Hemoglobin Structure and Function Flashcards

1
Q

Ferrous iron is _____.

A

Fe2+

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2
Q

Ferric iron (Fe3+) cannot bind _____.

A

oxygen

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3
Q

Ferric iron in methemoglobin is reduced by ______.

A

cytochrome b5 reductase

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4
Q

What is P50?

A

P50 is the partial pressure value at which hemoglobin is half saturated.

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5
Q

Acidic solutions ____ the oxygen affinity of hemoglobin.

A

decrease

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6
Q

Increases in CO2 _____ the oxygen affinity of hemoglobin.

A

decrease

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7
Q

Temperature is _________ to the oxygen affinity of hemoglobin.

A

inversely proportional

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8
Q

2,3-BPG ______ the oxygen affinity of hemoglobin.

A

decreases

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9
Q

Alpha chains replace ______ chains.

A

zeta

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10
Q

Gamma chains replace ______ chains.

A

epsilon

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11
Q

Hemoglobin A2 functions like hemoglobin A. It is composed of ______.

A

alpha2/delta2

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12
Q

Heinz body anemia results from _____.

A

unstable hemoglobins precipitating in RBCs

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13
Q

Those with unstable hemoglobin disorders need ______.

A

folic acid (blood transfusions are usually unnecessary)

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14
Q

Disorders in which hemoglobin’s oxygen affinity is enhanced result in ____ RBC counts.

A

increased (because the Hgb doesn’t release O2 and the kidneys think the body is hypoxic)

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15
Q

Methemoglobinemia can be caused by _______, among other things.

A

cytochrome-b5 reductase deficiency, contaminated well water (with nitrates), and drugs such as benzocaine, sulfa, dapsone, and phenacetin

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16
Q

Methemoglobinemia can be treated with ______ (if metHgb levels are greater than 40%).

A

methylene blue

17
Q

In addition to competitively binding at the O2 sites, CO also ____ shifts the oxygen binding curve, thus making it harder for hemoglobin to release O2.

A

left

18
Q

High-affinity hemoglobins (such as Chesapeake hemoglobin) lead to ______.

A

erythrocytosis

19
Q

Chronic methemoglobinemia requires ______ for treatment, but acute methemoglobinemia levels greater than _____ require ______.

A

nothing; 30%; methylene blue

20
Q

Carboxyhemoglobin will give a falsely _____ pulse-ox reading.

A

high

21
Q

Hemoglobin Koln is a mutation in the ____ chain that results in ______ affinity hemoglobin.

A

beta; increased

22
Q

Hemoglobin Poole is a mutation in the _____ chain that results in _________ that resolves after birth.

A

gamma; infantile hemolytic anemia

23
Q

List three causes of cyanosis.

A

Excess deoxyhemoglobinemia (many causes)
Excess methemoglobinemia
Sulfhemoglobinemia

24
Q

Methemoglobin is _____ shifted.

A

left

25
Q

Hemoglobin M is __________.

A

methemoglobin

26
Q

CO poisoning _____ shifts the hemoglobin binding curve.

A

left