BLOOD 2 Flashcards

1
Q

ASPRIN what do mem phospholipids give rise to

A

arachidonic acid

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2
Q

ASPRIN under influence of COX1 what can arachidonic acid be converted into

A

TXA2

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3
Q

ASPRIN where is COX 1 located

A

platelets

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4
Q

ASPRIN what is the function of TXA2

A
  1. vasoconstriction

2. increase platelet aggregation

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5
Q

ASPRIN what kind of substance is TXA 2

A

pro-hemostatic

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6
Q

ASPRIN under influence of COX2 what can arachidonic acid be converted into

A

prostacyclin

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7
Q

ASPRIN where is COX 2 located

A

endothelium

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8
Q

ASPRIN what is the function of prostacyclin

A
  1. vasodilation

2. decrease platelet aggregation

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9
Q

ASPRIN what kind of substance is prostacyclin

A

anti-hemostatic

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10
Q

ASPRIN what is the function of aspirin

A

inhibit COX 1 and COX 2

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11
Q

ASPRIN what does aspirin have stronger effect on

A

COX 1

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12
Q

ASPRIN what is net effect of aspirin

A

anti hemostatic

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13
Q

BLOOD CLOT what is blood clot

A

blood cells trapped in network of fibrin proteins

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14
Q

BLOOD CLOT why can’t fibrin be present all the time

A

it will cause blood blot

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15
Q

BLOOD CLOT what is precursor for fibrin

A

soluble plasma protein fibrinogen

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16
Q

BLOOD CLOT what is the function of active thrombin

A

convert fibrinogen to fibrin

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17
Q

BLOOD CLOT why can’t thrombin be present all the time

A

it will cause fibrin to form

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18
Q

BLOOD CLOT what is precursor of thrombin

A

inactive enzyme prothrombin

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19
Q

BLOOD CLOT what is the function of prothrombinase

A

convert prothrombin to thrombin

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20
Q

BLOOD CLOT what is the function of factor 13a and Ca++

A

convert unstable fibrin to stable fibrin

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21
Q

BLOOD CLOT what is prothrombinase

A
  1. factor 5a
  2. factor 10a
  3. Ca++
  4. phospholipids
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22
Q

BLOOD CLOT what pathways are involved in activating factor 10a (traditional)

