Gas pressures and haemoglobin Flashcards

1
Q

what does 1kPa equal?

A

7.5mmhg or 1000N/m2

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2
Q

What does Dalton’s law state?

A

Dalton’s law states that the total pressure is equal to the sum of the component partial pressures.

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3
Q

what is atmospheric pressure?

A

~100kPa

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4
Q

what is PO2?

A

21kPa

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5
Q

the partial pressure of a gas in solution is equal to

A

that in gaseous form at equilibrium

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6
Q

what does Henry’s law describe?

A

the solubility of a gas.

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7
Q

[gas] =

A

partial pressure x solubility coefficient

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8
Q

state the normal Po2, hb saturation and O2 content of mixed and arterial blood.

A

arterial blood:
PO2= 13.3kPa
97-98% Hb saturation
200ml/l O2 content

Mixed blood:
PO2= 5.3kPa
75% Hb saturation
150ml/l of O2 content

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9
Q

how much of the O2 is used per cycle?

A

1/3

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10
Q

Oxygen is carried in what two forms?

A

dissolved in plasma and bound to haemoglobin

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11
Q

O2 carried in which form is directly related to PaO2?

A

dissolved in plasma

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12
Q

what are the normal range of Hb content of blood?

A

females: 11.5-16g/100ml
males: 13.5-18g/100ml

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13
Q

what is the resting O2 consumption?

A

250ml/ min

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14
Q

what is the role of haemoglobin?

A

haemoglobin allows efficient transport of high amount of O2 to meet demands at a normal cardiac output.

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15
Q

how does O2 move from alveolar air to lung capillaries?

A

O2 diffuses down the partial pressure gradient (13.3 –> 5.3kPa)

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16
Q

how is O2 delivered to tissues?

A

O2 diffuses from capillary to tissues which are using O2 and therefore have a lower PO2.

17
Q

Describe the structure of Hb

A

Haemoglobin is made of 4 subunits, each subunit consisting of a peptide globin chain and a haem group. each subunit will bind one molecule of O2

18
Q

1g of Hb will bind how much O2?

A

1.36ml

19
Q

what is average Hb concentration?

A

15g/100ml

20
Q

what is the normal O2 content?

A

200ml/ L

21
Q

describe the components of adult/ foetal and HbA2 haemoglobins?

A
HbA:
- 2 alpha chains and 2 beta chains
HbA2:
- 2 alpha chains and 2 delta chains
HbF:
- 2 alpha chains and 2 gamma chains
22
Q

when does the switch occur from embryonic haemoglobin to foetal haemoglobin?

A

13 weeks gestation

23
Q

what is the Hb concentrations of newborn?

A

80% HbF and 20%HbA

24
Q

when is the foetal Hb replaced by adult Hb?

A

at 3-6 months of age

25
Q

what are the commonest genetic disorders?

A

genetic defects in globin chains are the commonest of all genetic disorders

26
Q

what are the thalassaemias?

A

Thalassaemias are inherited disorders caused by defects in alpha or beta globin chain synthesis. this leads to imbalance of chains resulting in decreased synthesis of RBC and increased breakdown of mature RBCs. This impairs O2 carrying capacity. alpha thalassaemia is worse than beta thalassaemia as it is present in all forms of Hb.

27
Q

describe the cause and course of sickle cell disease.

A

sickle cell disease is caused by a point mutation in the beta chain. it is recessive- one copy of faulty gens –> HbAS = sickle cell trait, generally asymptomatic, anoxia manifesting in stress such as air travel, confers protection against malaria; 2 copies –> HbSS = sickle cell disease: symptoms variable from asymptomatic to death, increased turnover of cells can lead to severe haemolytic anaemia, severe pain due to vaso-occlusive crises and infarction.

HbS decreases the flexibility of the cell leading to a characteristic sickle shape. sickling leads to shortened erythrocyte survival and impaired flow through circulation.