Platelets Flashcards

1
Q

what is haemostasis?

A

the stoppage of bleeding

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2
Q

what features of the epithelium prevents adhesion?

A

nitric oxide and prostaglandins are secreted and collagen covered

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3
Q

what do smooth muscle cells do in the epithelium?

A

allow contraction and relaxation

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4
Q

what do alpha granules do?

A

contain adhesive proteins that cause a glue-like effect

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5
Q

what do dense granules do?

A

contain activators which activate other platelets

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6
Q

what does the vWF receptor bind to?

A

glycoprotein 1b59

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7
Q

what does collagen bind to?

A

alpha 2 beta 1 and glycoprotein 6

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8
Q

what does alpha II beta III bind to?

A

fibrinogen

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9
Q

how does tethering occur?

A

vWF binds to glycoprotein 1b59 causing a velcro effect

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10
Q

what is activation?

A

platelet releases granule contents, which opens up adhesion receptor

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11
Q

what binding occurs in activation?

A

collagen binding to glycoprotein 6

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12
Q

what is adhesion?

A

single layer of platelets bind to the exposed ECM

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13
Q

what binding occurs in adhesion?

A

collagen binding to alpha 2 beta 1

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14
Q

what happens in secretion?

A

platelet releases ADP and TxA2 which bind to their receptors

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15
Q

what is aggregation?

A

multiple layers of platelets bind to each other

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16
Q

what binding occurs in aggregation?

A

fibrinogen binds to alpha 2 beta 3

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17
Q

what does tirofiban do?

A

targets alpha 2 beta 3 so no aggregation

18
Q

what does aspirin and clopidogrel do?

A

inhibit activation of platelets so cannot form a clot

19
Q

what is bernard-souilier syndrome?

A

abnormality in glycoprotein 1b59 so collagen cannot bind

20
Q

what is glanzmann disease?

A

abnormality in the genes for alpha 2 beta 3

21
Q

what are the symptoms of platelet associated disease?

A

easy bruising, menstrual bleeding heavy, abdormal bleeding after surgery

22
Q

what are storage pool deficiencies?

A

caused by a lack of granules or their content or inability to empty them

23
Q

what is grey platelet syndrome?

A

lack of alpha granules and their contents

24
Q

what is zymogen?

A

inactive substance that is activated by enzymes

25
Q

what is the purpose of coagulation?

A

helps form an insoluble mesh to help strengthen the clot

26
Q

what is the key process of coagulation?

A

activation of thrombin

27
Q

what does thrombin do?

A

converts fibrinogen to fibrin

28
Q

how does initiation of coagulation begin?

A

tissue factor coming into contact with the blood

29
Q

what does the tissue factor bind to?

A

factor 7 which becomes factor 7a

30
Q

what does the binding of tissue factors cause?

A

the activation of F9 and F10

31
Q

what does activation of F9 and F10 do?

A

switches on thrombin to convert the fibrinogen to fibrin

32
Q

what does thrombin do once activated?

A

activates F5 and F8, which further activates F9 and F10

33
Q

what does tissue plasminogen activator do?

A

released into the blood to allow the clot formation to be controlled

34
Q

what is plasminogen?

A

an inhibitor that dissolves the blood clot

35
Q

what is the extrinsic pathway?

A

rapid pathway activated by external trauma that causes blood to escape

36
Q

what is the intrinsic pathway?

A

more complex, activated by inside trauma such as when collagen exposed

37
Q

what types of haemophilia are sex linked?

A

A and B

38
Q

what are the symptoms?

A

nose bleeds, brusing, gum bleeds, purpura and petechiae

39
Q

how can you test for haemophilia?

A

coagulation screening

40
Q

what is a prothrombin time test?

A

adds thromboplastin to activate factor 7 for the extrinsic pathway

41
Q

what is an activated partial thromboplastin time test?

A

activates the intrinsic pathway

42
Q

what happens if both of these tests are slow?

A

shows a defect in the common pathway