Thromb Haemost 1985; 54(02): 466-468
DOI: 10.1055/s-0038-1657874
Original Article
Schattauer GmbH Stuttgart

Increased PA-Inhibitor Levels in the Postoperative Period – No Cause-Effect Relation with Increased Cortisol

M F Aillaud
1   The Laboratory of Haematology, Hospital Timone, University of Marseille, France
,
I Juhan-Vague
1   The Laboratory of Haematology, Hospital Timone, University of Marseille, France
,
M C Alessi
1   The Laboratory of Haematology, Hospital Timone, University of Marseille, France
,
M Marecal
1   The Laboratory of Haematology, Hospital Timone, University of Marseille, France
,
M F Vinson
2   The Dept. of Surgery, Hospital Timone, University of Marseille, France
,
C Arnaud
1   The Laboratory of Haematology, Hospital Timone, University of Marseille, France
,
P Vague
3   The Dept. of Diabetology, Hospital Michel Levy, University of Marseille, Marseille, France
,
D Collen
4   The Center of Thrombosis and Vascular Research, University of Leuven, Belgium
› Author Affiliations
Further Information

Publication History

Received 12 February 1985

Accepted 15 May 1985

Publication Date:
18 July 2018 (online)

Summary

It has been reported that the level of PA-inhibitor increases in postoperative patients and on the other hand that glucocorticoids increase the PA-inhibitor level in cell culture. Because surgery is associated with increased plasma cortisol level, a relation between the postoperative increase in plasma cortisol and PA-inhibitor levels was looked for.

Blood samples were collected from 8 patients undergoing extensive abdominal surgery, before operation and postoperatively at 2 hr, 4 hr, 24 hr and daily for 7 days. Plasma cortisol and PA-inhibitor were increased 2 hr after surgery, when there was a significant correlation (p <0.05). The maximum increase was at 24 hr and the values fell to normal on day 6. An increase in t-PA related antigen (t-PA R:Ag) and a decrease in euglobulin fibrinolytic activity (EFA) also occurred.

In 7 controls 0.25 mg ACTH was given intravenously and blood was collected after ½, 1, 2, 4, 6 hr. Although the increase in plasma cortisol level following ACTH was comparable to that observed after surgery the increase was not associated with significant change in PA-inhibitor level, t-PA R: Ag or EFA.

A cause-effect relationship between the increased plasma cortisol and PA-inhibitor level could not be shown. The mechanism of the postoperative increase in PA-inhibitor thus remains unknown.

 
  • References

  • 1 Chmielewska J, Ranby M, Wiman B. Evidence for a rapid inhibitor to tissue plasminogen activator in plasma. Thromb Res 1983; 31: 427-436
  • 2 Verheijen JH, Chang GT G, Mullaart E. Inhibition of extrinsic(tissue-type) plasminogen activator by human plasma: evidence for the occurrence of a fast-acting inhibitor. Thromb Haemostas 1983; 50: 294 (Abstr)
  • 3 Juhan-Vague I, Moerman B, De Cock F, Aillaud MF, Collen D. Plasma levels of a specific inhibitor of tissue-type plasminogen activator (and urokinase) in normal and pathological conditions. Thromb Res 1984; 33: 523-530
  • 4 Kruithof EK O, Ransijn A, Gudinchet A, Tran-Thang C, Bachmann F. Studies on the fast-acting inhibitor of tissue-type plasminogen activator (t-PA) and urokinase (UK) in human plasma. Haemostasis 1984; 14: 38
  • 5 Juhan-Vague I, Aillaud MF, De Cock F, Philip-Joet C, Arnaud C, Serradimigni A, Collen D. The fast-acting inhibitor of tissue-type plasminogen activator is an acute phase reactant protein. Progress in fibrinolysis. Vol. VII (in press).
  • 6 Mellbring G, Dahlgren S, Wiman B. Fibrinolytic activity in patients subjected to gastro-intestinal surgery. Haemostasis 1984; 14: 143
  • 7 Crutchley DJ, Conanan LB, Maynard JP. Human fibroblasts produce inhibitor directed against plasminogen activator when treated with glucocorticoids. Ann NY Acad Sci 1981; 370: 609-616
  • 8 Jaken S, Geffen C, Black PH. Dexamethasone inhibition and phorbol myristate acetate stimulation of plasminogen activator in human embryonic lung cells. Biochem Biophys Res Commun 1981; 99: 379-384
  • 9 Coleman PL, Barouski PA, Gelehrter TD. The dexamethasone induced inhibitor of fibrinolytic activity in hepatoma cell. J Biol Chem 1982; 257: 4260-4267
  • 10 Gelehrter TD, Barouski-Miller PA, Coleman PL, Cwikel BJ. Hormonal regulation of plasminogen activator in rat hepatoma cells. Mol Cell Biochem 1983; 53/54: 11-21
  • 11 Gelehrter TD, Coleman PL, Cwikel BJ. Glucocorticoid induction of an inhibitor of plasminogen activator in hepatoma cells. Haemostasis 1984; 14: 94
  • 12 Mayer M, Chaouat M, Finci Z. Plasminogen activator in cultured myocytes and its response to glucocorticoid hormone. Haemostasis 1984; 14: 52
  • 13 Isacson S. Effect of prednisolone on the coagulation and fibrinolytic systems. Scand J Haematol 1970; 7: 212-216
  • 14 Oyama T. Endocrinology and the anaesthetist (Monographs in anaesthesiology). Vol 11. Elsevier; Amsterdam - New York - Oxford: 1983
  • 15 Rijken DC, Juhan-Vague I, De Cock F, Collen D. Measurement of human extrinsic plasminogen activator by a two site immuno-radiometric assay. J Lab Clin Med 1983; 101: 274-284
  • 16 Kluft C, Brakman P, Veldheyzen-Stolk EC. Screening of fibrinolytic activity in plasma euglobulin fraction on the fibrin plate. In: Progress in chemical fibrinolysis and thrombolysis. Davidson JF, Samama MM, Desnoyers PC. (eds). Vol II, 57-65 Raven Press; New York: 1976
  • 17 Von Clauss A. Gerinnungsphysiologische Schnellmethode zur Bestimmung des Fibrinogens. Acta Haematol 1957; 17: 237-247
  • 18 Rijken DC, Juhan-Vague I, Collen D. Complexes between tissue-type plasminogen activator and proteinase inhibitors in human plasma, identified with an immunoradiometric assay. J Lab Clin Med 1983; 101: 285-294
  • 19 Juhan-Vague I, Rijken DC, De Cock F, Mendez C, Collen D. Extrinsic plasminogen activator levels in clinical plasma samples. Progress in fibrinolysis. Davidson JF, Bachman F, Bouvier CA, Kruithof EKO. (eds). Vol VI, 65 69 Churchill Livingstone; Edinburgh - London - Melbourne - New York: 1983