Blood function Flashcards

(39 cards)

1
Q

What are the 3 key functions of the blood?

A

Transport
Regulation
Protection

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2
Q

What are the 4 features of transport?

A
  • Respiration
  • Nutrient carrier from GIT
  • Transportation of hormones form endocrine gland
  • Transport of metabolic waste
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3
Q

What are the 3 features of regulation?

A
  • Regulation of pH
  • Regulation and maintenance of body temperature
  • Maintenance of cells’ water content
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4
Q

What are the 3 features of Protection?

A
  • WBC protect against disease by phagocytosis
  • Reservoir for substances such as water, electrolytes, etc
  • Haemostasis
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5
Q

What is the composition of blood?

A

Plasma (55%)
Buffy coat- leukocytes and platelets (<1% of whole blood)
Erythrocytes (45% of whole blood)

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6
Q

What is whole blood?

A
  • Slightly alkaline (pH- 7.35-7.45)
  • 8% of body weight
  • 5x more viscous than water
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7
Q

What is plasma?

A
  • Straw coloured and sticky
  • 55% of bodies total blood volume
  • 90% water
  • Solutes include proteins and non-proteins
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8
Q

What is the composition of plasma?

A
  • Albumin (60%)
  • Globulins (35%)
  • Fibrinogen (4%)
  • Other (<1%)
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9
Q

What are the features of albumin?

A
  • Globular protein
  • Synthesised in liver
  • Plasma conc of 35-50mg/mL
  • 19 day half life
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10
Q

What is the function of albumin?

A
  • Maintains oncotic pressure
  • Controls pH
  • Binding and transport- hormones, nutrients, metal ions, drugs, etc
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11
Q

What is a1 globulin?

A

a1- antitrypsin
Important in inflammation

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12
Q

What is a2 globulin?

A

Example= hepatoglobin, facilitates Hb clearance
a2- macroglobin, antiprotease binds to cytokines & GF

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13
Q

What is b-globin?

A

Example: transferrin, iron binding & transport
Plasminogen pre-cursor of plasmin & WBC migration

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14
Q

What is y- globin?

A

IgG (75%), IgA (15%), IgM (10%), IgD (0.2%), IgE (0.002%) fight off infection

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15
Q

What is Fibrinogen?

A

2nd Haemostasis, wound healing, inflammation, forms fibrin fibres- used for blood clotting

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16
Q

What is the other <1%?

A
  • Coagulation factors & inhibitors
  • Electrolytes
  • Nutrients
  • Hormones
17
Q

What are Leukocytes?

A

White blood cells

18
Q

What are Erythrocytes?

19
Q

What are Thrombocytes?

20
Q

What do Haematopoietic stem cells form?

A

Common myeloid progenitor
OR
Common lymphoid progenitor

21
Q

What do common myeloid progenitors form?

A

Erythrocytes
Mks= platelets
Myeloblasts

22
Q

What do myeloblasts form?

A

Basophil
Neutrophil
Eosinophil
Monocyte

23
Q

What does common lymphoid progenitor form?

24
Q

What does a lymphoblast form?

A

T or B lymphocyte

25
What are agglutinogens?
Antigens Specific proteins located on RBC wall- basis for blood group classification
26
What are Agglutinins?
Antibodies Plasma antibodies that act against agglutinogens not present on a persons own RBC
27
What is the universal recipient?
AB+
28
What is the universal donor?
O-
29
what is Rhesus (Rh) blood group
- Based on ion- channel antigen on RBC membrane - Rh- more common in the west (15%) than in Asia or Africa (1%)
30
What is the humoral reaction to Transfusions?
Blood from type A donor Type B recipient Donor RBCs agglutinated by recipient plasma Agglutinated RBCs block small vessels
31
What is the cellular reaction to Transfusion?
Immune cells
32
What is the Haemolytic disease of the Newborn (HDN)
First pregnancy= Protected by the placenta blood barrier, mother not exposed to Rh agglutinogens until the time of childbirth Second pregnancy= Antibodies cross barrier, child born with severe anemia
33
What is the treatment for HDN?
Use anti- Rh gamma globulin to mask Rh agglutinogens
34
What is Primary Haemostasis?
-Damage to blood vessel wall - Vasoconstriction - Platelet adhesion & activation - Granule release- increase conc of platelet activators, coagulation factors, vasoconstrictors - Platelet plug formed
35
What is secondary Haemostasis?
damage to blood vessel wall formation of "sticky" platelet plug formation of insoluble fibrin clot
36
What is the activation of coagulation?
Intrinsic pathway FXII Extrinsic pathway FVII Common pathway FX Fibrinogen- Fibrin Crosslinking formed
37
Where does anticoagulation act?
Intrinsic pathway & Common pathway
38
Where does Fibrinolysis (plasmin) occur?
Fibrin
39
What is TXA?
Fibrinolysis inhibitor Stops breakdown of fibrin fibres Stops rapid bleeding