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Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential

BACKGROUND: Infertility is an important worldwide problem which affects 10–15% of couples globally. Altered NO production has also been implicated in the pathogenesis of the male infertility. The present study was designed to evaluate the changes in the activity of NO-synthase (NOS) and arginase in...

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Autores principales: Fafula, Roman V., Iefremova, Ulyana P., Onufrovych, Olena K., Maksymyuk, Hanna V., Besedina, Anna S., Nakonechnyi, Iosyf A., Vorobets, Dmytro Z., Vorobets, Zinoviy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294095/
https://www.ncbi.nlm.nih.gov/pubmed/30581349
http://dx.doi.org/10.1515/jomb-2017-0049
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author Fafula, Roman V.
Iefremova, Ulyana P.
Onufrovych, Olena K.
Maksymyuk, Hanna V.
Besedina, Anna S.
Nakonechnyi, Iosyf A.
Vorobets, Dmytro Z.
Vorobets, Zinoviy D.
author_facet Fafula, Roman V.
Iefremova, Ulyana P.
Onufrovych, Olena K.
Maksymyuk, Hanna V.
Besedina, Anna S.
Nakonechnyi, Iosyf A.
Vorobets, Dmytro Z.
Vorobets, Zinoviy D.
author_sort Fafula, Roman V.
collection PubMed
description BACKGROUND: Infertility is an important worldwide problem which affects 10–15% of couples globally. Altered NO production has also been implicated in the pathogenesis of the male infertility. The present study was designed to evaluate the changes in the activity of NO-synthase (NOS) and arginase in spermatozoa of patients with infertility. METHODS: The total NOS, Ca(2+)-dependent constitutive (cNOS) and Ca(2+)-independent inducible (iNOS) activity and arginase activity were assessed in sperm cells of patients with different forms of pathospermia. RESULTS: We found a significant increase in iNOS activity, but significantly decreased cNOS and arginase activity in sperm cells of infertile men vs fertile, normozoospermic men (p<0.001). The arginase/NOS ratio significantly decreased compared to control group. The iNOS/cNOS ratio was drastically increased in patients with decreased fertility potential indicating predominance of iNOS. Men with leuko cytospermia were distinguished to have the most express iNOS activity. CONCLUSIONS: These observations provide evidence for a disturbed balance between the L-arginine metabolic pathways in sperm cells of infertile men. This imbalance includes the considerable activation of the inducible isoform of NO-synthase accompanied by significant inhibition of its constitutive isoform which indicates disturbances in NO production. In patients with decreased fertility potential the arginase/NOS was shifted towards predominance of iNOS-derived NO production.
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spelling pubmed-62940952018-12-21 Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential Fafula, Roman V. Iefremova, Ulyana P. Onufrovych, Olena K. Maksymyuk, Hanna V. Besedina, Anna S. Nakonechnyi, Iosyf A. Vorobets, Dmytro Z. Vorobets, Zinoviy D. J Med Biochem Original Paper BACKGROUND: Infertility is an important worldwide problem which affects 10–15% of couples globally. Altered NO production has also been implicated in the pathogenesis of the male infertility. The present study was designed to evaluate the changes in the activity of NO-synthase (NOS) and arginase in spermatozoa of patients with infertility. METHODS: The total NOS, Ca(2+)-dependent constitutive (cNOS) and Ca(2+)-independent inducible (iNOS) activity and arginase activity were assessed in sperm cells of patients with different forms of pathospermia. RESULTS: We found a significant increase in iNOS activity, but significantly decreased cNOS and arginase activity in sperm cells of infertile men vs fertile, normozoospermic men (p<0.001). The arginase/NOS ratio significantly decreased compared to control group. The iNOS/cNOS ratio was drastically increased in patients with decreased fertility potential indicating predominance of iNOS. Men with leuko cytospermia were distinguished to have the most express iNOS activity. CONCLUSIONS: These observations provide evidence for a disturbed balance between the L-arginine metabolic pathways in sperm cells of infertile men. This imbalance includes the considerable activation of the inducible isoform of NO-synthase accompanied by significant inhibition of its constitutive isoform which indicates disturbances in NO production. In patients with decreased fertility potential the arginase/NOS was shifted towards predominance of iNOS-derived NO production. Sciendo 2018-04-01 /pmc/articles/PMC6294095/ /pubmed/30581349 http://dx.doi.org/10.1515/jomb-2017-0049 Text en © 2018 Roman V. Fafula, Ulyana P. Iefremova, Olena K. Onufrovych, Hanna V. Maksymyuk, Anna S. Besedina, Iosyf A. Nakonechnyi, Dmytro Z. Vorobets, Zinoviy D. Vorobets published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Original Paper
Fafula, Roman V.
Iefremova, Ulyana P.
Onufrovych, Olena K.
Maksymyuk, Hanna V.
Besedina, Anna S.
Nakonechnyi, Iosyf A.
Vorobets, Dmytro Z.
Vorobets, Zinoviy D.
Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential
title Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential
title_full Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential
title_fullStr Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential
title_full_unstemmed Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential
title_short Alterations in Arginase-NO-synthase System of Spermatozoa in Human Subjects with Different Fertility Potential
title_sort alterations in arginase-no-synthase system of spermatozoa in human subjects with different fertility potential
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294095/
https://www.ncbi.nlm.nih.gov/pubmed/30581349
http://dx.doi.org/10.1515/jomb-2017-0049
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