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The Heart Institute, Good Samaritan Hospital, University of Southern California, Los Angeles, California 90017-2395
No reflow
after acute myocardial infarction is an important predictor of infarct
size and clinical outcome. However, the exact relationship between no
reflow and infarct size remains to be determined, particularly because
no reflow may progress during the time course of reperfusion. Control
groups of five previous protocols using the anesthetized, open-chest
rabbit model of coronary artery occlusion and reperfusion were
retrospectively analyzed with respect to the correlation between
regional myocardial blood flow (RMBF; radioactive microspheres) and
infarct size (triphenyltetrazolium chloride) in the course of
reperfusion. After 30 min of occlusion, reflow (defined as the ratio of
RMBF in the risk area divided by the nonischemic area) declined
from hyperemic values after 30 min of reperfusion (reflow ratio:
1.33 ± 0.81; RMBF in the risk area at the same time point:
2.25 ± 1.04 ml · g
1 · min
1) to
0.47 ± 0.22 after 120 min and 0.46 ± 0.13 after 180 min of reperfusion. After 120 min of ischemia, reflow at 30 min of
reperfusion was 0.49 ± 0.24 and deteriorated by 120 min of
reperfusion (0.26 ± 0.15). In every group, there was a strong
correlation between infarct size and reflow (correlation coefficients:
0.62 to
0.82). The lines of regression for the groups with
assessment of RMBF after 120 or 180 min of reperfusion were nearly
identical regardless of the duration of ischemia. Thus
microvascular reperfusion injury led to a striking decrease in RMBF
within the first 2 h of reperfusion, with infarct size as the
major determinant of reflow at a given time point of reperfusion.
myocardial blood flow; rabbit; microvasculature
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