Inhibition of proprotein convertase 5/6 activity: potential for nonhormonal women-centered contraception
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作者:
Aljofan, Mohamad
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Prince Henrys Inst Med Res, Clayton, Vic 3168, AustraliaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Aljofan, Mohamad
[1
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Singh, Harmeet
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Prince Henrys Inst Med Res, Clayton, Vic 3168, AustraliaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Singh, Harmeet
[1
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Ho, Huiting
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Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Monash Univ, Clayton, Vic 3169, AustraliaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Ho, Huiting
[1
,2
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Xie, Shuwu
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机构:
Shanghai Inst Planned Parenthood Res, NPFPC Key Lab Contracept & Devices, Shanghai 200032, Peoples R ChinaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Xie, Shuwu
[3
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Zhu, Yan
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Shanghai Inst Planned Parenthood Res, NPFPC Key Lab Contracept & Devices, Shanghai 200032, Peoples R ChinaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Zhu, Yan
[3
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Sun, Zhaogui
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Shanghai Inst Planned Parenthood Res, NPFPC Key Lab Contracept & Devices, Shanghai 200032, Peoples R ChinaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Sun, Zhaogui
[3
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Guo, Xiangjie
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Shanghai Inst Planned Parenthood Res, NPFPC Key Lab Contracept & Devices, Shanghai 200032, Peoples R ChinaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Guo, Xiangjie
[3
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Wang, Jian
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Monash Univ, Clayton, Vic 3169, AustraliaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Wang, Jian
[2
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Nie, Guiying
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Prince Henrys Inst Med Res, Clayton, Vic 3168, AustraliaPrince Henrys Inst Med Res, Clayton, Vic 3168, Australia
Nie, Guiying
[1
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机构:
[1] Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
[2] Monash Univ, Clayton, Vic 3169, Australia
[3] Shanghai Inst Planned Parenthood Res, NPFPC Key Lab Contracept & Devices, Shanghai 200032, Peoples R China
Background: Proprotein convertase 5/6 (PC6) is critical for endometrial epithelial receptivity and stromal cell decidualization for embryo implantation in women. We hypothesized that inhibiting PC6 could block implantation for contraception. The aim of this study was to prove this concept using human cell models and rabbits. Study Design: A potential PC6 inhibitor, C1239-PEG-Poly R, was biochemically confirmed to be a potent PC6 inhibitor. The potential contraceptive action of the inhibitor was then tested in decidualization of primary human endometrial stromal cells in a human trophoblast spheroid attachment model and in vivo in rabbits. Results: The PC6 inhibitor C1239-PEG-Poly R inhibited in a dose-dependent manner both decidualization and spheroid attachment. Vaginal delivery of 200 mu L of the inhibitor at a final concentration of 5 mM to rabbits over a 3-day period starting 6 days after mating resulted in a 60% decrease in implantation and, hence, pregnancy. Conclusions: This study presents proof of concept that PC6 inhibition has the potential to block embryo implantation, providing nonhormonal contraception for women. (C) 2012 Elsevier Inc. All rights reserved.