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Vasopressin Effectively Suppresses Male Fertility

Arginine vasopressin (VP) is neurohypophysial hormone has been implicated in stimulating contractile activity of the male reproductive tract in the testis. Higher levels of VP decrease sperm count and motility. However, very little is known about the involvement of VP in controlling mammalian reprod...

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Autores principales: Kwon, Woo-Sung, Park, Yoo-Jin, Kim, Yun-Hee, You, Young-Ah, Kim, In Cheul, Pang, Myung-Geol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554711/
https://www.ncbi.nlm.nih.gov/pubmed/23365651
http://dx.doi.org/10.1371/journal.pone.0054192
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author Kwon, Woo-Sung
Park, Yoo-Jin
Kim, Yun-Hee
You, Young-Ah
Kim, In Cheul
Pang, Myung-Geol
author_facet Kwon, Woo-Sung
Park, Yoo-Jin
Kim, Yun-Hee
You, Young-Ah
Kim, In Cheul
Pang, Myung-Geol
author_sort Kwon, Woo-Sung
collection PubMed
description Arginine vasopressin (VP) is neurohypophysial hormone has been implicated in stimulating contractile activity of the male reproductive tract in the testis. Higher levels of VP decrease sperm count and motility. However, very little is known about the involvement of VP in controlling mammalian reproductive process. The goal of this study was to confirm that effect of VP receptor (AVPR2) on sperm function in capacitation condition. Deamino [Cys 1, D-ArgS] vasopressin (dDAVP), an AVPR2 agonist that operates only on AVPR2, was used. Also, Mouse spermatozoa were incubated with various concentrations of dDAVP (10(−11)–10(−5) M) and sperm motility, capacitation status, Protein Kinase A activity (PKA), tyrosine phosphorylation, fertilization, and embryo development were assessed using computer-assisted sperm analysis, Combined Hoechst 33258/chlortetracycline fluorescence, Western blotting, and in vitro fertilization, respectively. AVPR2 was placed on the acrosome region and mid-piece in cauda epididymal spermatozoa, but the caput epididymal spermatozoa was mid-piece only. The high dDAVP treatment (10(−8) and 10(−5) M) significantly decreased sperm motility, intracellular pH and PKA substrates (approximately 55 and 22 kDa) and increased Ca(2+) concentration. The highest concentration treatment significantly decreased PKA substrate (approximately 23 kDa) and tyrosine phosphorylation (approximately 30 kDa). VP detrimentally affected capacitation, acrosome reaction, and embryo development. Treatment with the lowest concentration (10(−11) M) was not significantly different. Our data have shown that VP stimulates ion transport across sperm membrane through interactions with AVPR2. VP has a detrimental effect in sperm function, fertilization, and embryonic development, suggesting its critical role in the acquisition of fertilizing ability of mouse spermatozoa. These research findings will enable further study to determine molecular mechanism associated with fertility in capacitation and fertilization. It is also an important pivotal precondition to the progress of diagnostic test to identify infertility and to apply male contraception.
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spelling pubmed-35547112013-01-30 Vasopressin Effectively Suppresses Male Fertility Kwon, Woo-Sung Park, Yoo-Jin Kim, Yun-Hee You, Young-Ah Kim, In Cheul Pang, Myung-Geol PLoS One Research Article Arginine vasopressin (VP) is neurohypophysial hormone has been implicated in stimulating contractile activity of the male reproductive tract in the testis. Higher levels of VP decrease sperm count and motility. However, very little is known about the involvement of VP in controlling mammalian reproductive process. The goal of this study was to confirm that effect of VP receptor (AVPR2) on sperm function in capacitation condition. Deamino [Cys 1, D-ArgS] vasopressin (dDAVP), an AVPR2 agonist that operates only on AVPR2, was used. Also, Mouse spermatozoa were incubated with various concentrations of dDAVP (10(−11)–10(−5) M) and sperm motility, capacitation status, Protein Kinase A activity (PKA), tyrosine phosphorylation, fertilization, and embryo development were assessed using computer-assisted sperm analysis, Combined Hoechst 33258/chlortetracycline fluorescence, Western blotting, and in vitro fertilization, respectively. AVPR2 was placed on the acrosome region and mid-piece in cauda epididymal spermatozoa, but the caput epididymal spermatozoa was mid-piece only. The high dDAVP treatment (10(−8) and 10(−5) M) significantly decreased sperm motility, intracellular pH and PKA substrates (approximately 55 and 22 kDa) and increased Ca(2+) concentration. The highest concentration treatment significantly decreased PKA substrate (approximately 23 kDa) and tyrosine phosphorylation (approximately 30 kDa). VP detrimentally affected capacitation, acrosome reaction, and embryo development. Treatment with the lowest concentration (10(−11) M) was not significantly different. Our data have shown that VP stimulates ion transport across sperm membrane through interactions with AVPR2. VP has a detrimental effect in sperm function, fertilization, and embryonic development, suggesting its critical role in the acquisition of fertilizing ability of mouse spermatozoa. These research findings will enable further study to determine molecular mechanism associated with fertility in capacitation and fertilization. It is also an important pivotal precondition to the progress of diagnostic test to identify infertility and to apply male contraception. Public Library of Science 2013-01-24 /pmc/articles/PMC3554711/ /pubmed/23365651 http://dx.doi.org/10.1371/journal.pone.0054192 Text en © 2013 Kwon et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kwon, Woo-Sung
Park, Yoo-Jin
Kim, Yun-Hee
You, Young-Ah
Kim, In Cheul
Pang, Myung-Geol
Vasopressin Effectively Suppresses Male Fertility
title Vasopressin Effectively Suppresses Male Fertility
title_full Vasopressin Effectively Suppresses Male Fertility
title_fullStr Vasopressin Effectively Suppresses Male Fertility
title_full_unstemmed Vasopressin Effectively Suppresses Male Fertility
title_short Vasopressin Effectively Suppresses Male Fertility
title_sort vasopressin effectively suppresses male fertility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554711/
https://www.ncbi.nlm.nih.gov/pubmed/23365651
http://dx.doi.org/10.1371/journal.pone.0054192
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