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PMID: 23365651 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Vasopressin effectively suppresses male fertility.

PloS one ·Vol. 8 ·No. 1 ·2013-00-00 ·Pages e54192

Kwon WS, Park YJ, Kim YH, You YA, Kim IC, Pang MG

Abstract

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.

MeSH Terms
Acrosome/drug effects,metabolism Acrosome Reaction/drug effects Animals Arginine Vasopressin/pharmacology Calcium/metabolism Cyclic AMP-Dependent Protein Kinases/genetics,metabolism Deamino Arginine Vasopressin/pharmacology Embryo, Mammalian/physiology Embryonic Development/physiology Female Fertility/drug effects Fertilization in Vitro Hydrogen-Ion Concentration Male Mice Mice, Inbred ICR Phosphorylation/drug effects Receptors, Vasopressin/genetics,metabolism Sperm Capacitation/drug effects Sperm Count Sperm Motility/drug effects Tyrosine/metabolism
Chemicals
Receptors, Vasopressin Arginine Vasopressin Tyrosine Cyclic AMP-Dependent Protein Kinases Deamino Arginine Vasopressin Calcium
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kwon Woo-Sung
Department of Animal Science & Technology and BET Research Institute, School of Bioresource & Bioscience, Chung-Ang University, Anseong, Gyeonggi-do, Korea.
Park Yoo-Jin
Kim Yun-Hee
You Young-Ah
Kim In Cheul
Pang Myung-Geol
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2013-00-00
Epub
2013-00-24
Pages
e54192
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC3554711
Subset
IM
Corrections
CommentIn
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