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The Annals of Thoracic Surgery, Vol 52, 1300-1305, Copyright © 1991 by The Society of Thoracic Surgeons
M Masuda, A Demeulemeester, CC Chen, M Hendrikx, H Van Belle and W Flameng
The cardioprotective effects of a nucleoside transport inhibitor, R75231,
were investigated in the isolated rabbit heart. The hearts were subjected
to 20 minutes of global normothermic ischemia followed by reperfusion.
Before ischemia either solvent (group 1), 5 mumol/L of adenosine (group 2),
or 0.64 mg/L R75231 (group 3) was added to the perfusate. Preischemic
hemodynamics were not changed by treatment, except for an increase in
coronary flow in the adenosine group (126% of control; p less than 0.05).
Upon reperfusion, coronary flow was depressed in the controls (72% of the
preischemic control values), increased in the adenosine group (113%) and
unchanged in the R75231 group (89%). Functional recovery was significantly
better in the adenosine group as well as in the R75231 group as compared
with the controls (p less than 0.05). Cardiac output was 74% of the
preischemic control value in the R75231 group, 67% in the adenosine group,
and only 38% in the controls. Analysis of the coronary effluent after
reperfusion showed a significant inhibition of rapid release of purines and
a reverse of the adenosine/inosine ratio in the R75231 group as compared
with the others. We conclude that R75231 has a cardioprotective effect that
is probably related to accumulation of endogenous adenosine.
ARTICLES
Cardioprotective effects of nucleoside transport inhibition in rabbit hearts
Laboratory of Experimental Cardiac Surgery, Katholieke Universiteit Leuven, Leuven, Belgium.
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