Circulation, Vol 79, 179-187, Copyright © 1989 by American Heart Association
D Rovai, A L'Abbate, M Lombardi, SE Nissen, M Marzilli, A Distante, EM Ferdeghini and AN DeMaria
This study was performed to examine the transmural (endocardial vs.
epicardial) heterogeneity of myocardial blood flow during the cardiac cycle
(systole vs. diastole). Twenty-four contrast echocardiographic injections
were performed in seven open-chest anesthetized dogs either into left
anterior descending or circumflex coronary artery or into the aortic root.
Two-dimensional echocardiography in short-axis view was performed and was
digitized off-line into a 256 x 256 pixel matrix with 256 gray
levels/pixel. All end-diastolic and end-systolic frames before and to peak
contrast were analyzed. A region of interest corresponding to the most
intensely opacified myocardial segment was traced, the mean videodensity
measured, and the frame of initial contrast appearance detected. The region
of interest was divided into three equal parallel layers corresponding to
the endocardial, midcardial, and epicardial myocardium. When the
echocardiographic contrast effect initially appeared in diastole, the
increment in videodensity was greater for the endocardium (131 +/- 48%)
than for the epicardium (71 +/- 37% of the increment in videodensity of the
entire wall) (p less than 0.05). This inhomogeneity subsequently
disappeared in the following end-systolic frame. When the initial
echocardiographic contrast effect appeared in systole, intensity was higher
in epicardium (136 +/- 83%) than in endocardium (60 +/- 60%) (p less than
0.05). However, in the following diastole, intensity was not significantly
different for the two layers. Thus, myocardial contrast echocardiography
demonstrates that coronary blood flow is primarily subendocardial in
distribution during diastole and subepicardial during systole.
ARTICLES
Nonuniformity of the transmural distribution of coronary blood flow during the cardiac cycle. In vivo documentation by contrast echocardiography
CNR Clinical Physiology Institute, University of Pisa, Italy.
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