Micronutrients (Essential Trace Minerals) Flashcards

1
Q

What are the two forms that iron is found in food

A
  1. Heme (poryphorin ring of hemoglobin and myoglobin) - in animals
  2. non-heme (plants)
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2
Q

Which two states of iron are stable in the aqueous environment of the body and in food?

A

Fe3+ and Fe2+

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3
Q

What are the functions of iron?

A
  • oxygen transport (hemoglobin/myoglobin)
  • redox rxns
  • iron metalloenzymes
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4
Q

Is the RDA for iron higher in men or women? why?

A

women due to menses (also higher in pregnant women to cover fetus needs)

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5
Q

What is the difference between how heme and non-heme iron are absorbed?

A
  • non-heme: Fe3+ must be converted to Fe2+ by reductase enzyme to be absorbed by DMT1 (divalent metal transporter 1)
  • heme: absorbed as-is by HCP1 (heme carrier protein 1) and then broken down by heme oxygenase in intestinal cells to release Fe2+ and protoporphyrin
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6
Q

What are the three fates of Fe2+ after being absorbed?

A
  1. used in intestinal cells
  2. stored as ferritin in intestinal cells
  3. transported into blood by ferroportin
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7
Q

What are chelators?

A
  • small organic compounds that form a complex with a metal ion
  • can enhance absorption (if soluble)
  • can inhibit absorption (if insoluble)
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8
Q

How is iron transported in the blood?

A

as Fe3+ bound to transferrin carrier protein
(unbound Fe2+ is highly reactive ; can easily lose an electron and form free radicals)

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9
Q

What is the difference between ferritin and hemosiderin in the storage of Fe3+?

A
  • Ferritin - iron is readily available
  • Hemosiderin - iron is poorly available
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10
Q

How is Cu2+ absorbed and transported?

A
  • Cu2+ must be released from bound amino acids by HCl and pepsin to be absorbed
  • Cu2+ must be reduced to Cu+ to be absorbed
  • specific transporters in small intestine
  • transported to liver bound to protein where it is incorporated into ceruloplasmin
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11
Q

What is Menke’s disease?

A

X-linked genetic disease (gene ATP7A) where the body cannot absorb enough copper

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12
Q

What is Wilson’s disease?

A

excess copper that cannot be excreted in bile due to a mutation in ATP7B gene which causes copper to accumulate in the brain, kidneys and eyes after the liver reaches capacity

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13
Q

What are the main functions of zinc?

A
  • metalloenzymes that stabilize tertiary structure of a protein and play roles in reaction site of an enzyme
  • oxidant defense
  • DNA binding (Zn fingers)
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14
Q

How is Zinc absorbed?

A
  • must be released from amino acids before absorption - HCl and digestive enzymes in small intestine
  • carrier mediated absorbance (ZIP4) or simple diffusion
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15
Q

Is the RDA for zinc higher in men or women? Why?

A

Men, to support testosterone function

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