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雄激素对小鼠延迟着床模型中胚胎着床的影响。

Effects of androgen on embryo implantation in the mouse delayed-implantation model.

作者信息

Diao Hong-Lu, Su Ren-Wei, Tan Hui-Ning, Li Shi-Jie, Lei Wei, Deng Weng-Bo, Yang Zeng-Ming

机构信息

College of Life Science, Xiamen University, Xiamen, China.

出版信息

Fertil Steril. 2008 Oct;90(4 Suppl):1376-83. doi: 10.1016/j.fertnstert.2007.07.1341. Epub 2007 Dec 3.

Abstract

OBJECTIVE

To examine the effects of androgen on implantation and decidualization in the mouse delayed-implantation model.

DESIGN

Experimental animal study.

SETTING

University research laboratory.

ANIMAL(S): Sexually mature female mice (Kunming White strain).

INTERVENTION(S): Delayed and activated implantation; pseudopregnancy; embryo transfer (ET); E(2) assay; inhibitor.

MAIN OUTCOME MEASURE(S): Effects of androgen on embryo implantation were determined by treating the mice under delayed implantation with different doses of testosterone propionate (TP); the effects of androgen on the expression of implantation-related genes were examined by in situ hybridization.

RESULT(S): Delayed implantation could be initiated by TP. Dihydrotestosterone was also able to initiate implantation in the delayed-implantation model. The implantation window could be maintained for at least 48 hours by 5 mg TP per mouse. Prostaglandin endoperoxide synthase 2 (Ptgs2) and microsomal prostaglandin E synthase (mPtges) were aberrantly expressed in mouse uterus at implantation sites after delayed implantation was activated by high doses of TP.

CONCLUSION(S): A low dose of TP led to a delay in embryo implantation, but a high dose caused aberrant expression of both Ptgs2 and mPtges at the implantation site. It is possible that high doses of TP may disturb peri-implantation development or may be involved in early pregnancy loss by disturbing the uterine prostaglandin system.

摘要

目的

在小鼠延迟着床模型中研究雄激素对着床和蜕膜化的影响。

设计

实验动物研究。

地点

大学研究实验室。

动物

性成熟雌性小鼠(昆明品系)。

干预措施

延迟和激活着床;假孕;胚胎移植(ET);雌二醇(E₂)检测;抑制剂。

主要观察指标

通过用不同剂量丙酸睾酮(TP)处理处于延迟着床状态的小鼠来确定雄激素对胚胎着床的影响;通过原位杂交检测雄激素对着床相关基因表达的影响。

结果

TP可启动延迟着床。双氢睾酮也能够在延迟着床模型中启动着床。每只小鼠给予5mg TP可使着床窗口维持至少48小时。高剂量TP激活延迟着床后,前列腺素内过氧化物合酶2(Ptgs2)和微粒体前列腺素E合酶(mPtges)在小鼠子宫着床部位异常表达。

结论

低剂量TP导致胚胎着床延迟,但高剂量会使着床部位的Ptgs2和mPtges均异常表达。高剂量TP可能通过干扰子宫前列腺素系统扰乱着床周围发育或导致早期妊娠丢失。

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