A

1, intrinsic

2. extrinsic

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23
Q

BLOOD CLOT what imitates intrinsic pathway

A
  • blood comes into contact w something foreign

- nothing needs to be added to blood

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24
Q

BLOOD CLOT what is intrinsic pathway

A
  1. contact activation converts factor 12 to active form
  2. active factor 12 converts factor 11 to active form
  3. active factor 11 converts factor 9 to active from (in presence of Ca++)
  4. active factor 9 forms tenasec complex w factor 8, Ca++, and PL
  5. tenase complex converts factor 10 to active form
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25
BLOOD CLOT what initiates extrinsic
tissue damage
26
BLOOD CLOT why does tissue damage initiate extrinsic pathway
adds tissue factor to blood
27
BLOOD CLOT what happens when extrinsic pathway initated
1. TF added to blood 2. TF forms complex with factor 7a, Ca++. and PL 2. complex converts factor 10 to active form
28
BLOOD CLOT what happens when there is deficiency in factor 12
- in vivo there is clotting | - in vitro there is no clotting
29
BLOOD CLOT what is box in top left hand corner labelled
- intrinsic (traditional) | - amplification (physiological)
30
BLOOD CLOT what is box in top right hand corner labelled
- extrinsic (traditional) | - invitation (physiological)
31
BLOOD CLOT what pathway stayed same for tractional and physiological blood clotting
common pathway
32
BLOOD CLOT PHYSIOLOGICAL what pathways are involved in activating factor 10a (physiological)
1. amplification pathway | 2. initiation pathway
33
BLOOD CLOT PHYSIOLOGICAL what are steps of initiation pathway
1. TF added to blood 2. Tf forms complex w factor 7a. Ca++, and PL 3. complex converts factor 10a to active form
34
BLOOD CLOT PHYSIOLOGICAL what was discovered about complex that forms during initiation pathway
responsible for activating factor 9
35
BLOOD CLOT PHYSIOLOGICAL what happens when factor 9 activated
active factor 9 forms tenase complex with active factor 8, Ca++, and PL 2. tenase complex converts factor 10 to active form
36
BLOOD CLOT PHYSIOLOGICAL what are 2 ways of activating factor 10 in physiological
1. through TF complex directly | 2. through TF complex indirectly by activating factor 9
37
BLOOD CLOT PHYSIOLOGICAL what happens in amplification pathway
1. factor 11 converted to active form 2. active factor 11 converts factor 9 to active from (in presence of Ca) 3. active factor 9 forms tenase complex with active factor 8, Ca++, and PL 4 tenase complex converts factor 10 to active form
38
BLOOD CLOT PHYSIOLOGICAL how can active factor 9 be obtained
1. initiation pathway | 2. amplification pathway
39
BLOOD CLOT PHYSIOLOGICAL what function of thrombin was discovered
1. activates factor 13 2. activates factor 5 (prothrombinase) 3. activates factor 8 (tenase) 4. activates factor 11
40
BLOOD CLOT PHYSIOLOGICAL when does prothrombinase and tenase complex work better
in presence of thrombin
41
BLOOD CLOT PHYSIOLOGICAL what happens in blood clotting
1. tissue damage 2. small amount of TF for small amount of factor 10 a 3. small amount of factor 10a for small amount of prothrombinase 4. small amount of ptothrombinase for small amount of thrombin 5. small amount of thrombin for small amount of fibrin 6. thrombin feed back to cause amplification
42
REGULATION OF BLOOD CLOT what is fibrinolysis
break down of fibrin by fibrinolytic system
43
REGULATION OF BLOOD CLOT what are natural anti coagulants
1. tissue factor pathway inhibitor | 2. antithrombin 3
44
REGULATION OF BLOOD CLOT what is the function of tissue factor pathway inhibitor
1. inhibit factor 10a | 2. inhibit factor 7a
45
REGULATION OF BLOOD CLOT what is the function of antithrombin 3
inhibit thrombin
46
REGULATION OF BLOOD CLOT when can thrombin have anti coagulant activity
when it binds to thrombo modulin
47
REGULATION OF BLOOD CLOT what is the function of thrombin + thrombomodulin complex
1. activate protein C 2. break down factor 5a (part of prothrombinase complex) 3. breakdown factor 8a (part of tenase complex)
48
REGULATION OF BLOOD CLOT what are clinical anti coagulants
1. Ca chelators 2. heparin 3. agonists of vitk
49
REGULATION OF BLOOD CLOT what is the function of Ca chelators
remove Ca++
50
REGULATION OF BLOOD CLOT what is the function of heparin
increase activity of antithrombin 3
51
REGULATION OF BLOOD CLOT what is the function of agonists of vitk
inhibits synthesis of facotrs that require vit K
52
REGULATION OF BLOOD CLOT what are factors that require vit K to be synthesized
2,7,9,10
53
FIBRINOLYSIS in fibrinolysis what can fibrin get broken down to
fibrin degradation products (FDP)
54
FIBRINOLYSIS what causes fibrinolysis
enzyme plasmin
55
FIBRINOLYSIS why is plasmin not present in active form all the time
don't want it break down clots before tissue is done healing
56
FIBRINOLYSIS what is inactive form of plasmin
plasminogen
57
FIBRINOLYSIS when does plasminogen get converted to plasmin
in presence of plasminogen activators
58
FIBRINOLYSIS what are 2 categories of plasminogen activators
1. natural | 2. clinical
59
FIBRINOLYSIS what are natural plasminogen activators
1. tissue plasminogen activator | 2. exercise
60
FIBRINOLYSIS what is a clinical plasminogen activator
tenectaplase
61
ABNORMAL HEMOSTASIS what is abnormal hemostasis
change in balance bw pro-hemostatic factors and anti-hemostatic factors
62
ABNORMAL HEMOSTASIS what is haemorrhage
- failure of pro-hemostatic / pro-coagulation factors | - failure of hemostatic mechanism
63
ABNORMAL HEMOSTASIS what are 2 ways hemostatic mechanism can fail
1. problem with platelets | 2. problem with clotting factors
64
ABNORMAL HEMOSTASIS what are problems with platelets
1. not enough platelets (thrombocytopenia) | 2. abnormal platelet function
65
ABNORMAL HEMOSTASIS what are problems with clotting factors
1. heredity deficiency | 2. acquired deficiency
66
ABNORMAL HEMOSTASIS what causes acquired deficiency of clotting factors
1. antagonists | 2. vitk deficiency
67
ABNORMAL HEMOSTASIS what is thrombosis
excessive clotting
68
ABNORMAL HEMOSTASIS what are 2 causes of thrombosis
