final lecture 3 Flashcards
important functions of hemostasis
upon damage- arrests bleeding
normally-maintains blood flow
thrombosis
forms a blot in an intact blood vessel
hemostasis & thrombosis involve 4 major components
vascular endothelium, plts, coagulation system, fibrinolytic system
each rxn results from the interactions of:
an enzyme, substrate, and cofactor
vitamin K dependent factors
II, VII, IX, X
contact activated factors/ beginning of intrinsic cascade
XII, prekallikrein, high molecular weight kininogen
thrombin sensitive factors
I-fibrinogen, V, VIII, XI, XIII
hemostasis events in response to vascular injury
localized vascular spasms, primary hemostasis, secondary hemostasis, clot dissolution
primary hemostasis
formation of primary plt plug & involves plts, blood vessel wall & von willeebrand factor
plt adhesion is mediated by ____ in primary hemostasis
von willebrand factor
Plt-plt binding is mediated by___
fibrinogen which binds to GPIIb/IIIa on adj plts
secondary hemostasis
formation of fibrin through the coagulation cascade
initiation of coagulation
extrinsic pathway aka rapid response
thrombin-sensitive factors
V, VIII, XI
secondary hemostasis actions
plt activation & aggregation, fibrinogen->fibrin, activates XIII
scope of secondary hemostasis is to:
stabilize the initial soft clot. takes longer than primary hemostasis!
plts contain COX-__ only!
one
> intracellular Ca and activation of PKC
shape change & activation, release of secretory factors, aggregation
TxA2 stimulates
activation of new platelets & favor plt aggregation
expression of negatively charged phospholipid complexes on plt surface
bind Ca & serve as assembly sites & activation for coagulation factor complexes
ADP activates
P2Y1(>Ca) & P2Y12(<cAMP)
factor XIIIa aka fibrin stabilizing factor
crosslinks firbin forming an insoluble clot (2* hemostatic plug)
tenase complex
IXa & VIIIa
activates factor X
prothrombinase complex
Xa & Va
converts prothrombin->thrombin
extrinsic pathway cascade
TF: VII->VIIa which activates X->Xa
thrombin prothrombic actions
fibrinogen->fibrin
activates PAR1 &4
activates V, VIII, and XI and XIII
thrombin anti-thrombotic effects
activates protein C (inhibits coagulation)
mutation in factor V gene ->
thrombophilia bc cannot be broken down by protein C
___ reduces vitamin K to its active form
vitamin K epoxide reductase (VKOR)
warfarin target
blocks VKOR and creates vitamin K deficiency
calcium & phospholipids are required for
tenase & prothrominase complexes to form
tissue factor aka
factor III
how long does it take blood to clot in a glass tube?
4-8 minutes
prothrombin time (PT)
assess extrinsic pathway (12-14 sec)
monitor warfarin
activated partial thromboplastin time (aPTT)
assess intrinsic pathway (26-33sec)
monitor heparin
prolongation of PT & aPTT indicates defect in
common pathway
hemophilia A
deficiency of factor VIII
hemophilia B
deficiency in factor IX
hemophilia C
deficiency in factor XI