Thromb Haemost 1993; 70(06): 1005-1008
DOI: 10.1055/s-0038-1649715
Original Article
Fibrinolysis
Schattauer GmbH Stuttgart

Effect of Isotretinoin on Endogenous Tissue-Type Plasminogen Activator (t-PA) and Plasminogen Activator Inhibitor 1 (PAI-1) in Humans

A E Wallnöfer
1   The Centre for Human Drug Research, University Hospital Leiden, The Netherlands
,
J M T van Griensven
1   The Centre for Human Drug Research, University Hospital Leiden, The Netherlands
,
H C Schoemaker
1   The Centre for Human Drug Research, University Hospital Leiden, The Netherlands
,
A F Cohen
1   The Centre for Human Drug Research, University Hospital Leiden, The Netherlands
,
W Lambert
2   The Medical-Biochemical Laboratory, State University of Gent, Belgium
,
C Kluft
3   The Gaubius Laboratory IVVO-TNO Leiden, The Netherlands
,
P Meijer
3   The Gaubius Laboratory IVVO-TNO Leiden, The Netherlands
,
T Kooistra
3   The Gaubius Laboratory IVVO-TNO Leiden, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 28 April 1993

Accepted after revision 14 July 1993

Publication Date:
06 July 2018 (online)

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Summary

The effect of isotretinoin on fibrinolysis was investigated in 10 healthy, male volunteers in a randomized, double-blind, crossover-designed study. Isotretinoin (40 mg) was administered in the morning and in the evening for 5 days. t-PA, u-PA and PAI-1 antigen and activity in plasma were measured every morning at 9 a.m. on days 1 to 4 and every 3 hours over 24 hours on day 5. Isotretinoin treatment had no significant stimulatory effect on endogenous t-PA antigen and activity in morning plasma samples nor on their circadian variation. Also, u-PA antigen levels did not change after isotretinoin treatment. Mean PAI-1 antigen and PAI activity in 9 a.m. plasma samples were non-significantly higher during isotretinoin than during placebo treatment. After treatment with isotretinoin a significant rise of fasting triglyceride plasma levels was observed as compared to placebo. The study shows that isotretinoin has no clinically significant effect on endogenous fibrinolysis.