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经阴道给予聚乙二醇化 LIF 拮抗剂可阻止胚胎着床,并消除对小鼠骨骼的非靶标作用。

Vaginally administered PEGylated LIF antagonist blocked embryo implantation and eliminated non-target effects on bone in mice.

机构信息

Embryo Implantation, Prince Henry's Institute, Clayton, Australia.

出版信息

PLoS One. 2011;6(5):e19665. doi: 10.1371/journal.pone.0019665. Epub 2011 May 18.

Abstract

Female-controlled contraception/HIV prevention is critical to address health issues associated with gender inequality. Therefore, a contraceptive which can be administered in tandem with a microbicide to inhibit sexually transmitted infections, is desirable. Uterine leukemia inhibitory factor (LIF) is obligatory for blastocyst implantation in mice and associated with infertility in women. We aimed to determine whether a PEGylated LIF inhibitor (PEGLA) was an effective contraceptive following vaginal delivery and to identify non-uterine targets of PEGLA in mice.Vaginally-applied (125)I-PEGLA accumulated in blood more slowly (30 min vs 10 min) and showed reduced tissue and blood retention (24 h vs 96 h) compared to intraperitoneal injection in mice. Vaginally-applied PEGLA blocked implantation. PEGLA administered by intraperitoneal injection inhibited bone remodelling whereas vaginally-applied PEGLA had no effect on bone. Further, PEGLA had no effect in an animal model of multiple sclerosis, experimental auto-immune encephalomyelitis, suggesting PEGLA cannot target the central nervous system.Vaginally-administered PEGLA is a promising non-hormonal contraceptive, one which could be delivered alone, or in tandem with a microbicide. Vaginal application reduced the total dose of PEGLA required to block implantation and eliminated the systemic effect on bone, showing the vagina is a promising site of administration for larger drugs which target organs within the reproductive tract.

摘要

女性控制的避孕/艾滋病毒预防对于解决与性别不平等相关的健康问题至关重要。因此,需要一种可以与杀微生物剂联合使用以抑制性传播感染的避孕方法。子宫白血病抑制因子(LIF)对于小鼠的胚泡着床是必需的,并且与女性的不孕有关。我们旨在确定阴道分娩后聚乙二醇化 LIF 抑制剂(PEGLA)是否是一种有效的避孕方法,并确定 PEGLA 在小鼠中的非子宫靶标。阴道应用(125)I-PEGLA 在血液中的积累速度较慢(30 分钟比 10 分钟),并且与腹腔注射相比,组织和血液保留时间减少(24 小时比 96 小时)。阴道应用 PEGLA 可阻止着床。腹腔内注射 PEGLA 可抑制骨重塑,而阴道应用 PEGLA 对骨无影响。此外,PEGLA 在多发性硬化症、实验性自身免疫性脑脊髓炎的动物模型中没有作用,这表明 PEGLA 不能靶向中枢神经系统。阴道给药的 PEGLA 是一种有前途的非激素避孕药,可单独使用,也可与杀微生物剂联合使用。阴道给药可减少阻止着床所需的 PEGLA 总剂量,并消除对骨骼的全身影响,这表明阴道是一种有前途的给药部位,可以为靶向生殖道内器官的较大药物提供给药途径。

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