CC BY-NC-ND 4.0 · Thromb Haemost 2017; 117(09): 1714-1721
DOI: 10.1160/TH17-03-0196
Coagulation and Fibrinolysis
Schattauer GmbH

Colistin dampens fibrinolysis and endothelial activation during endotoxaemia

A randomised, double blind trial
Christian Schoergenhofer
1   Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria
,
Peter Matzneller
1   Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria
,
Marion Mußbacher
2   Department of Vascular Biology and Thrombosis Research, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria
,
Johannes A. Schmid
2   Department of Vascular Biology and Thrombosis Research, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria
,
Petra Jilma-Stohlawetz
3   Department of Laboratory Medicine, all at Medical University of Vienna, Vienna, Austria
,
Markus Zeitlinger
1   Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria
,
Bernd Jilma
1   Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria
› Author Affiliations
Further Information

Publication History

Received: 20 March 2017

Accepted after major revision: 20 May 2017

Publication Date:
28 November 2017 (online)

Summary

Colistin electrostatically interacts with lipopolysaccharides (LPS). Preclinical studies demonstrated beneficial effects of colistin on LPS-induced coagulation and fibrinolysis. The objective of this trial was to investigate the effects of colistin during experimental endotoxaemia. In this randomised, double-blind, placebo-controlled, crossover trial 16 healthy volunteers received a 2 ng/kg LPS bolus after infusion of 2.5 million IU colistin or placebo. Plasma levels of F1+2 prothrombin fragments, thrombin-antithrombin complexes (TAT), von Willebrand factor antigen levels (vWF), E-selectin, plasmin-antiplasmin complexes (PAP), tissue-type plasminogen activator (t-PA) antigen and activity, plasminogen activator inhibitor-1 (PAI-1) were measured. Infusion of colistin significantly reduced peak concentrations of PAP complexes by 70 %, t-PA antigen levels by 63 % and t-PA activity by 48 %, while PAI-1 levels decreased numerically by 63 %. Two hours after the LPS bolus F1+2 levels and TAT complexes were slightly reduced in the colistin period, but peak concentrations were similar in both periods. Colistin blunted the LPS induced four-fold increase in soluble E-Selectin levels by ∼50 % and the two-fold increase in vWF antigen levels by ∼70 %. The LPS-scavenging actions of colistin significantly reduce endothelial activation and fibrinolytic response in the human endotoxaemia model, while the activation of the coagulation system remains largely unaffected.

Note: This work was conducted at the Medical University of Vienna.

EudraCT-Nr.: 2014–00285720

Supplementary Material to this article is available online at http://www.thrombosis-online.com

 
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