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Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation

17α-Estradiol (αE2) is a natural diastereoisomer of 17β-estradiol (E2). It is well known that αE2 can bind to estrogen receptors. However, its biological activity is less than that of E2 and is species and tissue specific. The goal of our study was to propose the mechanism of αE2 hormonal response i...

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Autores principales: Bosakova, Tereza, Tockstein, Antonin, Bosakova, Zuzana, Komrskova, Katerina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268409/
https://www.ncbi.nlm.nih.gov/pubmed/35807338
http://dx.doi.org/10.3390/molecules27134092
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author Bosakova, Tereza
Tockstein, Antonin
Bosakova, Zuzana
Komrskova, Katerina
author_facet Bosakova, Tereza
Tockstein, Antonin
Bosakova, Zuzana
Komrskova, Katerina
author_sort Bosakova, Tereza
collection PubMed
description 17α-Estradiol (αE2) is a natural diastereoisomer of 17β-estradiol (E2). It is well known that αE2 can bind to estrogen receptors. However, its biological activity is less than that of E2 and is species and tissue specific. The goal of our study was to propose the mechanism of αE2 hormonal response in rat sperm during their capacitation in vitro and compare it with a previously studied mouse model. Concentration changes in externally added αE2 during capacitation of rat sperm were monitored by the high-performance liquid chromatographic method with tandem mass spectrometric detection (HPLC-MS/MS). The calculated values of relative concentrations B(t) were subjected to kinetic analysis. The findings indicated that αE2 in rat sperm did not trigger autocatalytic reaction, in contrast to the mouse sperm, and that the initiation of the hormone penetration through the sperm plasma membrane was substantially faster in rats.
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spelling pubmed-92684092022-07-09 Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation Bosakova, Tereza Tockstein, Antonin Bosakova, Zuzana Komrskova, Katerina Molecules Article 17α-Estradiol (αE2) is a natural diastereoisomer of 17β-estradiol (E2). It is well known that αE2 can bind to estrogen receptors. However, its biological activity is less than that of E2 and is species and tissue specific. The goal of our study was to propose the mechanism of αE2 hormonal response in rat sperm during their capacitation in vitro and compare it with a previously studied mouse model. Concentration changes in externally added αE2 during capacitation of rat sperm were monitored by the high-performance liquid chromatographic method with tandem mass spectrometric detection (HPLC-MS/MS). The calculated values of relative concentrations B(t) were subjected to kinetic analysis. The findings indicated that αE2 in rat sperm did not trigger autocatalytic reaction, in contrast to the mouse sperm, and that the initiation of the hormone penetration through the sperm plasma membrane was substantially faster in rats. MDPI 2022-06-25 /pmc/articles/PMC9268409/ /pubmed/35807338 http://dx.doi.org/10.3390/molecules27134092 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
Bosakova, Tereza
Tockstein, Antonin
Bosakova, Zuzana
Komrskova, Katerina
Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation
title Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation
title_full Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation
title_fullStr Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation
title_full_unstemmed Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation
title_short Kinetic Study of 17α-Estradiol Mechanism during Rat Sperm Capacitation
title_sort kinetic study of 17α-estradiol mechanism during rat sperm capacitation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268409/
https://www.ncbi.nlm.nih.gov/pubmed/35807338
http://dx.doi.org/10.3390/molecules27134092
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