1. hereditary disorders | 2. acquired disorders
69
ABNORMAL HEMOSTASIS what are hereditary disorders
1. deficiency in naturally occurring anti coagulants | 2. deficiency in fibrinolytic factors
70
BLOOD GROUPS AND BLOOD TRANSFUSIONS what do antigens present on RBC mem act as
determinants of blood type
71
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antigen does almost everyone in the world have on their RBC s
H antigen
72
BLOOD GROUPS AND BLOOD TRANSFUSIONS where does H antigen come from
H gene converts precursor to H antigen
73
BLOOD GROUPS AND BLOOD TRANSFUSIONS what can H antigens be converted into
antigens of ABO blood type system
74
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antigen that H antigen gets converted into depend on
genes inherited from parents
75
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if A gene is inherited from parents
A gene gives rise to A enzyme
76
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens in presence of A enzyme
addition of another sugar molecule to end of H antigen to form antigen A
77
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if B gene is inherited from parents
B gene gives rise to B enzyme
78
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens in presence of B enzyme
addition of another sugar molecule to H antigen to form antigen B
79
BLOOD GROUPS AND BLOOD TRANSFUSIONS what does person w type A have
1. A gene | 2. A antigen
80
BLOOD GROUPS AND BLOOD TRANSFUSIONS what does person w type B have
1. B gene | 2. B antigen
81
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if A and B gene inherited
- A gene gives rise to A enzyme ==>. A antigen | - B gene gives rise to B enzyme ==> B antigen
82
BLOOD GROUPS AND BLOOD TRANSFUSIONS what does person with blood type AB have
1. A gene + antigen | 2. B gene + antigen
83
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if O gene is inherited
1. no A enzyme to give rise to A antigen | 2. no B enzyme to give rise to B antigen
84
BLOOD GROUPS AND BLOOD TRANSFUSIONS what does person with blood type O have
H antigen only
85
BLOOD GROUPS AND BLOOD TRANSFUSIONS what genes are dominant to O
1. A gene dominant to O gene | 2. B gene dominant to O gene
86
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can a person be blood type O
- inherit O gene from one parent | - inherit O gene from other parent
87
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can person be blood type A phenotype
- inherit A gene from one parent + A gene from other parent | - inherit A gene from one parent + O gene from other parent
88
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can person be blood type B phenotype
- inherit B gene from one parent and + B gene from other parent - inherit B gene from one parent + O gene from other parent
89
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can person be blood type AB phenotype
- inherit A gene from one parent + B gene from other parent
90
BLOOD GROUPS AND BLOOD TRANSFUSIONS where are antibodies present
plasma
91
BLOOD GROUPS AND BLOOD TRANSFUSIONS what is immune antibody
antibody for responding to non self
92
BLOOD GROUPS AND BLOOD TRANSFUSIONS what is naturally occurring antibody
antibody from responding to self
93
BLOOD GROUPS AND BLOOD TRANSFUSIONS what is example of naturally occurring antibodies
antibodies of ABO system
94
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antibody does person with antigen A not produce
antibody A
95
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antibody does person with antigen A produce
antibody B
96
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antibody foes person with antigen B produce
antibody A
97
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can a person be rhesus pos
- inherit D gene from one parent + D gene from other parent | - inherit D gene from one parent and d gene from other parent
98
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can person be rhesus neg
- inherit d gene from one parent + d gene from other parent
99
BLOOD GROUPS AND BLOOD TRANSFUSIONS what does rhesus pos blood type mean
possess D antigen
100
BLOOD GROUPS AND BLOOD TRANSFUSIONS what does rhesus neg blood type mean
do not possess D antigen
101
BLOOD GROUPS AND BLOOD TRANSFUSIONS what do people that are rhesus pos and rhesus neg lack
D antibody
102
BLOOD GROUPS AND BLOOD TRANSFUSIONS when can antibody D be produced in person
1. person Rh neg | 2. person exposed to antigen D
103
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if transfusion is mismatched
1. agglutination | 2. break down of RBC s
104
BLOOD GROUPS AND BLOOD TRANSFUSIONS what is agglutination
clumping of RBC (not blood clot)
105
BLOOD GROUPS AND BLOOD TRANSFUSIONS how can person's blood type be determined in vitro
1. obtain sample of blood from person 2. take out RBC s from sample 3. add anti A to RBC s 4. add anti B to RBC s
106
BLOOD GROUPS AND BLOOD TRANSFUSIONS what are you looking for when mixing RBC s of donor with antibodies in plasma of recipient
whether or not there is agglutination
107
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if there is no agglutination
donor can give blood to recipient
108
BLOOD GROUPS AND BLOOD TRANSFUSIONS what happens if there is agglutination
donor cannot give blood to recipient
109
BLOOD GROUPS AND BLOOD TRANSFUSIONS what is universal donor
O
110
BLOOD GROUPS AND BLOOD TRANSFUSIONS why is O universal donor
- no A antigen means no reacting with antibody A in plasma of person that is type B - no B antigen means no reacting with antibody B in plasma of person that is type A
111
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antibodies does person with type AB blood contain
none - possess antigen A - possess antigen B
112
BLOOD GROUPS AND BLOOD TRANSFUSIONS what is universal recipient
AB
113
BLOOD GROUPS AND BLOOD TRANSFUSIONS why is AB universal recipient
- no antibody A means no reacting with antigen A on RBC of person that is type A - no antibody B means no reacting with antigen B on person that is type B
114
BLOOD GROUPS AND BLOOD TRANSFUSIONS what antigens does person with type O have
none