DIFFERENCES IN REPERFUSION LENGTH FOLLOWING 30 MINUTES OF ISCHEMIA INTHE RABBIT INFLUENCE INFARCT SIZE, AS MEASURED BY TRIPHENYLTETRAZOLIUM CHLORIDE STAINING
Y. Birnbaum et al., DIFFERENCES IN REPERFUSION LENGTH FOLLOWING 30 MINUTES OF ISCHEMIA INTHE RABBIT INFLUENCE INFARCT SIZE, AS MEASURED BY TRIPHENYLTETRAZOLIUM CHLORIDE STAINING, Journal of Molecular and Cellular Cardiology, 29(2), 1997, pp. 657-666
Assessment of myocardial infarct size in acute experimental models is
usually done by triphenyltetrazolium-chloride (TTC) staining. A certai
n period of reperfusion is mandatory for discrimination of the infarct
zone, especially after relatively short ischemic periods. However, it
is unclear what the optimal reperfusion time is for full delineation
of the infarct following 30 min of myocardial ischemia in the rabbit.
This study compares infarct size, assessed by TTC, in anesthetized ope
n-chest rabbits subjected to 30 min of coronary artery occlusion follo
wed by either 2 (n=14) v 4 (n=14) (protocol 1), or 3 (n=8) v 6 (n=7) h
of reperfusion (protocol 2). Area at risk was assessed by blue dye an
d necrotic zone by TTC staining. Protocol 1: heart rate and mean blood
pressure were comparable in both groups throughout the protocol. Regi
onal myocardial blood flows in both the ischemic and non-ischemic zone
s during ischemia and after 2 h of reperfusion were comparable between
the groups. Regional myocardial blood now in the post-ischemic zone d
eteriorated between 2 and 4 h (1.11+/-0.15 v 0.58+/-0.09 ml/min/g, res
pectively; P=0.0004) of reperfusion. The size of the area at risk was
comparable (0.31+/-0.03 v 0.33+/-0.03 of the LV weight in the 2 and 4
h reperfusion groups). However, the ratio of the necrotic zone to the
ischemic zone at risk was 63% larger in the 4 compared to the 2h of re
perfusion group (0.31+/-0.04 v 0.19+/-0.03, respectively, P=0.02). Ana
lysis of covariance performed on the weight of tissue that developed n
ecrosis and the weight of ischemic zone at risk revealed a significant
effect of the reperfusion time (P=0.014), Protocol 2: there was no di
fference in infarct size between rabbits subjected to three (0.38+/-0.
05 of the area at risk) v 6h (0.41+/-0.07) of reperfusion (P=0.72). An
alysis of covariance performed on the weight of tissue that developed
necrosis and the weight of ischemic zone at risk did not reveal a sign
ificant effect of the reperfusion time. Infarct size as assessed by TT
C following 30 min of myocardial ischemia, is smaller when measured 2
h after reperfusion than after 4 h of reperfusion. At least 3 h of rep
erfusion is needed to delineate infarct size by tetrazolium staining f
ollowing 30 min of ischemia. (C) 1997 Academic Press Limited.