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The Annals of Thoracic Surgery, Vol 54, 852-859, Copyright © 1992 by The Society of Thoracic Surgeons
JC Stringham, KL Paulsen, JH Southard, BL Fields and FO Belzer
Contracture of the arrested myocardium during prolonged storage of the
heart results in both systolic and diastolic dysfunction, and is a major
limitation to extended preservation. We studied the effects of a reversible
contractile inhibitor, 2,3-butanedione monoxime (BDM), on myocardial
ischemic tolerance. Isolated rabbit hearts were flushed with University of
Wisconsin (UW) solution with and without 30 mmol/L BDM and 1 mmol/L CaCl,
stored at 4 degrees C for 24 hours, and subsequently reperfused for 60
minutes. Left ventricular pressure-volume relationships and adenine
nucleotide content were determined before reperfusion. Left ventricular
systolic pressure, diastolic volume, and adenine nucleotide content were
measured after reperfusion. Hearts stored in UW solution underwent
contracture and adenosine triphosphate (ATP) depletion during storage, and
exhibited systolic dysfunction, impaired diastolic relaxation, and poor ATP
regeneration upon reperfusion. The addition of calcium worsened contracture
and ATP depletion (p < 0.005) and slightly improved function and ATP
regeneration (p = not significant). Hearts stored in the presence of BDM
experience no contracture during storage; ATP was preserved (10.7 versus
15.7 nmol/mg; p < 0.05), and left ventricular systolic pressure and ATP
content recovered to 74% and 93% of control on reperfusion, respectively (p
< 0.005). Left ventricular diastolic volume remained depressed, however,
although less than with UW solution (0.87 versus 0.45 mL; p < 0.001).
When both BDM and calcium were included in the UW solution,
calcium-stimulated ATP hydrolysis and contracture were prevented, left
ventricular systolic pressure returned to 87% of control, and left
ventricular diastolic volume and ATP content returned to control
levels.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Improved myocardial ischemic tolerance by contractile inhibition with 2,3-butanedione monoxime
Department of Surgery, University of Wisconsin Hospitals and Clinics, Madison 53792-3236.
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