Vasopressin Effectively Suppresses Male Fertility

被引:45
|
作者
Kwon, Woo-Sung [1 ,2 ]
Park, Yoo-Jin [1 ,2 ]
Kim, Yun-Hee [1 ,2 ]
You, Young-Ah [1 ,2 ]
Kim, In Cheul [3 ]
Pang, Myung-Geol [1 ,2 ]
机构
[1] Chung Ang Univ, Sch Bioresource & Biosci, Dept Anim Sci & Technol, Anseong, Gyeonggi Do, South Korea
[2] Chung Ang Univ, Sch Bioresource & Biosci, BET Res Inst, Anseong, Gyeonggi Do, South Korea
[3] Rural Dev Adm, Natl Inst Anim Sci, Cheonan, Chungcheongnam, South Korea
来源
PLOS ONE | 2013年 / 8卷 / 01期
关键词
SPERM CAPACITATION; MOUSE SPERM; TYROSINE PHOSPHORYLATION; SPERMATOZOA; PROTEIN; IDENTIFICATION; OXYTOCIN; CALCIUM; FLUORESCENCE; EXPRESSION;
D O I
10.1371/journal.pone.0054192
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Ca2+ 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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页数:8
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