11-21 L4 Iron metabolism & Iron disorders Flashcards

1
Q

Define two sources of iron and there bioavialability

A
  • heme (15-30%)
  • nonheme (5-15%)
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2
Q

Fe is absorbered into the enterocyte by what trasporter?

what 2 things inhibits this transport (this inhibition molecule is found in what?)

A
  • DMT1 (H+ 2ndary active transporter
    • (sreving Fe2 but not Fe3)
  • Inhibited by
    • Cd (candium)
    • high concentration of Ca
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3
Q

Name 2 promoting factors of iron

A
  • Heme
  • Ascorbic acid
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4
Q

What mediates cellular iron export?

what hormone controls it?

A
  • ferroprotin mediates cellular iron export
  • hepcidin
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5
Q

What does hepcidin do?

(RAP)

A
  • R: decreases fe recycling (macrophages)
  • A: decreases intestinal Fe absorption
  • P: decreased ciruculating Fe2Tf pool
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6
Q

Name 2 iron-refractory iron deficiency anemia

A
  • Mutations in matriptase
  • Iron-refractory iron-deficiency anemia
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7
Q

Hereditary hemochromatosis type 1 (iron overload)

what is the mutation

A
  • mutation in HFE
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8
Q

Hereditary hemochromatosis type 4 (iron overload)

what is the mutation

A
  • Ferroprotin
  • Autosomal dominant
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9
Q

What is teh cause of iron toxicity?

what type of general damage does it do?

A
  • by-product of iron oxidation (Fe2–>Fe3)
  • causes lipid peroxidation, damage to DNA enzymes, polysaccharides
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10
Q

what is the mainstay treatment of Hereditary iron deficiency?

A
  • repeated phleobotomy
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11
Q

What is the leading cause of death in Beta-thalaseemia patients?

treatment?

A
  • iron overload
  • cardiomyopathy (iron overload)

iron chelators

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12
Q

how does IDA (iron deficiency anemia) appear?

A

microcytic hypochromic anemia

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13
Q

Iron deficiency beings with what?

how do we treat it?

A
  • beings with depletino of Fe stores
    • once you see hypochromic microcytic that means you have been iron def for awhile
  • Treatment
    • oral Fe supplementation (parenteral Fe)
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