A custom-made apparatus based on a charge-coupled-device camera has been us
ed to monitor changes in fluorescence from Langendorff-perfused adult mouse
hearts stained with a voltage-sensitive dye, di-4-ANEPPS. With this approa
ch it is possible to monitor activation of the ventricles at high temporal
(375 mus/frame) and spatial resolution (72x78 pixels, 100x100 mum/pixel). I
n sinus rhythm, activation occurred with a complicated breakthrough pattern
on both ventricles, and a total activation time of 3.51+/-0.16 ms (32 degr
eesC). A stimulus applied near the apex of the left ventricle resulted in a
single activation wave front with a total activation time of 8.18+/-0.25 m
s. Pacing from a site near the middle of the left ventricular epicardial su
rface revealed anisotropic conduction, indicating that conduction occurs pr
eferentially in the direction of the predominant fiber orientation. The tot
al activation time in this configuration was 5.44+/-0.24 ms. The difference
in total activation time between sinus rhythm and epicardial stimulation s
uggests an important role for transmural conduction (the Purkinje system) i
n the mouse heart. These findings provide much of the necessary background
needed for studying conduction abnormalities in genetically altered mice an
d suggest that the comparison of sinus rhythm and epicardial pacing can be
used to reveal transmural conduction abnormalities. (C) 2000 Biomedical Eng
ineering Society. [S0090-6964(oo)01408-9].