Week 3 Flashcards

(59 cards)

1
Q

what is blood

A

suspension of cells in a solute of water, proteins and electrolytes

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2
Q

what is plasma

A

anticoagulated blood, in which the cellular components have been removed

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3
Q

what is serum

A

the liquid in blood that has been collected without an anticoagulant

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4
Q

what is plasma

A
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5
Q

what is the function of RBCs

A

deliver oxygen/CO2 to tissues

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6
Q

what are platelets

A

thrombocytes which are cell fragments, produced when large megakaryocytes break into pieces

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7
Q

what is the function of platelets

A

large role in blood clotting

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8
Q

what is the function of WBC’s

A

primarily involved in immune responses

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9
Q

what is endomitotic synchronous replication

A

when megakaryocytes grow until fragments come off

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10
Q

what happens after damage to a blood vessel

A

immediate vasoconstriction

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11
Q

what is extanguination

A

action of draining a person completely of blood

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12
Q

what happens after breakage of the endothelial cell barrier

A

recruitment of platelets from circulation forming a plug

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13
Q

what is platelet adhesion

A

when platelets interact with other cells, caused by collagen exposure

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14
Q

what is platelet aggregation

A

when platelets interact with each other, forming clots

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15
Q

what does platelet activation follow

A

stimulation by agonists such as ADP and thromboxane A2, or by direct interaction with the subendothelial matrix

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16
Q

what change occurs in the platelets

A

platelets convert from a compact disc to an irregular sphere shape, and granules in the cytoplasm secrete their contents

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17
Q

how is the loose plug formed

A

circulating platelets adhere to the initial layer of platelets

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18
Q

what is coagulation

A

the mechanism which leads to the conversion of soluble fibrinogen to insoluble rigid polymer fibrin

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19
Q

what is the clotting cascade

A

the mechanism by which fibrinogen is converted into fibrin

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20
Q

what are most activated coagulation factors

A

proteolytic enzymes which in the presence of cofactors cleave other factors in an ordered sequence

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21
Q

how is the intrinsic pathway activated

A

by exposed collagen and other negatively charged components of the subendothelium

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22
Q

what does activation of factor XII lead to

A

sequential activation of factors XI, IX, VIII, X and prothrombin

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23
Q

what leads to the activation of the extrinsic pathway

A

tissue factor complexes with factor VII leading to sequential activation of factors VII, X and prothrombin

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24
Q

what do both pathways result in

A

the final common girl, where activated factor X, in association with the cofactor Va in the presence of phospholipid and calcium, converts prothrombin into thrombin

25
how is fibrinogen converted into fibrin
thrombin splits the fibrinogen molecule and creates a polymer
26
what is prothrombin time
a measure of the function of the extrinsic pathway
27
what is the activated partial prothrombin time
a measure of the function of the intrinsic pathway
28
how is blood coagulation modulated
anti-thrombin, proteins C and S and TFPI
29
how does anti-thrombin modulate blood coagulation
inhibits the terminal proteins of the cascade, particularly factor Xa and thrombin. its activity is increased b interaction of heparin in the microvasculature and on the surface of the endothelial cells
30
how do proteins C and S modulate blood coagulation
- protein C is a vitamin K dependent plasma protein - which inactivates cofactors Va and VIIIa and stimulates fibrinolysis - protein C is converted to its active form by interaction with thrombin - protein S acts as a cofactor for protein C
31
how does TFBI modulate blood coagulation
tissue factor pathway inhibitor inactivates factor Xa and then TFBI/Xa complex inhibits factor VIIa within the VIIa tissue factor complex
32
when does fibrinolysis occur
when damaged epithelium is repaired
33
why must the fibrin thrombus be removed
to restore blood flow
34
what facilitates thrombus removal
a fibrin splitting protease, plasmin
35
what leads to the conversion of plasminogen to plasmin
release of tissue plasminogen activator (t-PA)
36
what does release of t-PA lead to
conversion of plasminogen to plasmin and then clot breakdown
37
what is circulating plasmin inactivated by
alpha2-antiplasmin
38
what happens to RBC's before they leave the bone marrow
they shed their nuclei
39
what is erythropoiesis
the production of RBC's
40
what regulates erythropoiesis
erythropoietin
41
what does the normal adult haemoglobin consist of
four polypeptide chains, 2 alpha and 2 beta
42
what is the affinity for oxygen in haemoglobin like
in the lungs it is high, in the tissue it is low
43
what is haematpoiesis
the development of haematopoietic elements
44
what four lineages extend from the myeloid lineage
1. erythroid 2. megakaryocytes 3. granulocytic 4. monocytic
45
what four cells extend from the lymphoid lineage
1. B-lymphocytes 2. T-lymphocytes 3. Natrual Killer cells 4. dendritic cells
46
where is erythropoitetin synthesised
mainly by endothelial cells in the kidney
47
what is the production of RBC's triggered by
tissue hypoxia
48
what are the 3 primary aims of treating a wound with severe bleeding
- to control bleeding - minimise effects of shock - minimise risk of infection
49
how should a wound with severe bleeding be treated
using a sterile dressing or a non-fluffy clan pad, with applied pressure
50
where are most growth factors produced
bone marrow
51
what is GMCSF
a growth factor for general stimulation of haemopoietic stem cells
52
what is symmetric division
cell replication in which both daughter cells can either be identical to the parent or different, but with a more restricted potential
53
what is asymmetric division
cell replication in which one daughter cell enters a differentiation pathway and gives rise to mature cells, while the other remains undifferentiated
54
list the types of potency from most to least
totipotent, pluripotent, multipotent, unipotent
55
what are the four types of shock
- obstructive - distributive - cardiogenic - hypovolemic
56
what is the primary structure
the amino acid sequence
57
what is the secondary structure
folded amino acid sequences forming alpha helices and beta pleated sheets
58
what is the tertiary structure
the three dimensional folding of the polypeptide
59
what is the quaternary structure
assembly of polypeptide subunits to form the overall functional protein