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Ultrasound diagnosis of mouse pregnancy and gestational staging

机译:小鼠妊娠和妊娠分期的超声诊断

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Phenotypic analysis of mutant mice is limited by lack of accurate, simple, and nondestructive in utero imaging techniques. This study evaluated the usefulness of ultrasound imaging (US) to stage fetal mouse gestational age (GA) and depict morphologic development. We imaged 16 pregnant CD-1 mice and a total of 92 fetuses with a 15-MHz US transducer from 9.5 d postcoitus (DPC) until 20.5 DPC or delivery. Parameters recorded included gestational sac dimensions, crown-rump length (CRL), biparietal diameter (BPD), thoracoabdominal diameter (TAD), onset of cardiac activity, and morphologic development. At 9.5 d DPC, all gestations appeared as rounded sacs, with a diameter (mean +/- standard error) of 4.4 +/- 1 mm. BPD, CRL, and GA were highly correlated. The following structures were first identifiable at the following GA: cardiac activity, 10.5 DPC; major cardiovascular structures, 11.5 DPC; limb buds, 10.5 DPC; spine, 12.5 DPC; face and skull ossification, 13.5 DPC; rib ossification, 15.5 DPC; hind- and forelimb digits, 15.5 DPC; stomach and urinary bladder, 17.5 DPC; visualization of the rhombencephalic vesicle, 13.5 DPC; and visualization of the lateral ventricles, 14.5 DPC. The echogenic lungs were distinct from the liver as early as 12.5 DPC. The circle of Willis was detectable with color Doppler as early as 13.5 DPC and was easily visualized at 15.5 DPC. We found that US provides accurate, simple staging criteria for fetal mouse gestational development after 9.5 DPC and may be a nondestructive means of documenting phenotypic alterations in mutant mice in utero.
机译:突变小鼠的表型分析受到子宫成像技术缺乏准确,简单和无损的限制。这项研究评估了超声成像(US)对胎儿小鼠胎龄(GA)进行分期并描述形态发育的有用性。我们对16个怀孕的CD-1小鼠和92个胎儿进行了成像,这些胎儿从9.5 d后性交(DPC)直到20.5 DPC或分娩都使用了15 MHz的US换能器。记录的参数包括胎囊尺寸,冠臀长(CRL),双顶径(BPD),胸腹径(TAD),心脏活动发作和形态发育。在9.5 d DPC时,所有妊娠均显示为圆形囊,直径(平均+/-标准误差)为4.4 +/- 1毫米。 BPD,CRL和GA高度相关。在以下GA中首先可以识别以下结构:心脏活动,10.5 DPC;主要心血管结构,11.5 DPC;肢芽,10.5 DPC;脊柱,12.5 DPC;面部和颅骨骨化,13.5 DPC;肋骨骨化,15.5 DPC;后肢和前肢数字,15.5 DPC;胃和膀胱,17.5 DPC;可视化菱形脑小泡,13.5 DPC;和侧脑室的可视化14.5 DPC。回声肺早在12.5 DPC时就与肝脏截然不同。彩色多普勒最早可检测到Willis圆,在13.5 DPC时很容易看到。我们发现,US为9.5 DPC后胎儿小鼠的妊娠发育提供了准确,简单的分期标准,并且可能是记录子宫内突变小鼠表型改变的一种非破坏性手段。

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