小鼠妊娠期羊水的体积和组成。

Cecilia Y Cheung, Robert A Brace
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引用次数: 33

摘要

目的:本研究旨在确定妊娠小鼠羊水(AF)体积和成分在妊娠期间的同步变化。方法:对CB6F1株幼鼠(6 ~ 7周龄)进行夜间交配。从胚胎第9.5 ~ 18.5天连续采集AF,测定其体积和组成。统计分析包括单因素方差分析(ANOVA)。结果:AF体积从9.5天的18 +/- 4 (SE) microL增加到15.5 ~ 16.5天的147 +/- 4 microL,在18.5天急剧下降到17 +/- 3 microL。房颤渗透压在分娩前19.5至20.5天没有变化。房颤钠、钙和葡萄糖浓度随妊娠进展先升高后降低。房颤钾、氯和乳酸浓度在整个妊娠期先降低后升高。在第9.5天之前和第18.5天之后,AF体积太小,无法进行体积或成分测定。结论:在小鼠中,心房纤颤体积从妊娠中期到妊娠后期最大的上升与人类相似,而在分娩前急剧下降与人类不同。正如在胎羊中观察到的那样,液体体积的变化与心房纤溶压和溶质浓度的变化有关,这些变化与胎龄的增加有关。这些观察结果以及在小鼠胎儿中量化心房颤动体积和组成的可行性表明,利用转基因小鼠作为未来研究心房颤动体积和组成调控的分子机制的模型是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amniotic fluid volume and composition in mouse pregnancy.

Objective: The current study was undertaken to determine simultaneous changes in amniotic fluid (AF) volume and composition across gestation in the pregnant mouse.

Methods: Young adult mice (6 to 7 weeks old) of the CB6F1 strain were mated overnight. AF was collected on consecutive days from embryonic days 9.5 through 18.5 for measurements of volume and composition. Statistical analysis included one-factor analysis of variance (ANOVA).

Results: AF volume increased from 18 +/- 4 (SE) microL on day 9.5 to a maximum of 147 +/- 4 microL on days 15.5 to 16.5 and decreased sharply to 17 +/- 3 microL on day 18.5. AF osmolality was unchanged except for a rise prior to delivery on day 19.5 to 20.5. AF sodium, calcium, and glucose concentrations increased and subsequently decreased as gestation progressed. AF potassium, chloride, and lactate concentrations initially decreased and then increased across gestation. Prior to day 9.5 and after day 18.5, AF volume was too small for volume or compositional determinations.

Conclusions: In the mouse, the rise in AF volume from mid gestation to a maximum late in gestation is similar to that in humans while the sharp fall prior to delivery is not. As observed in the fetal sheep, the changes in fluid volume are associated with AF osmolality and solute concentration changes that are correlated with advancing gestational age. These observations together with the feasibility of quantifying AF volume and composition in the mouse fetus demonstrate the possibility of using genetically altered mice as a model for future studies on the molecular mechanisms underlying the regulation of AF volume and composition.

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