RBC physiology & function Flashcards

1
Q

What are the ways the function of Hb can be altered (4)

A
  • amount of Hb produced
  • Structure “””
  • stability “””
  • function “””
  • 2+ can affect each other => compound effect
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2
Q

What’s how does thalassemia affect Hb function? And how it occurs

A
  • Decrease production => Low Hb made

- due to mutation in globin genes (alpha = a thalassemia or beta= B thalassemia)

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3
Q

What’s how does haemoglobinopathies affect Hb function?

A

alters Hb Structure & function

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4
Q

Outline how the presence of haemoglobin S may affect the haematological characteristics of an individual

A

HbS forms bc glutamic acid is replaced valine @ 6th position on B-chain => sickle cell shape (when deoxygenated)

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5
Q

Where & how haeme & globin is formed to form haemoglobin?

A
  • in the mitochondria of RBC.
  • Fe2+ binds to prtoporphyrin IX ring & the center
  • transported to the cytoplasm to combine w/ globin
  • globin tetramer made in cytoplasm w/in polyribosomes: alpha + non-apla (beta or gamma)
  • ratio of haeme & globin should be close to 1:1 ratio
  • goblin tetramer + haeme = haemoglobin
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6
Q

Where & how is globin formed?

A

in the cytoplasm of RBC

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7
Q

Which stage in life are primitive haemoglobin, HbF and HbA predominant.

A
  • Embryo: primitive Hb
  • Foetus: HbF
  • 6 months old: HbA (if things are normal)
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8
Q

Why is the Embden-Meyerhofglycolytic pathway necessary for RBC function?

A
  • must have glycolytic pathway => energy (2 ATP / glucose)
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9
Q

Why is the hexose monophosphate shunt necessary for RBC function?

A
  • use ~10% glucose to produce NADPH => reduced glutathion (GSSG) w.\/ glucose-6-phosphate dehydrogenase
    > protect RBC from oxidative damag
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10
Q

Why is the Leubering-Rapaport shunt necessary for RBC function?

A

form 2,3-biphosphosphoglycerate (2,3 BPG)

> modify Hb affinity for O2

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11
Q

Why is the methaemoglobin (metHb) reductase necessary for RBC function?

A

rapidly convert metHb (Fe3+) to Hb (Fe2+) so Hb remains functional

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12
Q

What happens when there is a deficiency in glucose-6-phosphate dehydrogenase?

A

RBC can’t make reduced glutathione susceptible to oxidative damage => Hb denatured => heinz bodies
- so body increases erythropoiesis to compensate for RBC lost

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13
Q

measurement of Hb

A
  1. mix sample w/ Drabkin’s reagent
  2. reagent binds to Hb => cyanohaemaglobin (HbiCN)
  3. measure absorbance @ 540nm => [Hb}
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