BLOOD 5 Flashcards

(28 cards)

1
Q

What are platelets needed for?
What does thrombopoietin do?
Platelet half-life

A

Blood clotting
Increases platelet numbers
10 days

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2
Q

Three phases of hemostasis

A

1) Vascular phase
2) Platelet phase
3) Coagulation phase

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3
Q

Vascular phase

Vasoconstriction prolonged by?

A

Neurogenic and myogenic control

Serotonin, Endothelin-1, Thromoboxane A2

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4
Q

Platelet phase

A

1) Exposed collagen: binds and activated platelets
2) Factors released from platelet
3) Factors attract more platelets
4) Platelets aggregate from plug

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5
Q

Platelet Phase?
Where the von Willebrand factor made?
What does it bind to?
What effect does it have?

A

Endothelial cells and platelets
Binds to both collagen and platelets
Causes aggregation of platelets

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6
Q

Factors that cause platelet aggregation

A

ADP
paf
Serotonin
Thromboxane a2

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7
Q

What does platelet aggregation lead to

A

Vasoconstriction

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8
Q

Platelet activation

A

Helps adhesion

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9
Q

What the role of Prostacyclin (prostagladin I2, PG12 and nitiric oxide (NO).

A

Prevent platelet adhesion and are vasodilators

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10
Q

What is prostacyclin

A

anti-coagulant

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11
Q

Arachidonic acid leads to PGH2 synthesis: produces three chemicals?

A

1) Prostaglandins
2) Thromboxane A2
3) Prostacyclin

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12
Q

Cyclooxygenase?

Aspirin?

A

Causes synthesis

Inhibits thromboxane A2

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13
Q

Coagulation cascade common pathway:

1) Factor X
2) Prothrombin
3) Fibrinogen
4) Factor XIII

A

1) Active X
2) Thrombin
3) Fibrin
4) Active XIII

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14
Q

What is the final product of the coagulation cascade?

What cofactor is required for blood clotting?

A

Cross-linked fibrin polymer

Ca+

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15
Q

Where is the Extrinsic Pathway found
Responds to ?
Name the 4 tissue factors involved?
Which factor causes (+) feedback

A

Found in tissues
Cell injury
Factor VII, Factor III, Factor IX and X
Active factor X

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16
Q

What Intrinsic pathway respond to?
Which factors are activated?
Factor XI is activated by?

A

Contant activation
Factors: XII, XI, IX
Thrombin positive feedback from common pathway of thrombin

17
Q

Which factor does the von willebrand factor regulate
Why is vitamin K required?
What is Cuomadin (Warfarin) and what its function?

A

Levels of VIIII
Synthesis of thrombin, VII, IX and X
Anticoagulant which blocks the action of vitamin K

18
Q

One effect of a deficiency in factor IX and factor VIII?

A

Severe bleeding

19
Q

Cell based: location
Initiation phase
What starts this phase?

A

Cell membrane of smooth muscle?

Exposure of tissue factor: starts to produce small amounts of thrombin

20
Q

Amplification phase

Which factors does thrombin activate?

A

Factors V, XI and VIII

21
Q

Propagation phase
Active factors on the surface of platelets form ?
What is a thrombin burst?

A

Tenase

When prothrombin cleaves large amount of prothrombinase result in large amounts of thrombin

22
Q

Three characteristics of von Willebrand disease

A

1) Most common coagulation disorder
2) Problems in quality or quanitity of von willebrand factor
3) Areas with high number of smlal capillaries (skin, gi tract, uterus)

23
Q

Causes of Hemophilia A

Causes of Hemophilia B

A

Factor VIII

Factor IX

24
Q

How is the clot removed after healing has taken place?

What is this process called?

A

Requires thrombin, plasminogen and tPA to form plasmin: which cleaves the fibrin polymer to firbin fragments
Firbinolysis

25
Where is tPA released? Thrombus? Embolus?
Slowly by the endothelium Blood clot attached to vessel wall Floating blood clot
26
Physiological anticoagulants: released from: 1) Plasminogen/Plasmin 2) Tissues plasminogen activator (tPA) 3) Antithrombin III 4) Prostacyclin
1) Liver 2) Mant tissues 3) Liver 4) Endothelial cells
27
Physiological anticoagulants: activated by: 1) Plasminogen/Plasmin 2) Tissues plasminogen activator (tPA) 3) Antithrombin III 4) Prostacyclin
1) tPA and thrombin 2) Normally present 3) Heparin 4) N/A
28
Physiological anticoagulants function: 1) Plasminogen/Plasmin 2) Tissues plasminogen activator (tPA) 3) Antithrombin III 4) Prostacyclin
1) Breaksdown fibrin 2) Activates plasminogen 3) Blocks IX,X, XI,XIII, thrombin 4) Inhibits platelet aggregation