Thromb Haemost 1991; 66(04): 468-473
DOI: 10.1055/s-0038-1646440
Review Article
Schattauer GmbH Stuttgart

Comparative Fibrinolytic Properties of Staphylokinase and Streptokinase in Animal Models of Venous Thrombosis

H R Lijnen
The Center for Thrombosis and Vascular Research, University of Leuven, Belgium
,
J M Stassen
The Center for Thrombosis and Vascular Research, University of Leuven, Belgium
,
I Vanlinthout
The Center for Thrombosis and Vascular Research, University of Leuven, Belgium
,
H Fukao
*   The Department of Physiology, Kinki University School of Medicine, Osaka, Japan
,
K Okada
*   The Department of Physiology, Kinki University School of Medicine, Osaka, Japan
,
O Matsuo
*   The Department of Physiology, Kinki University School of Medicine, Osaka, Japan
,
D Collen
The Center for Thrombosis and Vascular Research, University of Leuven, Belgium
› Author Affiliations
Further Information

Publication History

Received 11 January 1991

Accepted 22 March 1991

Publication Date:
25 July 2018 (online)

Summary

The thrombolytic and pharmacokinetic properties of staphylokinase were compared with those of streptokinase in hamsters with a pulmonary embolus produced from human plasma or from hamster plasma, and in rabbits with a jugular vein blood clot produced from rabbit blood. In both models, a continuous intravenous infusion of staphylokinase and streptokinase over 60 min in hamsters or over 4 h in rabbits, induced dose-dependent progressive clot lysis in the absence of significant systemic activation of the fibrinolytic system. The results of thrombolytic potency (clot lysis at 30 min after the end of the infusion, in percent, versus dose administered, in mg/kg) were fitted with an exponentially transformed sigmoidal function and the maximal percent clot lysis (c), the maximal rate of lysis (z = ¼ac · e b ) and the dose at which the maximal rate of lysis is achieved (b) were determined. In hamsters with a pulmonary embolus produced from human plasma, streptokinase had a somewhat higher thrombolytic potency than staphylokinase, as revealed by a higher z value (2,100 ± 1,100% lysis per mg/kg streptokinase administered versus 1,100 ± 330% lysis per mg/kg for staphylokinase). In hamsters with a pulmonary embolus produced from hamster plasma, staphylokinase had a somewhat higher thrombolytic potency than streptokinase (z = 1,600 ± 440 versus 1,200 ± 370% lysis per mg/kg). Staphylokinase had a higher thrombolytic potency than streptokinase in rabbits, as revealed by a higher z-value (950 ± 350% lysis per mg/kg staphylokinase administered versus 330 ± 39% lysis per mg/kg for streptokinase) and a lower b-value (0.035 ± 0.010 mg/kg staphylokinase versus 0.091 ± 0.008 mg/kg for streptokinase). The plasma clearance following bolus injection of staphylokinase or streptokinase in hamsters or rabbits was comparably rapid (1.1 to 1.4 ml/min in hamsters and 14 to 15 ml/min in rabbits) as a result of a short initial half-life (1.8 to 1.9 min in hamsters and 1.7 to 2.0 min in rabbits). These results in two quantitative rodent models of thrombolysis suggest that staphylokinase is a potent thrombolytic agent with an in vivo thrombolytic potency that is comparable to that of streptokinase. Further investigation of the thrombolytic potential of staphylokinase seems to be warranted.

 
  • References

  • 1 Collen D, Lijnen HR. Molecular mechanisms of thrombolysis: implications for therapy. Biochem Pharmacol 1990; 40: 177-86
  • 2 Lack CH. Staphylokinase: an activator of plasma protease. Nature 1948; 161: 559-60
  • 3 Lewis JH, Ferguson JH. A proteolytic enzyme system of the blood. III. Activation of dog serum Profibrinolysin by staphylokinase. Am J Physiol 1951; 166: 594
  • 4 Sako T. Overproduction of staphylokinase in Escherichia coli and its characterization. Eur J Biochem 1985; 149: 557-63
  • 5 Matsuo O, Okada K, Fukao H, Tomioka Y, Ueshima S, Watanuki M, Sakai M. Thrombolytic properties of staphylokinase. Blood 1990; 76: 925-9
  • 6 Lijnen HR, Van Hoef B, De Cock F, Okada K, Ueshima S, Matsuo O, Collen D. On the mechanism of fibrin-specific plasminogen activation by staphylokinase. J Biol Chem 1991; 266: 11826-32
  • 7 Sakai M, Watanuki M, Matsuo O. Mechanism of fibrin-specific fibrinolysis by staphylokinase: participation of α2-plasmin inhibitor. Biochem Biophys Res Commun 1989; 162: 830-7
  • 8 Fraker PJ, Speck Jr JC. Protein and cell membrane iodinations with a sparingly soluble chloroamide l,3,4,6-tetrachloro-3a,6a-diphenylglyceroluril. Biochem Biophys Res Commun 1978; 80: 849-57
  • 9 Stassen JM, Vanlinthout I, Lijnen HR, Collen D. A hamster pulmonary embolism model for the evaluation of the thrombolytic and pharmacokinetic properties of thrombolytic agents. Fibrinolysis 1990; 4 (Suppl 2) 15-21
  • 10 Clauss A. Gerinnungsphysiologische Schnellmethode zur Bestimmung des Fibrinogens. Acta Haematol 1957; 17: 237-46
  • 11 Edy J, Collen D, Verstraete M. Quantitation of the plasma protease inhibitor antiplasmin with the chromogenic substrate S-2251. In: Progress in Chemical Fibrinolysis and Thrombolysis. Vol. 3.. Davidson JF, Rowan RM, Samama MM, Desnoyers PC. (eds) Raven Press, New York: 1978. pp 315-22
  • 12 Collen D, Stassen JM, Verstraete M. Thrombolysis with human extrinsic (tissue-type) plasminogen activator in rabbits with experimental jugular vein thrombosis. Effect of molecular form and dose of activator, age of the thrombus, and route of administration. J Clin Invest 1983; 71: 368-76
  • 13 Gibaldi M, Perrier D. Pharmacokinetics. Marcel Dekker, New York: 1983. pp 45-111
  • 14 Sako T, Sawaki S, Sakurai T, Ito S, Yoshizawa Y, Kondo I. Cloning and expression of the staphylokinase gene of Staphylococcus aureus in E. coli. . Mol Gen Genet 1983; 190: 271-7
  • 15 Behnke D, Gerlach D. Cloning and expression in Escherichia coli, Bacillus subtilis and Streptococcus sanguis of a gene for staphylokinase – a bacterial plasminogen activator. Mol Gen Genet 1987; 210: 528-34