N. Tanaka et al., LEFT-VENTRICULAR VOLUMES AND FUNCTION IN THE EMBRYONIC MOUSE HEART, American journal of physiology. Heart and circulatory physiology, 42(3), 1997, pp. 1368-1376
This study describes miniaturized technology for the in vivo analysis
of the volume and function of the embryonic mouse heart and the applic
ation of this technology to study the normal embryonic left ventricle
(LV) at two stages of development. With the use of microsurgical techn
iques, embryos from embryonic clay (ED) 10.5 (ED10.5) to ED16 were del
ivered individually from litters of normal dams, and cardiac visualiza
tion was achieved with the use of intravital microscopy by transillumi
nation, with the umbilical circulation intact. At ED10.5-11, the heart
could be imaged in color in the intact embryo, whereas at ED12.5 it w
as necessary to open the chest; at ED13.5-14.5, fluorescent imaging wi
th the use of microinjection of fluorescein-conjugated albumin was nec
essary to visualize the LV chamber. At ED10.5-11, the LV end-diastolic
volumes averaged 0.16 mu l (n = 14), and at ED13.5-14.5, they average
d 0.57 mu l (n = 16). At both ages there was a positive linear relatio
nship between the LV end-diastolic volume and the stroke volume despit
e substantial variations in individual heart rates, reflecting the rel
ative uniformity of the LV ejection fractions within each age group. T
he average of the individual ejection fractions was 27.4% at ED10.5-11
and 58.4% at ED13.5-14.5, the latter being within the normal range fo
r the adult rodent heart. These methods will be useful for assessing i
n vivo cardiac function at ED10.5 and older murine embryos in litters
of transgenic or gene-targeted mice when the mutation leads to later e
mbryonic lethality.