ASPIRIN ENHANCES THE BENEFITS OF LATE REPERFUSION ON INFARCT SHAPE - A POSSIBLE MECHANISM OF THE BENEFICIAL-EFFECTS OF ASPIRIN ON SURVIVAL AFTER ACUTE MYOCARDIAL-INFARCTION
Ia. Alhaddad et al., ASPIRIN ENHANCES THE BENEFITS OF LATE REPERFUSION ON INFARCT SHAPE - A POSSIBLE MECHANISM OF THE BENEFICIAL-EFFECTS OF ASPIRIN ON SURVIVAL AFTER ACUTE MYOCARDIAL-INFARCTION, Circulation, 91(11), 1995, pp. 2819-2823
Background The time window of the benefits of late reperfusion on infa
rct shape is limited. In rats, these benefits diminish in a wave front
over time, with minimal benefits when reperfusion follows 16 hours of
coronary occlusion. The mechanism of the benefits of aspirin on survi
val after acute myocardial infarction is unknown. The purpose of this
study was to test the ability of aspirin to enhance the benefits of la
te coronary artery reperfusion on infarct shape and to examine the mec
hanism of the benefits of aspirin on infarct shape. Methods and Result
s Rats were entered into two different protocols, the morphometric and
the histological protocols. In the morphometric protocol, rats were r
andomized into two groups: the aspirin group, in which rats underwent
left coronary artery occlusion followed by treatment with aspirin (12
mg/kg IV), and the control group, in which rats underwent left coronar
y artery occlusion followed by treatment with placebo. Rats in both gr
oups were reperfused 8 hours after coronary occlusion. Rats in the asp
irin group received aspirin in the drinking water (12+/-2 mg/kg daily)
. Morphometric analysis was performed 2 weeks after acute myocardial i
nfarction. In the histological protocol, rats underwent the same rando
mization, coronary occlusion, and reperfusion protocols. Hearts were r
emoved 24 hours after coronary occlusion, and microvessels were assess
ed for patency. Infarct size expressed as a percent of circumference w
as similar in the aspirin and placebo treatment groups (28+/-2% versus
33+/-3%, P=NS). Septal thickness was also similar in both groups (1.8
+/-0.1 versus 2.1+/-0.1 mm, P=NS for aspirin versus placebo). The aspi
rin-treated group had thicker infarcts compared with the placebo-treat
ed group (0.8+/-0.1 versus 0.5+/-0.1 mm, P<.05) and less expanded infa
rcts (expansion index, 1.2+/-0.1 versus 2.0+/-0.2, P<.05). Aspirin was
associated with increased patency of the microvessels in the infarcte
d area compared with the placebo group (96% versus 64% of microvessels
patent, P<.001). Conclusions Aspirin enhances the benefit of late cor
onary artery reperfusion on infarct shape after 8 hours of coronary oc
clusion. The benefits of aspirin on infarct shape after late reperfusi
on are related to increased patency of the microvessels in the infarct
ed area.