Thromb Haemost 1967; 17(01/02): 112-119
DOI: 10.1055/s-0038-1654086
Originalarbeiten - Original Articles - Travaux Originaux
Schattauer GmbH

Effect of Temperature, Velocity Gradient and I.V. Heparin on in Vitro Blood Coagulation and Platelet Aggregation[*]

L Dintenfass**
1   Department of Medicine, University of Sydney, Sydney, and the Clinical Research Unit, Royal Prince Alfred Hospital, Sydney
,
M. C Rozenberg***
1   Department of Medicine, University of Sydney, Sydney, and the Clinical Research Unit, Royal Prince Alfred Hospital, Sydney
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
26. Juni 2018 (online)

Summary

A study of blood coagulation was carried out by observing changes in the blood viscosity of blood coagulating in the cone-in-cone viscometer. The clots were investigated by microscopic techniques.

Immediately after blood is obtained by venepuncture, viscosity of blood remains constant for a certain “latent” period. The duration of this period depends not only on the intrinsic properties of the blood sample, but also on temperature and rate of shear used during blood storage. An increase of temperature decreases the clotting time ; also, an increase in the rate of shear decreases the clotting time.

It is confirmed that morphological changes take place in blood coagula as a function of the velocity gradient at which such coagulation takes place. There is a progressive change from the red clot to white thrombus as the rates of shear increase. Aggregation of platelets increases as the rate of shear increases.

This pattern is maintained with changes of temperature, although aggregation of platelets appears to be increased at elevated temperatures.

Intravenously added heparin affects the clotting time and the aggregation of platelets in in vitro coagulation.

* Supported by a grant from the National Heart Foundation of Australia.


** Senior Research Fellow, Department of Medicine, University of Sydney, Sydney, Australia.


*** Research Fellow, Clinical Research Unit, Royal Prince Alfred Hospital, Sydney, Australia.


 
  • References

  • 1 Dintenfass L. Thixotropy of blood and proneness to thrombus formation. Circulât. Res 11: 233 1962;
  • 2 Dintenfass L. Viscosity and clotting of blood in venous thrombosis and coronary occlusions. Circulât. Res 14: 1 1964;
  • 3 Dintenfass L. A study in rheology of blood clotting in human subjects. Proc. IV. Intern. Congress Rheology 593 J. Wiley; New York: 1964
  • 4 Dintenfass L. Effect of velocity gradient on the clotting time of blood and on the consistency of clots formed in vitro. Circulât. Res 18: 349 1966;
  • 5 Rozenberg M, Dintenfass L. Thrombus formation in vitro : a rheological and morphological study. Austr. J. exp. Biol. med. Sci 42: 109 1964;
  • 6 Dintenfass L, Rozenberg M. The influence of the velocity gradient on in vitro blood coagulation and artificial thrombosis. J. Atheroscler. Res 5: 276 1965;
  • 7 Rozenberg M, Dintenfass L. Platelet aggregation in Waldenstrom’s macroglobulinaemia. Thrombos. Diathes. haemorrh. (Stuttg.) 14: 202 1965;
  • 8 Dintenfass L. An application of a cone-in-cone viscometer to the study of viscosity, thixotropy and clotting of blood. Biorheology 1: 91 1963;
  • 9 Dintenfass L. Some observations on the viscosity of pathological human blood plasma. Thrombos. Diathes. haemorrh. (Stuttg.) 13: 492 1965;
  • 10 Poole J. G. F. A study of artificial thrombi produced by a modification of Chandler’s method. Quart. J. exp. Physiol 44: 377 1959;
  • 11 Smith R. T. A heparin-precipitable fraction of human plasma. II. Occurence and significance of the fraction in normal individuals and in various disease states. J. clin. Invest 36: 605 1957;