Thromb Haemost 1981; 46(01): 043
DOI: 10.1055/s-0038-1652076
Heparin – I: Antithrombin III
Schattauer GmbH Stuttgart

The Antiheparin And Antiplatelet-Aggregating Effects Of Human α1-Acid Glycoprotein; Influence On Heparin Tolerance In Acute Phase Reactions

Authors

  • P Andersen

    Haematological Research Lab.& Central Lab, Oslo, Norway
  • P Kierulf

    Haematological Research Lab.& Central Lab, Oslo, Norway
    ×   Univ. Clinic, Ullevål Hospital, Oslo, Norway
  • H C Godal

    Haematological Research Lab.& Central Lab, Oslo, Norway
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
25. April 2019 (online)

Preview

The antiheparin effect of human α1-n-acid glycoprotein (α1-acid GP), in thrmbin clotting time systems, was originally observed after the addition of purified α1-acid GP to heparinized, citrated human plasma. The α1-acid GP used in that and other studies was rather crude. In the present study, however, a similar antiheparin effect has been observed with highly purified, non-desialyzed α1-n-acid GP. Furthermore, the inhibitory effect of this highly purified α1-acid GP on the thronbin-induced platelet aggregation was identical to that of the less purified preparation. The antiheparin effect of highly purified α1-acid GP isolated in parallel frcm pooled plasma of patients with acute phase reactions and from healthy controls was likewise identical.

In patients (n=10), with acute phase reaction, only the concentration of α1-acid GP was negatively correlated with the heparin thrcrnbin clotting time (r=0.42), indicating α1-acid GP to be a major contributor to the increased heparin tolerance observed during such disease states.

Removal of α1-acid GP by precipitating with rabbit anti- human α1-acid GP antibodies failed to danonstrate the heparin-neutralizing effect of α1-acid GP, probably because inmunoglobulins per se possess heparin-neutralizing activity.

Our findings suggest that α1-acid GP, during the acute phase reaction, interacts in a way to reduce untimely consequences of plasma hypercoagulability and/or platelet reactivity.