Circulation, Vol 51, 668-676, Copyright © 1975 by American Heart Association
G Autenrieth, B Surawicz, CS Kuo and M Arita
We correlated primary T wave changes with the changes of monophasic action
potentials (MAP) recorded with suction electrodes from the ventricular
surface of the dog heart following systemic or intracoronary infusions of
small doses of isoproterenol (ISP). The portions of the heart perfused with
ISP were excised and weighed to determine the mass of perfused tissue. ISP
shortened the ventricular MAP by an average of 12-18 msec in the entire
ventricular mass following systemic administration, in 34 plus or minus 6
per cent of the ventricular mass after injection into the left circumflex
coronary artery (LCA), in 8.5 plus or minus 2.6% of the ventricular mass
after injection into a branch of LCA and in 17 plus or minus 8 per cent of
the ventricular mass after injection into the right CA. The MAP changes
induced by ISP were similar to the transmembrane action potential changes
recorded with microelectrodes from papillary muscles excised from the same
dogs. The most important results of this study showed that: 1) the early
and the late effects of ISP administration produced opposite effects on the
T wave polarity. The early T wave change was associated with nonhomogeneous
and the late change with homogeneous MAP shortening; 2) the T wave change
was greater after infusion into LCA than after systemic administration, 3)
the T wave change was greater after infusion into LCA than after infusion
into LCA branch apparently because of greater mass of the ISP-perfused
myocardium; 4) the T wave change was greater after infusion into LCA branch
than after infusion into RCA, apparently due to the unequal regional
repolarization contribution to the T wave; 5) the ventricular gradient did
not always reflect the magnitude of the primary T wave change. Our study
helps to identify factors contributing to high sensitivity and low
specificity of T wave abnormalities.
ARTICLES
Primary T wave abnormalities caused by uniform and regional shortening of ventricular monophasic action potential in dog
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