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Cardiorespiratory > Constituents Of Blood > Flashcards

Constituents Of Blood Flashcards

1
Q

What are the 2 phases of blood?

A

Cellular component (45%):
Red cells form 99% of blood cells
White cells and platelets

Fluid component (55%):
Plasma

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2
Q

What is the volume of red blood cells called?

A

Haematocrit
Normal haematocrit is 0.45

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3
Q

What is haemopoiesis?

A

The process of the production of blood cells and platelets which continues throughout life

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4
Q

Where does haemopoiesis occur in adults?

A

Confined to the blood marrow

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5
Q

What are the most primitive cells?

A

Stem cells

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6
Q

What is the lifetime of different blood cells?

A

Red blood cells: 120 days
Platelets: 7-10 days
White blood cells: 6 hours

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7
Q

Where are the precursor cells in adults found?

A

Axial skeleton- skull, ribs, spine, pelvis and long bones

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8
Q

Where are the precursor cells in children found?

A

In all bones

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9
Q

What are hormonal growth factors?

A

Stimulate precursor stem cells to proliferate and differentiate

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10
Q

What are the types of hormonal growth factors?

A

Epo/Erythropoietin: (hormone made in kidney) red blood cells
G-CSF: (granulocyte colony stimulating factor) white cells
Tpo: platelets

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11
Q

What is haemoglobin?

A

Carries oxygen from the lungs to the tissues, where it transfers oxygen to myoglobin in muscles

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12
Q

What is haemoglobin formed of?

A

2 alpha and 2 beta chains
4 haem groups
Overall quaternary structure, due to the combination of more than two tertiary structures

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13
Q

What is anaemia?

A

Reduction in haemoglobin in blood

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14
Q

What is normal haemoglobin level?

A

12.5-15.5 g/dl
If lower: anaemic
If higher: polycthaemic ( caused by smoking, lung disease, inefficient lungs meaning less O2 is exchanged so more haemoglobin is required )

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15
Q

What are platelets?

A

Small cytoplasmic anucleate cells that block up holes in blood vessels

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16
Q

Where are platelets made?

A

Bone marrow from cells called megakaryocytes

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17
Q

What do platelets determine?

A

Determine bleeding time: PT (prothrombin time)

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18
Q

What is the lifespan of platelets?

A

5-10 days

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19
Q

What is reduced number in platelets called?

A

Thrombocytopenia (main risk is cerebral bleeding)
> 80 = increased bleeding
> 20 = spontaneous bleeding

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20
Q

What is high numbers in platelets called?

A

Thrombocytosis can lead to arterial and venous thrombosis leading to an increased risk of heart attack and stroke

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21
Q

What are coagulation proteins?

A

Enzymes produced in liver
They circulate in inactive form to make blood clot, converts soluble fibrinogen into soluble fibrin polymer

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22
Q

What is thrombin?

A

Makes platelet plug

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23
Q

Why is Vitamin K essential for coagulation proteins?

A

Essential for correct synthesis of coagulation factors (2,7,9 and 10)

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24
Q

What are plasma proteins?

A

Soluble and in plasma component

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25
Q

What is albumin?

A

Most numerous protein in plasma, produced in liver, maintain oncotic pressure
Lack of albumin results in oedema
Carries fatty acids, steroids & thyroid hormones

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26
Q

What are immunoglobulins?

A

Antibodies produced by plasma cells
IgB (most important)
IgM (all start as this)
IgA/IgE (produced in response to non-self protein antigens

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27
Q

When will an oxygen dissociation curve shift to the right?

A

When pH is decreased
When temperature is increased

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28
Q

When will an oxygen dissociation curve shift to the left?

A

When pH is increased
When temperature is decreased

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29
Q

Can red blood cells repair themselves?

A

No as they have no nucleus or mitochondria

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30
Q

What is a young red blood cell called?

A

Reticulocyte

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31
Q

What is Type A blood type?

A

Individuals always have anti-B antibodies in their plasma.
A antigen is co-dominant

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32
Q

What is Type B blood type?

A

Individual always have anti-A antibodies in their plasma.
B antigen is co-dominant

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33
Q

What is Type AB blood type?

A

Have neither anti-A or anti-B antibodies in their plasma, has A+B antigens on surface of red blood cells

UNIVERSAL RECIPIENT

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34
Q

What is Type O blood type?

