Isolation of an active derivative produced from native streptokinase by dog plasmin.
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Biomedical subjects
Publications and source records attributed to D L Kline.
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The kidney was the primary source of plasminogen to restore normal plasma levels, after acute plasminogen depletion was produced by injection of streptokinase in cats. The concentration of plasminogen in the hepatic vein remained below that in the artery during the time when concentrations in the artery and renal vein were returning to normal.
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Improvements in preparations of tissue activator and plasminogen and termination of activation by epsilon aminocaproic acid have permitted the use of a quantitative caseinolytic assay for the measurement of the plasmin formed. The following data indicate that the activation of plasminogen by tissue activator is catalytic: a) Biphasic curve obtained when velocity was plotted against plasminogen concentration. b) First order kinetics. c) Dependence of the turnover number on tissue activator concentration. The temperature and pH stability of tissue activator were similar to those reported for urokinase. Since both of these enzymes have now been shown to activate plasminogen by a catalytic mechanism, these data support the suggestion that urokinase may be an excretory form of tissue activator which has been released into the circulation.
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