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The Annals of Thoracic Surgery, Vol 57, 1066-1074, Copyright © 1994 by The Society of Thoracic Surgeons
RB Hird, FA Crawford Jr, R Mukherjee, MR Zile and FG Spinale
The use of protamine sulfate in patients has been associated with severe
circulatory collapse and myocardial failure. However, the exact mechanisms
responsible for these reactions to protamine remain unclear. Accordingly,
we examined the effect of protamine on isolated myocyte contractile
function. Indexes of isolated myocyte contractile function, percent
shortening, and velocity of shortening were examined using videomicroscopy.
Porcine cardiocytes (n = 75) were studied at baseline and in the presence
of 80 micrograms/mL protamine. In addition, myocyte function was examined
sequentially, first during treatment with 8 IU/mL heparin and then after
the addition of a protamine dose sufficient to completely bind the heparin.
The binding of heparin and protamine resulted in the formation of a
heparin-protamine complex. The protamine concentration of 80 micrograms/mL
is approximately equal to the serum concentration of protamine obtained in
patients when administered in a dose of 5 mg/kg. In the presence of 80
micrograms/mL protamine, both percent shortening and velocity of shortening
fell by more than 32% from baseline values (p < 0.05). The presence of
either heparin alone or the heparin-protamine complex resulted in no change
in baseline myocyte contractile measurements. Furthermore, to examine the
effect of protamine on myocyte beta-adrenergic responsiveness a second
series of experiments were performed. Myocyte contractile function was
measured when 25 nmol/L isoproterenol was added to each of the protocols
above. The presence of 80 micrograms/mL protamine resulted in a significant
blunting of myocyte beta-adrenergic responsiveness. The presence of either
heparin alone or the heparin-protamine complex resulted in no change in
myocyte beta-adrenergic responsiveness.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Effects of protamine on myocyte contractile function and beta- adrenergic responsiveness
Division of Cardiothoracic Surgery, Medical University of South Carolina, Charleston 29425.
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