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血小板活化因子对小鼠胚胎体外着床的影响。

Effects of platelet activating factor on mouse embryo implantation in vitro.

作者信息

Nishi O, Tominaga T, Goto Y, Hayashi K, Mori T

机构信息

Department of Obstetrics and Gynecology, Fukui Medical School, Japan.

出版信息

J Assist Reprod Genet. 1995 May;12(5):330-4. doi: 10.1007/BF02213714.

Abstract

PURPOSE

Our purpose was to assess the role of platelet activating factor (PAF) in embryo implantation, we examined the effects of PAF and a PAF antagonist on the in vitro implantation of mouse embryos, using an in vitro embryo culture system in the absence of the endometrium.

METHODS

BDF1 mouse pronuclear-stage embryos were cultured until they developed to the two-cell, the four- to eight-cell, or the morula stage in the absence of PAF or its antagonist CV6209. The medium was then changed and supplemented with PAF or CV6209 at various concentrations. We also examined the reversible effects of PAF addition to the media containing the PAF antagonist.

RESULTS

The addition of PAF to the culture from the two-cell stage significantly (P < 0.05) increased the rates of embryo implantation in vitro (control, 69.8%; 10(-10) M PAF, 90.1%; 10(-9) M PAF, 95.5%). Similarly, the addition of PAF to the cultures from the four- to eight-cell and morula stage also significantly (P < 0.05) increased their rates of implantation in vitro. In contrast, the addition of CV6209 to the culture significantly (P < 0.01) decreased the rates of embryo implantation in vitro. CV6209 also decreased the rate of blastocyst formation. The degree of inhibition by CV6209 decreased with the advancing stage of embryos. The addition of PAF to media containing CV6209 reversed the inhibition and restored the implantation rate in vitro.

CONCLUSIONS

These results suggest that PAF may act directly on the mouse embryo and favor its implantation like an autocrine activating factor, irrespective of the presence or absence of the endometrium.

摘要

目的

我们的目的是评估血小板活化因子(PAF)在胚胎着床中的作用,我们使用无子宫内膜的体外胚胎培养系统,研究了PAF和一种PAF拮抗剂对小鼠胚胎体外着床的影响。

方法

将BDF1小鼠原核期胚胎在无PAF或其拮抗剂CV6209的情况下培养至二细胞、四至八细胞或桑椹胚阶段。然后更换培养基,并添加不同浓度的PAF或CV6209。我们还研究了向含有PAF拮抗剂的培养基中添加PAF的可逆作用。

结果

从二细胞期开始在培养中添加PAF显著(P<0.05)提高了体外胚胎着床率(对照组,69.8%;10^(-10)M PAF,90.1%;10^(-9)M PAF,95.5%)。同样,从四至八细胞期和桑椹胚期开始在培养中添加PAF也显著(P<0.05)提高了它们的体外着床率。相反,在培养中添加CV6209显著(P<0.01)降低了体外胚胎着床率。CV6209也降低了囊胚形成率。CV6209的抑制程度随着胚胎发育阶段的推进而降低。向含有CV6209的培养基中添加PAF可逆转抑制作用并恢复体外着床率。

结论

这些结果表明,PAF可能直接作用于小鼠胚胎,像自分泌激活因子一样有利于其着床,而与子宫内膜的有无无关。

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