Inhibitors Interfering with the Quantitative Estimation of Tissue Plasminogen Activator

1975 ◽  
Author(s):  
G. Wijngaards ◽  
A. T. Potjer

The commonly used quantitative assay for plasminogen activator in tissues by Astrup and Albrechtsen (1957) was re-evaluated with special reference to the presence of inhibitors in tissue extracts at different stages of the procedure.Human lung, liver, and placenta tissues were chosen for their different activator and inhibitor content. Samples of the extracts were tested for inhibitory capacity against purified human tissue plasminogen activator, urokinase, and plasmin on different kinds of fibrin plates.The procedure for preparing the samples according to Astrup and Albrechtsen did not completely eliminate the inhibitory action against the plasminogen activators added. The presence of inhibitors was partly obscured by 2M KCNS in the sample. In order to quantitate the plasminogen activator content in tissues, the method should be revised with respect to the elimination of inhibiting material.Some interesting aspects of the inhibitory components extracted from liver and placenta were revealed by comparing urokinase inhibition to tissue activator inhibition as to the degree of denaturation during the procedure. It was suggested that, although they have much in common, urokinase and tissue activator inhibitors are separate entities.

1979 ◽  
Vol 41 (03) ◽  
pp. 590-600 ◽  
Author(s):  
G Wijngaards

SummaryThe assay of plasminogen activator activities on fibrin plates was re-evaluated with special reference to fibrinolysis inhibitors present in samples and in fibrin plates. The nature, action and stability of inhibiting material were studied in tissues with considerable differences in activator and inhibitor contents! human lung, liver and placenta. Extracts were tested for inhibitory capacity against purified human uterine tissue plasminogen activator, urokinase and plasmin on fibrin plates prepared from different grades of fibrinogens and fibrin.The tissue extracts inhibited fibrinolysis on fibrin plates to varying degrees, dependent on the sample medium, the type of fibrin plate and the kind of plasminogen activator. The influence of inhibitors in the sample and in the fibrin plate was partly abolished by the presence of 2 M KSCN in the sample. The procedure for preparing the samples as described by Astrup and Albrechtsen did not completely eliminate the inhibitory action against the added plasminogen activators.Comparison of urokinase inhibition with tissue activator inhibition by the tissue extracts as to the degree of denaturation in the Astrup and Albrechtsen procedure showed that they have much in common. Nevertheless, some differences were found which indicated the possible existence of separate urokinase and tissue activator inhibitors or of different inhibition mechanisms for these plasminogen activators.


2007 ◽  
Vol 10 (6) ◽  
pp. 946-949 ◽  
Author(s):  
Hamid Mir Mohammad S ◽  
Kianoush Dormiani ◽  
Yahya Khazaie ◽  
Mohammad Rabbani ◽  
Fatemeh Moazen

1989 ◽  
Vol 7 (5) ◽  
pp. 495-501 ◽  
Author(s):  
Paolo Sarmientos ◽  
Marc Duchesne ◽  
Patrice Denèfle ◽  
Janine Boiziau ◽  
Nadine Fromage ◽  
...  

1983 ◽  
Vol 80 (2) ◽  
pp. 349-352 ◽  
Author(s):  
T. Edlund ◽  
T. Ny ◽  
M. Ranby ◽  
L. O. Heden ◽  
G. Palm ◽  
...  

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