BL- COAG 2 Flashcards

1
Q

Antithrombin: A serpin

A

serine protease inhibitor

inhibits coagulation

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2
Q

Does antithrombin only inhibit thrombin?

A

NO

2a and 10a also

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3
Q

A highly sulfated glycosaminoglycan

A commonly used anticoagulant

Acts as a cofactor for antithrombin

A

Heparin

Heparan sulfate, a related compound, produced by endothelial cells (masts and basos)

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4
Q

Another Vitamin K-dependent serine protease

Activated by thrombin

Inactivates Factor Va and Factor VIIIa

Protein S is a cofactor

A

Protein C

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5
Q

Factor V Leiden: A mutation of factor V that makes it resistant to ________ by protein C

A

inactivation

*“APC resistance.”

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6
Q

a small protein molecule that inactivates several enzymes of the coagulation system.

A

Antithrombin

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7
Q

Protein C inactivates

A

Factor Va and Factor VIIIa

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8
Q

performs these operations primarily by proteolytically inactivating proteins Factor Va and Factor VIIIa.

A

Protein C

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9
Q

Common risk factor for venous thromboembolism

A

Factor V Leiden

A mutation of factor V
*“APC resistance.”

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10
Q

A proteinase inhibitor
Constitutively expressed by endothelial cells

Inhibits extrinsic tenase by binding and inactivating the complex

A

Tissue Factor Pathway Inhibitor (TFPI)

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11
Q

Anticoagulation mechanisms

A
  • Antithrombin
  • Tissue Factor Pathway Inhibitor (TFPI)
  • Factor V Leiden
  • Protein C
  • Heparin
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12
Q

genetically inherited disorder of blood clotting. ___________ is a variant of human factor V that causes an increase in blood clotting (hypercoagulability)

A

Factor V Leiden

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13
Q

a single-chain polypeptide which can reversibly inhibit Factor Xa (Xa).

A

Tissue Factor Pathway Inhibitor (TFPI)

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14
Q

a process that prevents blood clots from growing and becoming problematic.[1] This process has two types

A

Fibrinolysis- Key enzyme: Plasmin

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15
Q

Plasmin

A

Derived from plasminogen through cleavage by tissue plasminogen activator (t-PA) or urokinase (u-PA)

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16
Q

Plasminogen Activator Inhibitor-1 (PAI-1)

A

Binds to t-PA and u-PA and inactivates them

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17
Q

an important enzyme present in blood that degrades many blood plasma proteins, including fibrin clots.

A

Plasmin

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18
Q

serpin that functions as the principal inhibitor of tissue plasminogen activator (tPA) and urokinase (uPA), the activators of plasminogen and hence fibrinolysis (the physiological breakdown of blood clots).

A

Plasminogen Activator Inhibitor-1 (PAI-1)

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19
Q

important fibrin degreadation products

A

D Dimer

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20
Q

Inhibition of Fibrinolysis

A

Plasminogen Activator Inhibitor-1 (PAI-1)

a2- antiplasmin

thrombin- activatable fibrinolysis inhibitor

21
Q

a serine protease inhibitor (serpin) responsible for inactivating plasmin, an important enzyme that participates in fibrinolysis and degradation of various other proteins.

A

Alpha 2-antiplasmin

22
Q

An exopeptidase involved in Inhibition of Fibrinolysis

A

Thrombin-Activatable Fibrinolysis Inhibitor (TAFI)

23
Q

a fibrin degradation product (or FDP), a small protein fragment present in the blood after a blood clot is degraded by fibrinolysis.

24
Q

α2-Antiplasmin

A

Another serpin

Binds to plasmin and inactivates it

25
____ is used in some cases of diseases that feature blood clots, such as pulmonary embolism, myocardial infarction, and stroke, in a medical treatment called thrombolysis
Therapeutic tPA
26
In resting state, _______tends to prevent clotting
Endothelium
27
Produces heparan sulfate
Endothelium Resting state
28
Endothelium Exposure of tissue factor
With vessel damage, promotes clot formation
29
Expresses thrombomodulin → protein C activation
Endothelium Resting state
30
With vessel damage, _______promotes clot formation
Endothelium
31
Release of von Willebrand factor from Weibel-Palade bodies of the endothelial cells
With vessel damage, endothilum promotes clot formation
32
Expresses TFPI
Endothelium Resting state
33
von Willebrand factor
a blood glycoprotein involved in hemostasis primary function is binding to other proteins, in particular factor VIII, and it is important in platelet adhesion to wound sites
34
Exposure of subendothelium, leading to platelet adhesion and activation
With vessel damage, endothilum promotes clot formation
35
Binds to subendothelium via collagen, von Willebrand factor, and other proteins
Role of the platelet
36
Forms a platelet plug at the site of injury
Role of the platelet
37
Synthesizes t-PA and u-PA
Endothelium Resting state
38
Release of substances that cause vasoconstriction
With vessel damage, endothilum promotes clot formation
39
With activation, exposes anionic phospholipids that act as a surface for coagulation to take place
Role of the platelet
40
Synthesizes PGI2 (prostacyclin) and nitric oxide → vasodilitation
Endothelium Resting state
41
Releases multiple substrates for coagulation
Role of the platelet
42
Metabolizes ADP (platelet agonist) to AMP + adenosine (platelet inhibitor)
Endothelium Resting state
43
a blood glycoprotein involved in hemostasis primary function is binding to other proteins, in particular factor VIII, and it is important in platelet adhesion to wound sites
Von Willebrand factor's
44
is Von Willebrand factor's an enzyme?
No- It is NOT an enzyme and, thus, has no catalytic activity.
45
dRVVT
``` good if prolonged aPTT activates factor 10 if SLE (antiphoslipid) this test wont change ```
46
APS | Antiphospholipid SLE
must ave positive AB panal 6 weeks apart in setting of miscarriage or thrombosis
47
Labs for DIC
``` Fibrinogen D-Dimer CBC PT aPTT ```
48
How do you ALWAYS treat DIC
Treat the underlying disorder
49
``` Prolonged PT Greatly prolonged PTT Prolonged thrombin time Low platelet count Low fibrinogen level Increased fibrin split products Increased D-dimer ```
Labs for DIC