Test 2 - Clotting Flashcards

1
Q

Three phases of hemostasis

A

formation of a platelet plug, coagulation, fibrinolysis

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2
Q

Formation of a plug (3)

A

Platelet: adhesion, activation, aggregation

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3
Q

Vwf

A

protects coag factor 8

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4
Q

Vwf binding site

A

Glycoprotein 1b

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5
Q

What makes Vwf bind to platelets?

A

change in shear rate

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6
Q

vWF coagulation via

A

glycoprotein VI receptor and A2B1 integrin

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7
Q

most common congenital bleeding disorder

A

vWF

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8
Q

Treatment of vWF

A

DDAVP or other clotting shit we use

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9
Q

Platelet activation at site

A

activated by agonists - collagen, thrombin, ADP, epinepherine

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10
Q

Platelet activation basics

A

change in morphology, release contents of alpha grannules - ADP, serotinin, factor V, factor VIII, vWF, Fibrinogen

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11
Q

What signals from the damaged site?

A

collagen and vWF

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12
Q

After binding (basics) what happens?

A

they undergo degranulation * release cytoplasmic granules (seratonin, adp, thromboxane A2)

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13
Q

Serotonin function

A

vasoconstrictor

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14
Q

ADP signals

A

more platelets to the area

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15
Q

Thromboxin promotes

A

platelet aggregation & degranulation & vasoconstriction

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16
Q

When platelets keep sticking what happens?

A

Thromboxane and ADP keep signaling even MORE platelets.

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17
Q

^ this forms

A

a platelet plug

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18
Q

1st factor damage tissue releases

A

factor III

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19
Q

Factor III + Ca =

A

Factor 7, initiating the extrinsic mechanism

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20
Q

Facor XII from activated platelets or collagen

A

(12 )to 11 to 9+8 , initiating the intrinsic mechanism

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21
Q

Factor 7 from extrinsic and 9 from intrinsic form

A

factor X

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22
Q

Factor X + 3 + V + Ca + PF3 activates

A

prothrombin activator

23
Q

prothrombin activator activates

A

prothrombin to thrombin

24
Q

Thrombin converts

A

fibrinogen to fibrin

25
Fibrin forms
a loose mesh on platelet patch
26
Which factor forms cross links on fibrin?
13. forms stabilized fibrin13
27
What gets caught in this mesh?
more platelets and blood cells
28
Apsrin inhibits
synthesis of thromboxin a2
29
Thromboxin function
platelets to change shape, release granules, aggregate
30
Heparin binds to
anti-thrombin, creating a conformational change, ^ inactivation properties (from slow to rapid)
31
Heparin-antithrombin complex inhibits
factor 7a (tissue factor) 9a, 10a 2a (happen to be the calcium and K factors)
32
zymogen
pro-enzyme
33
Vit K factors
9 10 7 2 (7 + 2 = 9, 0K?) 0k (zero k)
34
vitamin k function
catalyzes carboxylation of glutamic acid which metabolizes to gamma-carboxyglutamic acid. deters factors from binding to Ca, thus inhibiting their activation
35
Purpose of vitamin K
makes it possible for the factor to bind to calcium
36
Coumadin inhibits carboxylation of vit k factors
prevents ca from binding. Renders them inert
37
hemophilia a
defect of f8
38
hemophilia b
def of 9
39
Hemostatic actions of thrombin
clevage fibrinogen to fibrin. Activates 13 to cross link fibrin, activates platelets, activates V VII VIII IX, activates fribrinollysis inhibitor, stim production of TF(f7)and vWF. Stims subendothelial smooth muscle constriction
40
coagulation initiation factors
x via 7, 9 via 7
41
coagulation amplification factors
2a 11a
42
propagation
9a 10a via 2a
43
regulation of coagulation (3)
TFPI, AT, PC
44
TFPI
Tissue factor pathway inhibitor, inhibits 7, 7&10 complex
45
AT
atithrombin inhibits 10a and thrombin
46
PC
Protein C inhibits Fva and FV8
47
How Heparin works
binds to AT and shifts it from a slow to rapid inhibitor of thrombin
48
Neonates have low levels of both…
procoagulant and anticoagulant
49
neonates have a well balanced
hemostatic system
50
Neonate platelet counts = __% adult values
100
51
contents of platelet dense granules
50% of adult
52
fetal form of fibrinogen
less dense
53
plasminogen of neonates ___ adult value
50%