A

Both anti-A and anti-B antibodies (has no A or B antigens) in their plasma

Type O is a UNIVERSAL DONOR since don’t have A or B antigens on surface of red blood cells

O antigen is RECESSIVE

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35
Q

What are anti-A/anti-B etc antibodies known as?

A

Anti-erythrocyte antibodies / Natural antibodies

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36
Q

What would happen if a Type A person was transfused Type B blood?

A

1) The anti-B antibodies in the recipients blood would attack the transfused blood

2) The anti-A antibodies in the donor blood would attack the recipients blood however this is usually of little consequence since the transfused antibodies become so diluted in the recipients plasma that they are ineffective at inducing a response

It is the destruction of the transfused cells by recipients antibodies that produces problems

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37
Q

What is Rhesus?

A

C,D,E antigens
D antigen is most important

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38
Q

What does Rhesus positive mean?

A

D antigen is present

39
Q

What does Rhesus negative mean?

A

D antigen is not present

40
Q

What are symptoms of anaemia?

A

Tiredness
Lethargy
Malaise
Reduced exercise tolerance
Shortness of breath on exertion
Angina

41
Q

What are signs of anaemia?

A

Palor
Pale mucus membranes
Palmar creases (pink hands)
Glossitis (sore tongue)
Angular stomatitis (cracking at corners of mouth)
Kylonychia (caused by iron deficiency) - spoon shaped nails

42
Q

What are classifications of anaemia?

A

Iron deficiency
B12 folate deficiency
Anaemia of chronic disorder
Haemolysis
Bone marrow failure/infiltration

43
Q

What is iron deficiency anaemia?

A

Iron is needed for haemoglobin production, lack of iron results in the reduced production of small red cells

44
Q

What is red cell size measured as?

A

MCV (mean cell volume)

Normal = 82-96 fl
Iron deficiency anaemia/low haemoglobin = < 80 fl

45
Q

What are causes of anaemia?

A

Bleeding:

Occult gastrointestinal: can affect anyone, most common cause of iron deficiency anaemia

Menorrhagia (heavy periods): occurs in premenopausal women only or those who’ve had repeated child birth

Diet: Not getting enough iron in diet, in the Uk the cause is never diet

Worldwide the most common cause of iron deficiency anaemia is diet

46
Q

What is macrocytic anaemia?

A

Can occur without anaemia, there will be a raised MCV (> 100 fl) but normal haemoglobin levels this can be caused by liver diseases, alcohol and hypothyroidism

47
Q

What is the cause of macrocytic anaemia?

A

Occurs due to a vitamin B12 or folate deficiency

48
Q

Why is Vitamin B12 and folate important?

A

Needed for DNA synthesis
With a B12 and folate deficiency red blood cells cannot be made in the bone marrow and so less is released leading to anaemia

This deficiency will affect all dividing cells, but bone marrow is most active so is affected first

49
Q

What are causes of B12 deficiency?

A
  • In the terminal ileum B12 absorption occurs, however intrinsic factors produced by the gastric parietal cells in the stomach is required for absorption to occur since B12 binds to intrinsic factor and is then absorbed.

Thus if the stomach is damaged can result in less parietal cells thus less intrinsic factor thus less B12 absorbed

  • An auto immune disease called pernicious anaemia causes the antibodies to be made against gastric parietal cells meaning less intrinsic factors can be produced so there is a B12 malabsorption and thus anaemia.

However the liver has a vast store of B12 which can last 4 years, thus pernicious anaemia has a slow onset

50
Q

What are the causes of folate deficiency?

A

Folate is found in vegetables and fruit
Malabsorption, due to celiac disease
Dietary, don’t eat enough fruit and vegetables

Increased need, due to haemolysis or anything that results in increased cell division can cause a folate deficiency

51
Q

What is haemolysis?

A

Normal or increased cell production but decreased life span < 30 days, red blood cells are destroyed before their 120 days lifespan

Congenital (present from birth)

52
Q

What is spherocytosis?

A

Blood cells are spherical, they get stuck in vessels easily

Dominant condition but variable penetrance

53
Q

What is pyruvate kinase deficiency?

A

Enzyme required to convert phosphoenolpyruvate to pyruvate is deficient, resulting in less ATP production and also a build up of phosphoenolpyruvate or G6PD deficiency

54
Q

What is sickle cell anaemia?

