Thromb Haemost 2005; 93(06): 1161-1167
DOI: 10.1160/TH03-09-0588
Endothelium and Vessel Development
Schattauer GmbH

Endothelial nitric oxide synthase plays a minor role in inhibition of arterial thrombus formation

Burcin Özüyaman
1   Institut für Herz- und Kreislaufphysiologie
,
Axel Gödecke
1   Institut für Herz- und Kreislaufphysiologie
,
Susanne Küsters
1   Institut für Herz- und Kreislaufphysiologie
,
Elisabeth Kirchhoff
2   Institut für Hämostaseologie und Transfusionsmedizin, Heinrich-Heine-Universität
,
Rüdiger E. Scharf
2   Institut für Hämostaseologie und Transfusionsmedizin, Heinrich-Heine-Universität
3   Biologisch Medizinisches Forschungszentrum, Düsseldorf, Germany
,
Jürgen Schrader
1   Institut für Herz- und Kreislaufphysiologie
3   Biologisch Medizinisches Forschungszentrum, Düsseldorf, Germany
› Author Affiliations
Further Information

Publication History

Received 23 September 2003

Accepted after resubmission 07 April 2005

Publication Date:
11 December 2017 (online)

Summary

Endothelial NO synthase (eNOS) expressed in the vascular en-dothelium or formed within platelets was postulated to inhibit platelet activation and aggregation. We have assessed the role of eNOS in platelet aggregation in vitro and in vivo by comparison of WT and eNOS-/- mice. Aggregometer studies revealed that collagen over a concentration range of 0.36–10 µg aggregated WT and eNOS-/- platelets to the same extent (10 µg: WT 86.7±4.7%, eNOS-/- 91±12%, n=6). Collagen treatment did not result in a significant increase in cGMP formation and VASP phosphorylation. Thrombin-induced P-selectin surface expression was unchanged in eNOS-/- platelets. In line with these findings no eNOS protein was detectable within the platelets of WT mice. In vivo, bleeding time after tail tip resection tended to be shorter in eNOS/- mice (WT: 116±35 s; eNOS-/- 109±37 s, n.s). Similarly, time to occlusion of the A.carotis after focal induction of thrombosis was 501±76 s (WT) and 457±95 s (eNOS-/-) (n.s.). These data demonstrate that eNOS-deficiency minimally affects platelet aggregation and is not associated with accelerated arterial thrombosis in vivo. Thus, in the mouse endothelial NO synthase does not play a major role in the autocrine modulation of platelet function and in thrombosis of conduit vessels in vivo.

 
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