<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Reiner, Martin F.</dc:creator>
  <dc:creator>Akhmedov, Alexander</dc:creator>
  <dc:creator>Stivala, Simona</dc:creator>
  <dc:creator>Keller, Stephan</dc:creator>
  <dc:creator>Gaul, Daniel S.</dc:creator>
  <dc:creator>Bonetti, Nicole R.</dc:creator>
  <dc:creator>Savarese, Gianluigi</dc:creator>
  <dc:creator>Glanzmann, Martina</dc:creator>
  <dc:creator>Zhu, Cuicui</dc:creator>
  <dc:creator>Ruf, Wolfram</dc:creator>
  <dc:creator>Yang, Zhihong</dc:creator>
  <dc:creator>Matter, Christian M.</dc:creator>
  <dc:creator>Lüscher, Thomas F.</dc:creator>
  <dc:creator>Camici, Giovanni G.</dc:creator>
  <dc:creator>Beer, Juerg H.</dc:creator>
  <dc:date>2017-01-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The P2Y12 antagonist ticagrelor reduces mortality in patients with acute coronary  syndrome (ACS), compared with clopidogrel, and the mechanisms underlying this  effect are not clearly understood. Arterial thrombosis is the key event in ACS;  however, direct vascular effects of either ticagrelor or clopidogrel with focus on arterial  thrombosis and its key trigger tissue factor have not been previously  investigated.Methods and results: Human aortic endothelial cells were treated with  ticagrelor or clopidogrel active metabolite (CAM) and stimulated with tumour necrosis  factor-alpha (TNF-α); effects on procoagulant tissue factor (TF) expression and  activity, its counter-player TF pathway inhibitor (TFPI) and the underlying mechanisms  were determined. Further, arterial thrombosis by photochemical injury of the common  carotid artery, and TF expression in the murine endothelium were examined in  C57BL/6 mice treated with ticagrelor or clopidogrel. Ticagrelor, but not CAM, reduced  TNF-α-induced TF expression via proteasomal degradation and TF activity,  independently of the P2Y12 receptor and the equilibrative nucleoside transporter 1  (ENT1), an additional target of ticagrelor. In C57BL/6 mice, ticagrelor prolonged time to  arterial occlusion, compared with clopidogrel, despite comparable antiplatelet effects. In  line with our in vitro results, ticagrelor, but not clopidogrel, reduced TF expression in  the endothelium of murine arteries.Conclusion: Ticagrelor, unlike clopidogrel, exhibits  endothelial-specific antithrombotic properties and blunts arterial thrombus formation.  The additional antithrombotic properties displayed by ticagrelor may explain its greater  efficacy in reducing thrombotic events in clinical trials. These findings may provide the  basis for new indications for ticagrelor.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305563</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305563/files/yan_tnc.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305563/files/yan_tnc_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/cvr/cvw233</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Cardiovascular Research. - 2017, vol. 113, no. 1, p. 61–69</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Ticagrelor, but not clopidogrel, reduces arterial thrombosis via endothelial tissue factor suppression</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
