Az. Linka et al., SPONTANEOUS REDISTRIBUTION AFTER REPERFUSION - A UNIQUE PROPERTY OF AIP-201, AN ULTRASOUND CONTRAST AGENT, Journal of the American College of Cardiology, 32(6), 1998, pp. 1765-1772
Objectives. We sought to determine the mechanism of spontaneous redist
ribution of AIP 201 microbubbles after reperfusion from a single left
heart injection performed during coronary occlusion. Background. AIP 2
01, an ultrasound contrast agent consisting of 10-mu m sized microbubb
les, has demonstrated spontaneous myocardial redistribution in prelimi
nary studies. Methods. Myocardial video intensity (VI) and radiolabele
d microsphere-derived myocardial blood flow (MBF) were measured serial
ly after reperfusion in seven dogs undergoing an AIP 201 injection dur
ing coronary occlusion. The behavior of these bubbles was also assesse
d in the fat spinotrapezius muscle using intravital microscopy (IM), b
oth with and without ultrasound. The effect of ultrasound on these bub
bles was also determined in vitro. Results. A spontaneous and gradual
increase in myocardial VI was noted after reperfusion, which was relat
ed to the magnitude of increase in MBF to that region (r = 0.82, p < 0
.001), On IM, most of the microbubbles were seen entrapped in small ar
terioles. Some larger arterioles had aggregates of microbubbles that p
eriodically became dislodged and moved downstream. This behavior was n
ot affected in vivo by ultrasound. In vitro, however, microbubble aggr
egation was noted only during ultrasound exposure. Conclusions. The ma
gnitude of redistribution of AIP 201 microbubbles to the reperfused my
ocardium is related to changes in MBF and occurs from their dislodgeme
nt from microbubble aggregates entrapped in large arterioles. In vitro
microbubble aggregation seen during ultrasound exposure was not repro
duced in vivo. These results may have important implications for study
ing the effects of interventions in acute coronary syndromes and after
coronary artery bypass graft surgery. (J Am Coll Cardiol 1998;32:1765
-72) (C) 1998 by the American College of Cardiology.