18/19 - Hemostasis and Thrombosis Review Flashcards

1
Q

components for platelet activation

A

glycoprtn 1b binds to vWF

other glycoprtns bind to collagen to activate platelets

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2
Q

activated platelets secrete

A

ADP
TXA2
5-Ht

these bind to platelets and activate GP IIb/IIIa

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3
Q

activated GP IIb/IIIa binds…

A

to fibrinogen

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4
Q

______ cleaves fibrinogen into fibrin

A

thrombin

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5
Q

thrombin further activates platelets b binding to and activating the _________

A

protease activated receptor PAR

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6
Q

how does thrombomodulin work in the anticoagulation system?

A

thrombomodulin pairs with thrombin on a receptor on endothelial cells that activates prtn C to APC which activates prtn S whcih inhibits VIIIa and Va to stop the formation of thrombin

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7
Q

what does antithrombin do?

A

inactivates thrombin and factor Xa

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8
Q

what is the role of heparin sulfate?

A

binds antithrombin and significantly increases rate of thrombin and factor Xa inactivation

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9
Q

where is fibrinogen converted into fibrin?

A

active site of thrombin

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10
Q

does the antithrombin/heparin sulfate complex inhibit thrombin bound to fibrin?

A

NO

therefore thrombin is not inactivated at the site of the clot

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11
Q

inappropriate clot formation

A

thrombosis

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12
Q

“platelet poor” thrombosis aka “red thrombosis”

A

venous thromboisis

antiplatelet therapies will not be useful

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13
Q

“white thrombosis”

A

arterial thrombosis

antiplatelet therapy useful

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14
Q

most common cause of MI and ischemic strokes

A

arterial thrombosis

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15
Q

factor V leiden mutation

A

decreased control of thrombin generation (more)

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