PSC1002/L02 Blood Flashcards

1
Q

What percentage of total body weight is blood?

A

8%

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2
Q

Give 3 functions of blood.

A

Gas transport and exchange
Distributing solutes
Immune functions
Maintaining body temperature
Regulates blood clotting
Preserving acid-base homeostasis
Stabilising blood pressure

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3
Q

What is blood composed of? (3)

A

Erythrocytes
Leukocytes
Thrombocytes

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4
Q

How does blood separate when centrifuged? (3)

A

55% soluble materials (top)
1% buffy coat - white blood cells and platelets
44% haematocrit (bottom)

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5
Q

What are the 2 main functions of plasma?

A

Thermoregulation
Transport

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6
Q

How does a high percentage of water in plasma affect properties? (3)

A

High specific heat capacity
Heat not needed lost to environment
Precentage of water determines blood viscosity/ bp

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7
Q

Describe serum albumins (3)

A

55% of plasma volume
Large protein synthesised in liver
Maintains osmotic pressure of plasma
Transport of lipids & steroid hormones

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8
Q

Describe globulins (3).

A

38% of plasma volume
Transport ions, hormones, lipids
Immune proteins made by leukocytes

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9
Q

Describe clotting proteins. (3)

A

7% plasma volume
Essential for blood clotting
Synthesised in liver

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10
Q

What makes up the final 1% of blood plasma?

A

Regulatory proteins
Enzymes, proenzymes, hormones

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11
Q

What does a normal electrophoretic pattern of plasma proteins show? (5)

A

Albumin, a1, a2, B and Y globulins

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12
Q

Give 3 causes of cirrhosis.

A

Cancer
Alcoholism
Viral hepatitis

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13
Q

What can cirrhosis lead to? (2)

A

Decrease in production of plasma proteins
Decreased colloidal osmotic pressure
Fluid loss to ECS
Severe edema in abdomen
Decline in clotting factor/easy bruising

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14
Q

What is the volume of erythrocytes?

A

80-96 femtolitres

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15
Q

Where are small/large RBCs found?

A

Small - macrocytic in iron deficiency anaemia
Large - microcytic in folate (vitamin B9)

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16
Q

Where does erythropoiesis occur?

A

Bone marrow

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17
Q

Describe the 7 steps in erythropoiesis.

A

Hematopoietic cell
Erythrocyte-CFU
Proerythroblast
Early erythroblast
Late erythroblast
Reticulocyte
Erythrocyte

18
Q

In which step of erythropoiesis does the hormone erythropoietin stop being produced?

A

3 - proerythroblast

19
Q

In which step of erythropoiesis is haemoglobin synthesised?

A

4 - early erythroblast

20
Q

In which step of erythropoiesis is the nucleus ejected?

A

5 - late erythroblast

21
Q

In which step of erythropoiesis are organelles ejected?

A

6 - reticulocyte

22
Q

How long after a bleed is homeostasis achieved in the blood?

A

26 days

23
Q

How are erythrocytes disposed of at the end of their life?

A

Phagocytosed in liver and spleen

24
Q

What are heme components recycled into? (2)

A

Heme into biliverdin then bilirubin, secreted in bile from liver
Iron stored by protein ferritin in liver

25
Q

Describe Glucose-6-phosphate dehydrogenase (G6PD).

A

Predisposes to red blood cell breakdown (haemolytic crisis) when exposed to certain environmental triggers

26
Q

Describe the 2 parts of a haemoglobin molecule.

A

Globin - 4 protein chains
4 iron containing haem groups

27
Q

Describe the structure of the Haem group.

A

Porphyrin ring containing 1 iron atom

28
Q

Describe the structure of iron with and without oxygen.

A

Without: Fe2+ (ferrous)
With: Fe3+ (ferric)

29
Q

Give the 4 forms of globin protein.

A

Alpha, beta, gamma, delta

30
Q

What are the 3 combinations of globin chains in adults?

A

HbA - 2A, 2B
HbA2 - 2A, 2D
HbF - 2A, 2Y

31
Q

What are the 2 forms of haemoglobin and where are they found?

A

r form - high O2 affinity e.g., in lungs
t form - low O2 affinity e.g., in peripheral tissues

32
Q

Give 3 other molecules that haemoglobin can bind.

A

Carbon dioxide
Acidic hydrogen portion of carbonic acid
Carbon monoxide
Nitric oxide

33
Q

What are haemoglobinopathies?

A

Abnormal haemoglobin chains

34
Q

What are thalassaemias?

A

Decreased amount of globin chains or absent globin chains due to gene expression defects

35
Q

Describe sickle cell anaemia. (3)

A

Mutation is B-globin gene
Glutamic acid replaced by valine
Creates sticky patches and HbS polymerisation

36
Q

How can thalassaemias occur? (2)

A

Gross deletion of one or more globin genes
Gene mutation

37
Q

Describe the 2 classes of thalassaemia.

A

a - production of a globin is deficient
b - production of b globin is deficient

38
Q

What form of haemoglobin is produced in a thalassaemia?

A

Excess B chains
Unstable tetramers of 4 B chains
HbH

39
Q

What happens to the oxygen dissociation curve in a thalassaemia?

A

High O2 affinity, reduced oxygen carrying capacity

40
Q

Why is B thalassaemia more clinically important than a thalassaemia?

A

Results in iron overload -> organ damage

41
Q

What does an excess of a chains lead to in B thalassaemia? (3)

A

Do not form tetramers
Bind to and damage RBC membranes
At high conc. form toxic aggregates
RBC are fragile and short-lived