Aristizábal O, Christopher D A, Foster F S, Turnbull D H
Skirball Institute of Biomolecular Medicine, New York University Medical Center, NY 10016, USA.
Ultrasound Med Biol. 1998 Nov;24(9):1407-17. doi: 10.1016/s0301-5629(98)00132-x.
Congenital heart disease results from genetic defects that are manifested at early stages of embryogenesis. The mouse is the preferred animal model for studies of mammalian embryonic development and for an increasing number of human disease models. A number of genes identified in the mouse are critical for normal cardiovascular development, but an understanding of the underlying mechanisms regulating heart development is still incomplete, in part because of the lack of methods to measure hemodynamics in live mouse embryos. We describe the development of a 40-MHz ultrasound scanner, which allows image-guided continuous-wave and pulsed Doppler blood flow measurements in mouse embryos, in utero, at the critical early developmental stages. Doppler waveforms acquired from mouse embryonic umbilical vessels, descending aorta, and cardiac ventricles are presented to demonstrate the utility of the method. By combining image-guided ultrasound Doppler with the many available mouse mutants, this approach should lead to new insights into embryonic cardiovascular structure-function relationships.
先天性心脏病由在胚胎发育早期阶段显现的基因缺陷导致。小鼠是用于研究哺乳动物胚胎发育以及越来越多人类疾病模型的首选动物模型。在小鼠中鉴定出的许多基因对正常心血管发育至关重要,但对调节心脏发育的潜在机制的理解仍不完整,部分原因是缺乏在活体小鼠胚胎中测量血流动力学的方法。我们描述了一种40兆赫超声扫描仪的开发,该扫描仪能够在子宫内关键的早期发育阶段对小鼠胚胎进行图像引导下的连续波和脉冲多普勒血流测量。展示了从小鼠胚胎脐血管、降主动脉和心室获取的多普勒波形,以证明该方法的实用性。通过将图像引导超声多普勒与许多现有的小鼠突变体相结合,这种方法应该会为胚胎心血管结构 - 功能关系带来新的见解。