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Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress
Hydrogen sulphide (H(2)S) is involved in the physiology and pathophysiology of different cell types, but little is known about its role in sperm cells. Because of its reducing properties, we hypothesise that H(2)S protects spermatozoa against the deleterious effects of oxidative stress, a condition...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162918/ https://www.ncbi.nlm.nih.gov/pubmed/32300246 http://dx.doi.org/10.1038/s41598-020-63489-4 |
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author | Pintus, Eliana Jovičić, Marija Kadlec, Martin Ros-Santaella, José Luis |
author_facet | Pintus, Eliana Jovičić, Marija Kadlec, Martin Ros-Santaella, José Luis |
author_sort | Pintus, Eliana |
collection | PubMed |
description | Hydrogen sulphide (H(2)S) is involved in the physiology and pathophysiology of different cell types, but little is known about its role in sperm cells. Because of its reducing properties, we hypothesise that H(2)S protects spermatozoa against the deleterious effects of oxidative stress, a condition that is common to several male fertility disorders. This study aimed i) to determine the total antioxidant capacities of Na(2)S and GYY4137, which are fast- and slow-releasing H(2)S donors, respectively, and ii) to test whether H(2)S donors are able to protect spermatozoa against oxidative stress. We found that Na(2)S and GYY4137 show different antioxidant properties, with the total antioxidant capacity of Na(2)S being mostly unstable and even undetectable at 150 µM. Moreover, both H(2)S donors preserve sperm motility and reduce acrosome loss, although the effects were both dose and donor dependent. Within the range of concentrations tested (3–300 µM), GYY4137 showed positive effects on sperm motility, whereas Na(2)S was beneficial at the lowest concentration but detrimental at the highest. Our findings show that Na(2)S and GYY4137 have different antioxidant properties and suggest that both H(2)S donors might be used as in vitro therapeutic agents against oxidative stress in sperm cells, although the optimal therapeutic range differs between the compounds. |
format | Online Article Text |
id | pubmed-7162918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71629182020-04-23 Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress Pintus, Eliana Jovičić, Marija Kadlec, Martin Ros-Santaella, José Luis Sci Rep Article Hydrogen sulphide (H(2)S) is involved in the physiology and pathophysiology of different cell types, but little is known about its role in sperm cells. Because of its reducing properties, we hypothesise that H(2)S protects spermatozoa against the deleterious effects of oxidative stress, a condition that is common to several male fertility disorders. This study aimed i) to determine the total antioxidant capacities of Na(2)S and GYY4137, which are fast- and slow-releasing H(2)S donors, respectively, and ii) to test whether H(2)S donors are able to protect spermatozoa against oxidative stress. We found that Na(2)S and GYY4137 show different antioxidant properties, with the total antioxidant capacity of Na(2)S being mostly unstable and even undetectable at 150 µM. Moreover, both H(2)S donors preserve sperm motility and reduce acrosome loss, although the effects were both dose and donor dependent. Within the range of concentrations tested (3–300 µM), GYY4137 showed positive effects on sperm motility, whereas Na(2)S was beneficial at the lowest concentration but detrimental at the highest. Our findings show that Na(2)S and GYY4137 have different antioxidant properties and suggest that both H(2)S donors might be used as in vitro therapeutic agents against oxidative stress in sperm cells, although the optimal therapeutic range differs between the compounds. Nature Publishing Group UK 2020-04-16 /pmc/articles/PMC7162918/ /pubmed/32300246 http://dx.doi.org/10.1038/s41598-020-63489-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Pintus, Eliana Jovičić, Marija Kadlec, Martin Ros-Santaella, José Luis Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress |
title | Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress |
title_full | Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress |
title_fullStr | Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress |
title_full_unstemmed | Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress |
title_short | Divergent effect of fast- and slow-releasing H(2)S donors on boar spermatozoa under oxidative stress |
title_sort | divergent effect of fast- and slow-releasing h(2)s donors on boar spermatozoa under oxidative stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162918/ https://www.ncbi.nlm.nih.gov/pubmed/32300246 http://dx.doi.org/10.1038/s41598-020-63489-4 |
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