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Effects on blood compatibility in vitro by combining a direct P2Y12 receptor inhibitor and heparin coating of stents.
- Source :
-
Platelets [Platelets] 2006 Aug; Vol. 17 (5), pp. 318-27. - Publication Year :
- 2006
-
Abstract
- The effect of the direct platelet P2Y12 receptor inhibitor, AR-C69931MX, on activation of blood induced by stents with and without heparin coating was investigated using a whole blood Chandler loop model in vitro. Stents were deployed in Chandler loops. Fresh human blood with heparin and AR-C69931MX was rotated for 1 h at 37 degrees C and used for measurements of platelets, microparticles, thrombin-antithrombin complex (TAT), fibrinogen binding to platelets, P-selectin expression by platelets, CD11b, Prothrombin Fragment F1+2, FXIa-AT, FXIIa-AT, C3a, sC5b-9 and stent score. In the first experiment there were four study groups with unmodified stents: 1a, no AR-C69931MX; 1b, 250 nmol/L; 1c, 750 nmol/L; 1d, 2250 nmol/L of AR-C69931MX. In the second experiment the concentration of AR-C69931MX was 500 nmol/L: 2a; tubings without stent; 2b; tubings with heparin-coated stent; 2c; tubings with unmodified stents. Heparin-coated stents were used in the third experiment: 3a; no AR-C69931MX; 3b; 500 nmol/L of AR-C69931MX. In the first experiment there were significant differences in all parameters analysed except for C3a, and stent score when the group with no AR-C69931MX was compared to all the groups with AR-C69931MX. In the second experiment there were significant differences in platelet count, TAT, FXIa-AT, FXIIa-AT and stent score when unmodified stents were compared to loops with no stents and partly to loops with heparin-coated stents. In the third experiment there was a significant reduction in generation of TAT, stent score and better preservation of platelet number by combining the platelet inhibitor and heparin-coated stents as compared to heparin-coated stents alone. The conclusion is that the direct P2Y12 receptor inhibitor AR-C69931MX reduced the different aspects of activation of blood induced by both unmodified and heparin-coated stents.
- Subjects :
- Adenosine Monophosphate pharmacology
Analysis of Variance
Anticoagulants adverse effects
Anticoagulants pharmacology
Antithrombin III analysis
CD11b Antigen drug effects
Complement Activation drug effects
Drug Delivery Systems
Factor XIIa analysis
Factor XIa analysis
Flow Cytometry
Heparin administration & dosage
Heparin pharmacology
Humans
In Vitro Techniques
Membrane Proteins antagonists & inhibitors
Membrane Proteins drug effects
Peptide Hydrolases analysis
Platelet Activation physiology
Purinergic P2 Receptor Antagonists
Receptors, Purinergic P2 drug effects
Receptors, Purinergic P2Y12
Adenosine Monophosphate analogs & derivatives
Blood Platelets metabolism
CD11b Antigen metabolism
Platelet Activation drug effects
Platelet Aggregation Inhibitors pharmacology
Stents
Subjects
Details
- Language :
- English
- ISSN :
- 0953-7104
- Volume :
- 17
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Platelets
- Publication Type :
- Academic Journal
- Accession number :
- 16928604
- Full Text :
- https://doi.org/10.1080/09537100600746557