What is hemostasis?
Cessation of blood loss from a damaged vessel
Hemostasis occurs in 4 phases, what are they?
Following injury to the vessel wall, the initial event is what?
Vasoconstriction
–which is a transient, locally induced phenomenon
Platelets, in healthy endothelium, remain in their unactivated state. What mediators are released in order to inhibit platelet aggregation?
Chemical mediators
Blood vessel injury exposes what?
Exposes:
–collagen, Von Willebrand factor (vWF): these are components of the extra cellular matrix
The platelet plasma membrane contains what collagen receptors?
GPVI and vWF receptors (GPIb)
–binding of the collagen and vWF on the extra cellular matrix to these receptors causes the platelet to adhere to the subendothelium
Binding of the collagen and vWF to the platelet results in platelet activation, leading to the release of the contents of the cells’ granules:?
ADP, Ca2+, ATP, serotonin, vWF, and platelet factor 4
–all secreted from platelet granules
What is the action of ADP?
Mediates platelet aggregation
Activated platelets synthesize and release what?
Thromboxane A2 (TXA2)
Activation of platelets is enhanced by the generation of thrombin through the coagulation cascade; thrombin is an important platelet agonist. Thrombin receptors are what?
Protease activated G protein coupled receptors
—activation of thrombin receptors results in activation of PLC and inhibition of adenylyl cyclase
Signaling molecules released by activated platelets activate receptors on the plasma membrane of resting platelets circulating nearby. What happens next in the cascade?
Previously dormant platelets become activated and start to aggregate
Platelet aggregation is mediated primarily by what?
Fibrinogen
–soluble plasma glycoprotein
Binds simultaneously to GPIIB/IIIa receptors on two separate platelets
–this leads to platelet cross linking and platelet aggregation which leads to clot formation
GPIIb/IIIa does not bind fibrinogen on nonstimulated platelets
Platelet activation converts GPIIb/IIIa from a low affinity fibrinogen receptor to a high affinity receptor
The above cards went through the formation of a platelet plus (primary hemostasis). Now secondary hemostasis is the coagulation cascade. How does blood start to coagulate after primary hemostasis?
Transformation of soluble fibrinogen into insoluble fibrin
Thrombin does what?
Catalyzes the conversion of fibrinogen to fibrin
–which is incorporated into the plug
–this is the last step of the coagulation cascade
Cross-linking of the fibrin strands stabilize the clot and forms the hemostatic plug
The coagulation cascade is a sequence of enzymatic events. The coagulation factors are generally serine proteases. Most plasma coagulation factors circulate as inactive proenzymes, which are synthesized by the liver. These proenzymes are proteolytically cleaved, and thereby activated, by the activated factors that precede them in the cascade
:)
There are two pathways of the coagulation pathway. Describe the intrinsic pathway first
Activated in vitro by factor XII (Hageman factor)
Describe the extrinsic pathway
In vivo is initiated by activation of clotting factor VII by the tissue factor (Thromboplastin)
Both the intrinsic and extrinsic coagulation pathways lead to the activation of what?
Factor X.
Moving on to Vitamin K, what is the action of this vitamin?
Blood clotting factors II, VII,IX and X
–must undergo a vitamin K dependent post translational modification, which involves the gamma carboxylation of a number of glutamic acid residues
Vitamin K is regenerated from the epoxide by what?
Vitamin K epoxide reductase
Finally after vascular injury, anticoagulant factors are secreted by the endothelium:
Prostacyclin (PGI2) Antithrombin III Proteins C and S Tissue Factor Pathway Inhibitor (TFPI) Tissue Type Plasminogen Activation (t-PA)
How does PGI2 work as an anticoagulant factor?
Increases cAMP levels within platelets
–inhibit platelet activation
Also a vasodilator
–increases cAMP levels in the vascular smooth muscle cells
How does antithrombin III work as an anticoagulant factor?
Inactivates thrombin and other coagulation factors
–by forming a complex with them
How does protein C and S work as a anticoagulant agents?
Protein C
–vitamin K dependent serine protease that is activated by thrombin
Protein C and S
–degrade factors Va and VIIIa