Bleeding And Thrombosis Flashcards
(17 cards)
Humoral mediators in plasma
Epinephrine
Thrombin
Mediators released from activated platelets
adenosine diphosphate, serotonin
and vessel wall
extracellular matrix constituents that come in contact with adherent
platelets
Collagen, vWF
most
abundant receptor on the platelet surface.
Gp) IIb/IIIa (αIIbβ3
We now know that coagulation is normally initiated through
tissue factor (TF) exposure and activation through
the classic extrinsic
pathway but with critically important amplification through elements
of the classic intrinsic pathway,
TF is constitutively expressed on the surfaces
of
subendothelial cellular components of the vessel wall, such as
smooth muscle cells and fibroblasts.
pivotal protease of the
coagulation system.
Thrombin
multifunctional
enzyme that converts soluble plasma fibrinogen to an insoluble fibrin matrix
Thrombin
covalently cross-links
and thereby stabilizes the fibrin clot.
Factor 13a
acts as an anticoagulant by cleaving and inactivating activated factors
V and VIII.
Activated protein C, accelerated by a cofactor, protein S,
cleaves the N-terminal lysine residues
of fibrin, which aid in localization of plasmin activity
thrombin-activatable fibrinolysis inhibitor (TAFI
primary inhibitor
of tPA and uPA in plasma.
plasminogen activator inhibitors (PAI-1)
main inhibitor of plasmin in human plasma, inactivating any
nonfibrin clot–associated plasmin.
α2-antiplasmin
inhibit platelet binding, secretion, and
aggregation.
antithrombotic
effects. They produce prostacyclin, nitric
oxide, and ectoADPase/CD39,
activate
fibrinolytic mechanisms through the pro-
duction of tissue plasminogen activator,
urokinase, plasminogen activator inhibi-
tors, and annexin-2.
anticoagulant factors including hepa-
ran proteoglycans, TF pathway inhibitor,
and thrombomodulin.
neutralizes
thrombin and other activated coagulation factors by forming a com-
plex between the active site of the enzyme and its reactive center
Antithrombin
hallmark of moderate and severe factor VIII and
IX deficiency and, in rare circumstances, of other clotting factor
deficiencies
Spontaneous
hemarthroses