Ultrasound in Medicine and Biology
Volume 34, Issue 5 , Pages 741-752, May 2008

Cardiovascular Assessment of Fetal Mice by In Utero Echocardiography

  • Qing Yu

      Affiliations

    • Laboratory of Developmental Biology, National Heart Lung and Blood Institute, Bethesda, Maryland, USA
  • ,
  • Linda Leatherbury

      Affiliations

    • Laboratory of Developmental Biology, National Heart Lung and Blood Institute, Bethesda, Maryland, USA
    • Children's National Heart Institute, Children's National Medical Center; Washington, D.C., USA
  • ,
  • Xin Tian

      Affiliations

    • Office of Biostatistics Research; National Heart Lung and Blood Institute, Bethesda, Maryland, USA
  • ,
  • C.W. Lo

      Affiliations

    • Laboratory of Developmental Biology, National Heart Lung and Blood Institute, Bethesda, Maryland, USA
    • Corresponding Author InformationAddress correspondence to: Dr. Cecilia Lo, 9000 Rockville Pike, NIH/NHLBI/LDB, Building 10/Room 6C103A, Bethesda, MD 20814 USA.

Received 23 January 2007; received in revised form 27 September 2007; accepted 1 November 2007. published online 07 March 2008.

Abstract 

To establish a developmental profile of fetal mouse cardiovascular parameters, we analyzed a large body of ultrasound measurements obtained by in utero echocardiography of C57BL/6J fetal mice from embryonic day 12.5 to 19.5 (term). Measurements were obtained using two-dimensional (2D), spectral Doppler and M-mode imaging with standard clinical cardiac ultrasound imaging planes. As these studies were conducted as part of a large scale mouse mutagenesis screen, stringent filtering criteria were used to eliminate potentially abnormal fetuses. Our analysis showed heart rate increased from 190 to 245 beats per minute as the mouse fetus grew from 8 mm at embryonic day 12.5 to 18.7 mm at term. This was accompanied by increases in peak outflow velocity, E-wave, E/A ratio and ventricular dimensions. In contrast, the A-wave, myocardial performance index and isovolemic contraction time decreased gradually. Systolic function remained remarkably stable at 80% ejection fraction. Analysis of intra- and interobserver variabilities showed these parameters were reproducible, with most comparing favorably to clinical ultrasound measurements in human fetuses. A comprehensive database was generated comprising 23 echocardiographic parameters delineating fetal mouse cardiovascular function from embryonic day 12.5 to term. This database can serve as a standard for evaluating cardiovascular pathophysiology in genetically altered and mutant mouse models. (E-mail: loc@nhlbi.nih.gov)

Key Words: Fetal ultrasound, Image comparison, Mouse fetus, Development, Cardiovascular system

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PII: S0301-5629(07)00561-3

doi:10.1016/j.ultrasmedbio.2007.11.001

Ultrasound in Medicine and Biology
Volume 34, Issue 5 , Pages 741-752, May 2008