Bleeding And Thrombosis Flashcards

(17 cards)

1
Q

Humoral mediators in plasma

A

Epinephrine
Thrombin

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2
Q

Mediators released from activated platelets

A

adenosine diphosphate, serotonin

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3
Q

and vessel wall
extracellular matrix constituents that come in contact with adherent
platelets

A

Collagen, vWF

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4
Q

most
abundant receptor on the platelet surface.

A

Gp) IIb/IIIa (αIIbβ3

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5
Q

We now know that coagulation is normally initiated through
tissue factor (TF) exposure and activation through

A

the classic extrinsic
pathway but with critically important amplification through elements
of the classic intrinsic pathway,

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6
Q

TF is constitutively expressed on the surfaces
of

A

subendothelial cellular components of the vessel wall, such as
smooth muscle cells and fibroblasts.

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7
Q

pivotal protease of the
coagulation system.

A

Thrombin

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8
Q

multifunctional
enzyme that converts soluble plasma fibrinogen to an insoluble fibrin matrix

A

Thrombin

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9
Q

covalently cross-links
and thereby stabilizes the fibrin clot.

A

Factor 13a

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10
Q

acts as an anticoagulant by cleaving and inactivating activated factors
V and VIII.

A

Activated protein C, accelerated by a cofactor, protein S,

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11
Q

cleaves the N-terminal lysine residues
of fibrin, which aid in localization of plasmin activity

A

thrombin-activatable fibrinolysis inhibitor (TAFI

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12
Q

primary inhibitor
of tPA and uPA in plasma.

A

plasminogen activator inhibitors (PAI-1)

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13
Q

main inhibitor of plasmin in human plasma, inactivating any
nonfibrin clot–associated plasmin.

A

α2-antiplasmin

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14
Q

inhibit platelet binding, secretion, and
aggregation.

A

antithrombotic
effects. They produce prostacyclin, nitric
oxide, and ectoADPase/CD39,

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15
Q

activate
fibrinolytic mechanisms through the pro-
duction of tissue plasminogen activator,
urokinase, plasminogen activator inhibi-
tors, and annexin-2.

A

anticoagulant factors including hepa-
ran proteoglycans, TF pathway inhibitor,
and thrombomodulin.

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16
Q

neutralizes
thrombin and other activated coagulation factors by forming a com-
plex between the active site of the enzyme and its reactive center

17
Q

hallmark of moderate and severe factor VIII and
IX deficiency and, in rare circumstances, of other clotting factor
deficiencies

A

Spontaneous
hemarthroses