic antioxidative mechanisms, i.e., superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and glutathione reductase (GR), and their correlations with Li, Be, B, Na, Mg, Al, P, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Sr, Mo, Ag, Cd, Sn, Sb, Ba, Hg, Tl, Pb, and malondialdehyde (MDA), as well as genetic polymorphism IL-4v.C589T (rs2243250) in men with infertility (n = 76). A healthy normozoospermic control (n = 87) was also used. We assessed the impact of negative changes driven by oxidative stress on enzymatic antioxidative mechanisms as well as the role of MDA in the overall process. On this basis, we infer connections between disturbances in enzymatic antioxidative defense and reproductive potential. Based on a molecular analysis of the polymorphism of gene IL-4v.C589T (rs2243250) (chromosome 5) (PCR-RFLP), we considered the relationships among particular genotypes with the possibility of occurrence of male infertility. Concentrations of chemical elements were measured in the blood. The activity of antioxidants and MDA levels were measured in serum. In the infertile group, higher GPx activity was noted (6.56 nmoL·min(−1)·mL(−1), control: 4.31 nmoL·min(−1)·mL(−1); p = 0.004), while GR achieved a greater level in the control (17.74 nmoL·min(−1)·mL(−1), infertile: 15.97 nmoL·min(−1)·mL(−1), p = 0.043), which implies diversified efficiency of the first and second lines of defense. The polymorphism of IL-4v.C589T (rs2243250) was not directly connected with infertility because there were not any differences in the frequency of genotypes between the infertile and control group (p = 0.578). An analysis of genotypes CC and TT (polymorphism IL-4v.C589T (rs2243250)) indicated numerous correlations between antioxidants, chemical elements and MDA. Therefore, chemical economy, antioxidative defense and genetic conditions are connected and jointly shape male reproductive potential. Chemical elements influence antioxidative defense and male fertility; the most important modulators appeared to be Na, Ba, Al and B. The polymorphism of gene IL-4v.C589T (rs2243250) has a limited influence on antioxidative defense and the metabolism of chemical elements. MDPI 2022-04-22 /pmc/articles/PMC9138092/ /pubmed/35624681 http://dx.doi.org/10.3390/antiox11050817 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Baszyński, Jędrzej
Kamiński, Piotr
Bogdzińska, Maria
Mroczkowski, Sławomir
Szymański, Marek
Wasilow, Karolina
Stanek, Emilia
Hołderna-Bona, Karolina
Brodzka, Sylwia
Bilski, Rafał
Tkachenko, Halyna
Kurhaluk, Natalia
Stuczyński, Tomasz
Lorek, Małgorzata
Woźniak, Alina
Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility
title Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility
title_full Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility
title_fullStr Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility
title_full_unstemmed Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility
title_short Enzymatic Antioxidant Defense and Polymorphic Changes in Male Infertility
title_sort enzymatic antioxidant defense and polymorphic changes in male infertility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138092/
https://www.ncbi.nlm.nih.gov/pubmed/35624681
http://dx.doi.org/10.3390/antiox11050817
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