A

Defect in beta globin chain in haemoglobin
Red blood cells are sickle shaped thus get trapped in vessels easily

55
Q

What is Thalassaemia?

A

Mutation in haemoglobin chains
Beta is more common in India + Pakistan
Alpha is more common in East e.g. Thailand

56
Q

What is autoimmune?

A

Immune system that attacks own red blood cells, can be triggered by a blood transfusion due to the presence of foreign antibodies

57
Q

What is mechanical?

A

Fragmentation of red blood cells be mechanical heart valve, or intravascular thrombosis in DIC
(disseminate intravascular coagulation)

58
Q

What is HDFN?

A

Haemolytic disease of the foetus and newborn
Mother has Rhesus negative blood (RhD negative) and baby has RhD positive.

When mothers blood is exposed to babies blood in pregnancy, mothers immune system recognises foreign Rhesus positive blood and begins making antibodies against babies blood.

First baby is unaffected since it takes time for antibodies to be produced, the mother is said to be sensitised to Rhesus positive blood.

59
Q

What happens if the mothers second baby is also RhD positive?

A

When the mothers blood is exposed to babies, antibodies are produced immediately and begin destroying babies red blood cells, resulting haemolysis of foetus/newborn = anaemia/jaundice.

Whilst mother is carrying the baby, her antibodies can cross to baby via placenta and begin attacking

60
Q

What are white blood cells?

A

Normal white blood cells are mature cells that circulate in the blood, they are produced from immature precursor cells in the bone marrow which are derived from stem cells

Rate of production is under hormonal control of G-CSF

61
Q

What are neutrophils?

A

Release chemotaxins (signal more white blood cells to come to site) and cytokines, important in inflammatory response

Phagocytose and kill bacteria

Lack of number or function results in recurrent bacterial infections

Most numerous white cell - 10 hours

62
Q

What are lymphocytes?

A

B cells & T cells

Vital to immunity

Some generate antibodies against specific foreign antigens e.g. bacteria & viruses

Others are immunological memory - generates immunity and allows vaccination

63
Q

What are T lymphocytes?

A

Made in bone marrow

Mature in Thymus

Some are helper cells (CD4, help B cells in antibody generation), responsible for cellular or cell mediated immunity), some are cytotoxic cells (CD8)

64
Q

What is acute leukaemia?

A

Proliferation of primitive precursor cells usually found in bone marrow, proliferation without differentiation, replaces normal bone marrow cells

65
Q

What is acute myeloblastic leukaemia (AML)?

A

Malignant proliferation of the precursor myeloblasts (unipotent stem cells) in the bone marrow, disease primarily affects adults - 50% survive 5 years

66
Q

What is acute lymphocytic leukaemia (ALL)?

A

Malignant proliferation of the lymphoblast precursor cells in the bone marrow, disease primarily affects children - 80% cured

67
Q

What is high grade lymphoma?

A

Lymphocytes in lymph nodes become malignant, very similar to leukaemia

Classified as Hodgkins disease and Non-Hodgkins lymphoma (NHL), disease usually of the lymph nodes that spreads to the liver, spleen, bone marrow and blood

68
Q

What is homeostasis?

A

The arrest of bleeding, involving the physiological processes of blood coagulation and the contraction of damaged blood vessels

Blood is usually fluid inside blood vessels:
- Proteins of the coagulation cascade and the platelets circulate in an inactive state
- Proteins and platelets are only activated by tissue factor, which is present on every single cell apart from endothelial cells, so when endothelium is punctured blood comes into contact with tissue factor and thus starts clotting

69
Q

What happens it blood clots inside vessel?

A

Thrombosis

70
Q

What happens if blood fails to clot outside vessels?

A

Bleeding disorder

71
Q

What does bleeding result in?

A

Results in the beginning of the coagulation cascade:
- series of proteolytic enzymes that circulate in an inactive state being activated (usually by exposure to tissue factor) in a cascade or waterfall sequence

  • In order to generate the key enzyme Thrombin which cleaves fibrinogen creating fibrin polymerisation e.g. a blood clot
72
Q

What is coagulation cascade?

A

Very complex, multiple steps allow for biological amplification & allows for regulation

Can be graduated in response to severity of challenge

73
Q

What is haemophilia?

