Purpose: We determined whether reperfusion damage was sufficient to allow e
xtravasation of a large molecular weight contrast agent into infarcted pig
myocardium.
Material and Methods: Five pig hearts were subjected to in situ occlusion o
f the left anterior descending coronary artery (2 h) followed by reperfusio
n (1 h). The hearts were excised and perfused in the Langendorff mode for e
x vivo MR imaging. Polylysine-Gd-DTPA (50,000 Da) and Gd-DTPA. (500-700 Da)
were injected into the aorta (alternately) and followed by measurements of
T1 relaxation and mean transit time (MTT).
Results: In the normal myocardium, MTT of Gd-DTPA (56.8 +/- 23.2 s) was sig
nificantly (p=0.02) longer than that of polylysine-Gd-DTPA (29.0 +/- 7 s).
However, both normal and infarcted myocardium showed similar MTT (29.0 +/-
7.0 vs. 28.0 +/- 5.0 s, p>0.05) when using polylysine-Gd-DTPA.
Conclusion: The results indicate that the permeability of capillaries to po
lylysine-Gd-DTPA was not significantly higher in infarcted regions of the m
yocardium compared to normal tissue. However, infarcted myocardium displaye
d an increased permeability to the small molecular weight Gd-DTPA. We concl
ude that microvascular damage may not be sufficient to allow the extravasat
ion of polylysine-Gd-DTPA in infarcted myocardium.