Things that thin the blood Flashcards
Aspirin
Irreversibly inhibits COX-1 - inhibits formation thromboxane A2 in platelets, thus inhibiting platelet aggregation
COX is inhibited for the lifespan of the platelet so 7-10 days
Clopidogrel
The active metabolite irreversibly blocks the P2Y12 component of ADP receptors on the platelet surface
–>prevents activation of the GPIIb/IIIa receptor complex, thereby reducing platelet aggregation.
Platelets blocked by clopidogrel are affected for the remainder of their lifespan (~7-10 days).
Prasugrel
Prodrug that is metabolised to both active (R-138727) and inactive metabolites.
The active metabolite irreversibly blocks the P2Y12 component of ADP receptors on the platelet, which prevents activation of the GPIIb/IIIa receptor complex, thereby reducing platelet activation and aggregation
Enoxaparin
Enoxaparin binds to antithrombin to form a complex that irreversibly inactivates clotting factor Xa.
It has less activity against factor IIa (thrombin) compared to unfractionated heparin (UFH) due to its low molecular weight.
Unfractionated heparin
Potentiates the action of antithrombin III and thereby inactivates thrombin (as well as activated coagulation factors IX, X, XI, XII, and plasmin) and prevents the conversion of fibrinogen to fibrin
heparin also stimulates release of lipoprotein lipase (lipoprotein lipase hydrolyzes triglycerides to glycerol and free fatty acids)
Rivaroxaban
Factor Xa inhibitor
competitive reversible antagonist
Apixaban
Factor Xa inhibitor
reversible direct
Dabigatran
reversible, direct thrombin inhibitor that inhibits both free and fibrin-bound thrombin.
Inhibits coagulation by preventing thrombin-mediated effects, including cleavage of fibrinogen to fibrin monomers, activation of factors V, VIII, XI, and XIII, and inhibition of thrombin-induced platelet aggregation.
Abciximab
Monoclonal Ab binds to platelet IIb/IIIa receptors, resulting in steric hindrance, thus inhibiting platelet aggregation
Ticagrelor
Reversibly and non competitively binds the adenosine diphosphate (ADP) P2Y12 receptor on the platelet surface which prevents ADP-mediated activation of the GPIIb/IIIa receptor complex thereby reducing platelet aggregation.
Due to the reversible antagonism of the P2Y12 receptor, recovery of platelet function is likely to depend on serum concentrations of ticagrelor and its active metabolite.
Bivalirudin
specific and reversible direct thrombin inhibitor
binds both circulating and clot-bound thrombin
preventing thrombin-mediated cleavage of fibrinogen to fibrin monomers, and activation of factors V, VIII, and XIII.
Shows linear dose- and concentration-dependent prolongation of ACT, aPTT, PT, and TT.
Dipyridamole
inhibitors of PDE, an enzyme that catalyzes the hydrolysis of the cyclic nucleotides cAMP and cGMP
Why is GPIIbIIIa important in clotting?
When activated, platelets release thromboxane and ADP. This acts in autocrine and paracrine way on other platelets so that membrane bound IIb and IIIa merge. They can then grab on to fibrinogen (factor I) and if more than one plt grabs on to the same bit of factor, helps form clot.
Argatroban
Direct thrombin inhibitor
Danaparoid
Factor Xa inhibitors