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本文引用的文献

1
Non-genomic regulation of mammalian sperm hyperactivation.哺乳动物精子超激活的非基因组调控
Reprod Med Biol. 2009 Apr 23;8(2):47-52. doi: 10.1007/s12522-009-0012-2. eCollection 2009 Jun.
2
Regulation of hyperactivation of hamster spermatozoa by progesterone.孕酮对仓鼠精子超活化的调节。
Reprod Med Biol. 2008 Apr 17;7(2):63-74. doi: 10.1111/j.1447-0578.2008.00202.x. eCollection 2008 Jun.
3
Profiling of proteins phosphorylated or dephosphorylated during hyperactivation via activation on hamster spermatozoa.通过激活仓鼠精子超活化过程中磷酸化或去磷酸化蛋白质的分析。
Reprod Med Biol. 2006 May 19;5(2):123-135. doi: 10.1007/BF03016148. eCollection 2006 Jun.
4
Progesterone-enhanced sperm hyperactivation through IP-PKC and PKA signals.孕酮通过IP-PKC和PKA信号增强精子超激活。
Reprod Med Biol. 2012 Sep 12;12(1):27-33. doi: 10.1007/s12522-012-0137-6. eCollection 2013 Jan.
5
Serine/threonine phosphorylation associated with hamster sperm hyperactivation.与仓鼠精子超活化相关的丝氨酸/苏氨酸磷酸化
Reprod Med Biol. 2004 Dec 3;3(4):223-230. doi: 10.1111/j.1447-0578.2004.00069.x. eCollection 2004 Dec.
6
The clinical significance of calcium-signalling pathways mediating human sperm hyperactivation.介导人精子超激活的钙信号通路的临床意义。
Hum Reprod. 2013 Apr;28(4):866-76. doi: 10.1093/humrep/des467. Epub 2013 Feb 12.
7
Tubulin-dynein system in flagellar and ciliary movement.纤毛和鞭毛运动中的微管-动力蛋白系统。
Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(8):397-415. doi: 10.2183/pjab.88.397.
8
Behavioral mechanism during human sperm chemotaxis: involvement of hyperactivation.人类精子趋化性的行为机制:超激活作用的参与。
PLoS One. 2011;6(12):e28359. doi: 10.1371/journal.pone.0028359. Epub 2011 Dec 7.
9
Serotonin-enhanced hyperactivation of hamster sperm.提高血清素可增强仓鼠精子的超激活。
Reproduction. 2011 Aug;142(2):255-66. doi: 10.1530/REP-11-0074. Epub 2011 May 9.
10
Suppression of progesterone-enhanced hyperactivation in hamster spermatozoa by estrogen.雌激素抑制仓鼠精子中孕激素增强的超激活。
Reproduction. 2010 Sep;140(3):453-64. doi: 10.1530/REP-10-0168. Epub 2010 Jun 18.

孕酮、17β-雌二醇和己烯雌酚对仓鼠精子超激活的调节与干扰

Regulation and disruption of hamster sperm hyperactivation by progesterone, 17β-estradiol and diethylstilbestrol.

作者信息

Fujinoki Masakatsu

机构信息

Department of Physiology, School of Medicine Dokkyo Medical University 321-0293 Mibu Tochigi Japan.

出版信息

Reprod Med Biol. 2014 Jan 5;13(3):143-152. doi: 10.1007/s12522-013-0175-8. eCollection 2014 Jul.

DOI:10.1007/s12522-013-0175-8
PMID:29699158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5906959/
Abstract

PURPOSE

Hyperactivation of hamster sperm is dose-dependently enhanced by progesterone (P) and 17β-estradiol (E). In the first part of the present study, enhancement of hyperactivation in response to the concentrations of P and E was examined in detail and in the second part, it was examined whether enhancement of hyperactivation by P and E was disrupted by diethylstilbestrol (DES).

METHODS

Hamster spermatozoa were hyperactivated by incubation in modified Tyrode's albumin lactate pyruvate medium with P, E and/or DES. After spermatozoa were recorded using a video-microscope, observations were quantified by manually counting the numbers of total, motile and hyperactivated spermatozoa.

RESULTS

Hyperactivation was enhanced in response to the concentrations of P and E. When spermatozoa were exposed to DES with E, moreover, DES significantly and strongly suppressed P-enhanced hyperactivation by accelerating the effect of E, but DES itself only weakly suppressed P-enhanced hyperactivation.

CONCLUSIONS

Enhancement of hyperactivation was regulated by the concentrations of P and E, suggesting that in vivo hamster spermatozoa are hyperactivated through "monitoring" these concentrations in the oviduct. DES in combination with E suppressed P-enhanced hyperactivation, suggesting that DES significantly disrupts hyperactivation by acting as an accelerator of the effect of E.

摘要

目的

孕酮(P)和17β-雌二醇(E)可剂量依赖性地增强仓鼠精子的超活化。在本研究的第一部分,详细研究了P和E浓度对超活化增强的影响,在第二部分中,研究了己烯雌酚(DES)是否会破坏P和E对超活化的增强作用。

方法

将仓鼠精子在含有P、E和/或DES的改良Tyrode白蛋白乳酸丙酮酸培养基中孵育以使其超活化。使用视频显微镜记录精子后,通过手动计数总精子、活动精子和超活化精子的数量对观察结果进行量化。

结果

超活化随P和E的浓度增加而增强。此外,当精子与E一起暴露于DES时,DES通过加速E的作用显著且强烈地抑制了P增强的超活化,但DES本身仅微弱地抑制P增强的超活化。

结论

超活化的增强受P和E浓度的调节,这表明在体内仓鼠精子通过“监测”输卵管中的这些浓度而超活化。DES与E联合使用可抑制P增强的超活化,这表明DES通过作为E作用的促进剂而显著破坏超活化。