Literature DB >> 26501993

Protease receptor antagonism to target blood platelet therapies.

M Holinstat1, P F Bray2.   

Abstract

Platelet activation and thrombus formation play a central role in ischemic vascular disease. Thrombin, an especially potent physiologic agonist mediating in vivo activation of platelets, acts via a unique family of G-protein-coupled receptors called protease-activated receptors (PARs) with a broad tissue expression. This review focuses on current antiplatelet therapies as well as innovative approaches to targeting PARs in patients with atherothrombotic vascular disease.
© 2015 American Society for Clinical Pharmacology and Therapeutics.

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Year:  2015        PMID: 26501993     DOI: 10.1002/cpt.282

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  3 in total

1.  The protease-activated receptor 4 Ala120Thr variant alters platelet responsiveness to low-dose thrombin and protease-activated receptor 4 desensitization, and is blocked by non-competitive P2Y12 inhibition.

Authors:  M J Whitley; D M Henke; A Ghazi; M Nieman; M Stoller; L M Simon; E Chen; J Vesci; M Holinstat; S E McKenzie; C A Shaw; L C Edelstein; P F Bray
Journal:  J Thromb Haemost       Date:  2018-11-22       Impact factor: 5.824

2.  Humanizing the Protease-Activated Receptor (PAR) Expression Profile in Mouse Platelets by Knocking PAR1 into the Par3 Locus Reveals PAR1 Expression Is Not Tolerated in Mouse Platelets.

Authors:  Shauna L French; Antonia C Paramitha; Mitchell J Moon; Ross A Dickins; Justin R Hamilton
Journal:  PLoS One       Date:  2016-10-27       Impact factor: 3.240

3.  Neutrophil cathepsin G proteolysis of protease-activated receptor 4 generates a novel, functional tethered ligand.

Authors:  Michelle L Stoller; Indranil Basak; Frederik Denorme; Jesse W Rowley; James Alsobrooks; Krishna Parsawar; Marvin T Nieman; Christian Con Yost; Justin R Hamilton; Paul F Bray; Robert A Campbell
Journal:  Blood Adv       Date:  2022-04-12
  3 in total

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