A. Bauer et al., Effects of propafenone on anisotropic conduction properties within the three-dimensional structure of the canine ventricular wall, BAS R CARD, 96(2), 2001, pp. 175-183
Background Structural complexities of the intact ventricular wall cause a v
ery complex spread of activation. The effects of regional tissue damage and
of antiarrhythmic drugs on directional differences in activation should he
lp to further elucidate intramural conduction patterns.
Methods and results In 10 healthy dogs and in 5 dogs with subacute anterior
wall infarction, 6 parallel rows of 6 needle electrodes with 4 bipolar ele
ctrode pairs per needle were inserted into the left anterior ventricular wa
ll. Using a computerized multiplexer-mapping system, the spread of activati
on in epi-, endo- and midmyocardial muscle layers and in the surviving epic
ardium, respectively, was reconstructed. Marked differences in conduction v
elocities relative to fiber orientation were evident in the surviving epica
rdium of infarcted hearts. Directional differences in conduction velocities
, although less pronounced, were still preserved throughout the intact vent
ricular wall. Epicardial transverse conduction in intact hearts was signifi
cantly faster than transverse conduction in infarcted hearts (0.87 +/- 0.11
m/s vs 0.68 +/- 0.1 m/s). In normal hearts, propafenone (2 mg/kg) decrease
d conduction velocities primarily in longitudinal directions (-27 +/- 10 %)
, but also moderately in transverse directions (-13 +/- 7 %) of all muscle
layers, with no significant effect on straight (-4 +/- 8 %), but on oblique
transmural conduction (-33 +/- 18 %). In infarcted hearts propafenone decr
eased conduction particularly in longitudinal direction (-23 +/- 14 %) with
out affecting conduction transverse to the fiber orientation (+3 +/- 6%).
Conclusions Longitudinal intramural shortcircuits reduce directional differ
ences in activation. Transmural infarction results in a loss of alternative
intramural pathways, unmasking marked anisotropy in the surviving epicardi
um. Conduction delay in intramural pathways explains the effects of propafe
none on transverse and oblique transmural conduction. Primarily longitudina
l conduction delay results in reduced tissue anisotropy.