A

Recessive X-linked

Severe bleeding disorder; bleeding into muscles and joints, not enough clotting factors in blood = slow clotting time or long PTT (prothrombin time)

Only affects males since it’s X-linked inheritance

Females are carriers

74
Q

What is Haemophilia A?

A

Bleeding into muscles and joints
Rare: 1 in 10,000 males
Deficiency in clotting factor VIII (8)
Treat with factor VIII

75
Q

What is Haemophilia B?

A

Bleeding into muscles and joints
More rare: 1 in 50,000 males
Deficiency in clotting factor XI (9)
Treat with factor XI
Less common since gene is smaller

76
Q

What is Von Willebrands Factor (VWF)?

A

VWF is required for platelets to bind to damaged blood vessels, so lack of VWF = platelet dysfunction, hence muco-cutaneous bleeding

Usually a mild bleeding disorder

77
Q

What is muco-cutaneous bleeding?

A

Bleeding in skin and mucous membranes e.g. easy bruising, prolonged bleeding from cuts, nose bleeds (epistaxis), spontaneous gum bleeding/GI loss etc

Incidence up to 1% = common
Often unrecognised and undiagnosed

78
Q

What are acquired bleeding disorders?

A

Recent onset, not lifelong and no family history
May be generalised or localised bleeding

Most common cause: anti-platelet or anti-coagulation medication
Other causes: Liver disease

79
Q

What is Vitamin K deficiency caused by?

A

Caused by malabsorption - especially in obstructive jaundice

Treat with IV Vitamin K

80
Q

What does aspirin affect?

A

Platelet function

81
Q

What is heparin and warfarin and what do they do?

A

Most widely used oral anticoagulant
Works by inhibiting Vitamin K, affects coagulation cascade

82
Q

What do steroids do to tissue?

A

Makes tissues thin and causes bruising and bleeding

83
Q

What is disseminated intravascular coagulation (DIC)?

A

Breakdown oh haemostatic balance
Simultaneous bleeding and microvascular thrombosis
Life threatening condition

84
Q

What are causes of DIC?

A

Sepsis
Obstetric (anything that goes wrong with pregnancies)
Malignancy

85
Q

How is a platelet plug formed?

A

When a vessel is injured/ruptured, this disrupts the endothelium, resulting in the exposure of collagen

Platelets adhere to the collagen fibres via an
intermediary called (VWF)

The platelet adheres to the factor, which itself is adhered to the collagen via a receptor on the platelet membrane called the glycoprotein 1B receptor

86
Q

What does the binding of platelets to the collagen fibre wall cause?

A

Triggers the platelet to release the contents of their secretory vesicles via exocytosis

This includes platelet dense granules, which are also released upon cell activation, from these granules ADP is released which acts on the P2Y1 and P2Y12 causing platelet amplification

87
Q

What is platelet activation?

A

Thrombin binds to PAR1 and PAR4 receptors, inducing platelet activation and further thrombin release

This results in the platelet changing shape from a smooth discoid shape to a more spiculated (spiky) with pseudopodia, this increases the surface area of the platelet

88
Q

What does platelet activation cause?

A

Causes an increase in the expression of glycoprotein IIb/IIIa (GPIIIb/IIIa) receptors on the platelets which binds to fibrinogen (from alpha granules) enabling new platelets to adhere to old ones, a positive feedback mechanism called platelet aggregation

89
Q

What do platelet plugs do?

A

Completely seal small breaks in vessels
Its effectiveness is enhanced by its other property which is contraction

Platelets contain a very high concentration of actin and myosin, resulting in compression and strengthening of the platelet plug

90
Q

What is the primary mechanism used to seal breaks in vessel walls?

A

Platelet plug

91
Q

What is coagulation cascade?

A

Blood coagulation or clotting is the transformation of blood into a solid gel called a clot or thrombus which consists mainly of a protein polymer called fibrin

Clotting occurs locally around the platelet plug and is the dominant haemostatic defence - its function is to support and reinforce the platelet plug and to solidify blood that remains in the wound channel

The cascade can be divided into two parallel pathways, extrinsic and intrinsic

Under physiological conditions, the pathways are in fact not parallel but instead are activated sequentially with thrombin serving as the link between them

92
Q

What happens in the intrinsic pathway?

A
93
Q

What happens in the extrinsic pathway?

A

Cardiorespiratory (27 decks)

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