3rd semester 2nd MT Flashcards

1
Q

Which protease are responsible for the destruction of the intrinsic tenase and the prothrombinase complexes?

A

Thrombin

Protein C

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2
Q

Which protein co factors are responsible for the destruction of the intrinsic tenase and the prothrombinase complexes?

A

Thrombomodulin

Pritein S

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3
Q

Throughput of K+ ch

A

1-2x10^8

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4
Q

What carries the most info on the memb. Topology of an ion ch?

A

Hydropathy plot

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5
Q

Streptokinase mechanism

A

Human plasminogen in a complex with streptokinase becomes a plasminogen activator

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6
Q

What is the mode of antifibrinolytic action of TAFIa?

A

Cleaves C terminal Lys residues -> decreases the binding site for the tPA and plasminogen in fibrin and moderates the cofactor function of fibrin in plasminogen activation

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7
Q

Coumarin effect, in what drug is it present?

A

Warfarin

Decreases blood clotting by blocking an enzyme called vitamin K epoxide reductase that reactivates vitamin K

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8
Q

When do Ca ch. permits Na entrance?

A

When Ca conc is decreased

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9
Q

How does thrombin activates platelets?

A

Hydrolysis of memb. Proteins

Increasing cytosolic Ca conc.

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10
Q

tPA job?

A

Protein involved in the breakdown of blood clots

Catalyzes plasminogen -> plasmin

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11
Q

K+ ch structure

A

Tetramer

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12
Q

What stabilizes fVIII?

A

vWf

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13
Q

What is the role of TXA2 and what cell produces it?

A

Pro thrombotic effect

Produced by activated platelets

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14
Q

Structure of ATP sens. K+ ch

A

Octamer
4 kir6.2
4 SUR

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15
Q

Thrombaxane is inhibited by

A

Aspirin

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16
Q

NO will lead to?

A

Vasodilation

Increased blood flow

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17
Q

2 functions of vWf?

A

Carrier of fVIII

Mediator of platelet adhesion at high shear

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18
Q

Synthesis of NO starts from?

A

Arg

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19
Q

What activates protein C?

A

Thrombomodulin bound thrombin

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20
Q

What is the mode of activation of streptokinase?

A

Forms a complex with human plasminogen in which plasminogen gains activity as plasminogen activator

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21
Q

How does thrombomodulin modify blood coagulation?

A

Accelerates protein C activation by thrombin

22
Q

What stimulates tPA?

23
Q

Hemophilia B is caused by deficiency in?

24
Q

Anti-phospholipid syndrome can be treated with (2)

A

Vit K antagonist

Heparin

25
What is the background of activated protein C resistance?
Arg 506 in fV is mutated
26
What can be a substrate for thrombin?
``` Fibrinogen V VIII XI XIII Platelets ```
27
Because_________ is inhibited by Aspirin, there is no production of _______ and _________
COX TXA2 PGI2
28
What will deficiency in vit K leads to?
Reduces protein C levels | Reduces prothrombin levels
29
Actions of Heparin?
Facilitates thrombin inactivation by antithrombin
30
Where is the pore loop located?
Extracellularly
31
Effect of Sulfonylurea on ATP sensitive K channels, where do they bind?
Inhibit the ch -> depol -> insulin secretion | Binds SUR1
32
Ion ch are stochastic or deterministic?
Stochastic
33
How is fibrinolysis terminate?
a2 plasmin inhibitor inactivates plasmin
34
How can tPA activity increase?
In the presence of fibrin
35
List 3 plasminogen activators used in therapy?
tPA uPA Streptokinase
36
3 phases of platelets activation:
1. Adhesion 2. Activation 3. Aggregation
37
Antithrombotic effects of thrombin?
Thrombin-TM complex activates protein C which will inhibit fV and fVIII
38
Substrates for factor VIIa?
fX | fIX
39
Structural consequence of coumarine?
Inhibition of Gla domain formation
40
ecto ATPase activity?
Inhibition of platelets activation
41
What are the vit K dependent factors?
II VII IX X
42
What is TAFI (Thrombin Activatable Fibrinolysis Inhibitor)
Carboxypeptidase
43
What activates TAFI?
Thrombin-TM complex
44
TAFI action?
Reduces fibrinolysis by removing the C terminal residues that are important for the binding and activation of plasmin
45
hirudin action?
inhibits thrombin directly
46
how can the activity of tPA be increased?
in the presence of fibrin
47
location of CFRT?
apical side of endothelial cells
48
describe each hemophilia A B C
A- fVIII B- fIX C- XI
49
what is the most frequent cause of hemophilia?
Antiphospholipid syndrome
50
where can we find Gla-domain?
``` II VII IX X protein C, Z, S ```
51
when will we give hirudin?
when a persim lacks antithrombin
52
what factor inhibits plasmin and how?
fXIIIa | makes Gln-Lys isopeptide bonds btw a2-antiplasmin and plasmin