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短期母体地塞米松暴露后胎盘生长和 MAPK 的性别特异性变化在小鼠中。

Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse.

机构信息

School of Biomedical Sciences, The University of Queensland, St Lucia, 4072, Australia.

出版信息

Placenta. 2011 Dec;32(12):981-9. doi: 10.1016/j.placenta.2011.09.009. Epub 2011 Oct 5.

Abstract

OBJECTIVES

Maternal glucocorticoid (GC) exposure during pregnancy can alter fetal development and program the onset of disease in adult offspring. The placenta helps protect the fetus from excess GC exposure but is itself susceptible to maternal insults and may be involved in sex dependant regulation of fetal programming. This study aimed to investigate the effects of maternal GC exposure on the developing placenta.

STUDY DESIGN AND MAIN OUTCOME MEASURES

Pregnant mice were treated with dexamethasone (DEX-1 μg/kg/h) or saline (SAL) for 60 h via minipump beginning at E12.5. Placentas were collected at E14.5 and E17.5 and the expression of growth factors and placental transporters examined by real-time PCR and/or Western blot. Histological analysis was performed to assess for morphological changes.

RESULTS

At E14.5, DEX exposed male and female fetuses had a lower weight compared to SAL animals but placental weight was lower in females only. Hsd11b2 and Vegfa gene expression was increased and MAPK1 protein expression decreased in the placentas of females only. At E17.5 placental and fetal body weights were similar and differences in MAPK were no longer present although HSD11B2 protein was elevated in placentas of DEX females. Levels of glucose or amino acid transporters were unaffected.

CONCLUSIONS

Results suggest sex specific responses to maternal GCs within the placenta. Decreased levels of MAPK protein in placentas of female fetuses suggest alterations in the MAPK pathway may contribute to the lower placental weights in this sex. This may contribute towards sex specific fetal programming of adult disease.

摘要

目的

孕期母体糖皮质激素(GC)暴露可改变胎儿发育并启动成年后代疾病的发生。胎盘有助于保护胎儿免受GC 暴露的影响,但本身易受母体损伤的影响,并可能参与胎儿编程的性别依赖调节。本研究旨在探讨母体 GC 暴露对胎盘发育的影响。

研究设计和主要观察指标

通过迷你泵从 E12.5 开始,用地塞米松(DEX-1μg/kg/h)或生理盐水(SAL)处理怀孕小鼠 60 小时。在 E14.5 和 E17.5 收集胎盘,并通过实时 PCR 和/或 Western blot 检测生长因子和胎盘转运蛋白的表达。进行组织学分析以评估形态变化。

结果

在 E14.5,与 SAL 动物相比,DEX 暴露的雄性和雌性胎儿体重较低,但仅雌性胎盘重量较低。Hsd11b2 和 Vegfa 基因表达增加,MAPK1 蛋白表达仅在雌性胎盘减少。在 E17.5,胎盘和胎儿体重相似,MAPK 的差异不再存在,尽管 DEX 雌性胎盘中的 HSD11B2 蛋白升高。葡萄糖或氨基酸转运体水平不受影响。

结论

结果表明胎盘内母体 GC 存在性别特异性反应。雌性胎儿胎盘 MAPK 蛋白水平降低表明 MAPK 途径的改变可能导致该性别中胎盘重量降低。这可能有助于成年疾病的性别特异性胎儿编程。

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