Final exam FC Flashcards

1
Q

There were two Polio vaccines, what is the main difference? How many people were accidentally injected with Polio?

A
  1. Attenuated live virus (weakened engineered virus)
  2. Dead virus (wasn’t dead and about 10,000 people got injected with this vaccine and contracted Polio)
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2
Q

What enzyme is responsible for cleaning up cellular debris in the lungs?

A

Trypsin

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3
Q

Trypsin is always_____.

What molecule keeps this enzyme in check?

A

active, but it’s activity is low and kept in check by alpha-1 antitrypsin.

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4
Q

1 in every 3,000 people have an inherited deficiency of alpha-1 antitrypsin. What are these people a good candidate for?

A

They are great candidates for lung transplants. This can buy them about another 30 years of life.

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5
Q

What are three things we talked about in class that can lead to chronic emphysema?

A
  1. alpha-1 antitrypsin deficiency
  2. smoke
  3. liver disease
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6
Q

Where is alpha-1 antitrypsin synthesized?

A

in the liver

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7
Q

What happens to Ferrous iron (Fe2+) in conditions of high oxidative stress?

A

It gets oxidized to Ferric iron (Fe3+) –> loses an e-

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8
Q

How much of our Hb is made up of Ferric iron? What significance does this have?

A

1.5% of our Hb is Ferric. This is why our SaO2 is 97.4% (Hb saturation from arteriolar sample)

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9
Q

What enzyme is responsible for reducing Fe3+ to Fe2+?

A

methemoglobin reductase (adds an e-)

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10
Q

If you have the sickle cell trait what can you do to reduce severity of symptoms?

A

Limit physical activity.

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11
Q

What causes sickle cell anemia?

A

The sickled RBC’s get stuck in the capillaries, eventually these RBC’s get pulled out of circulation and the body has to make new ones leading to anemia

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12
Q

What are two treatment options for sickle cell anemia?

A
  1. Transfusion of donor blood
  2. Hydroxyurea drug
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13
Q

How does Hydroxyurea work?

A

It turns on the fetal genes –> produces fetal Hb instead of the defective sickled Hb

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14
Q

What does sickle cell disease effect w/ regards to O2 and CO2 and Hb binding?

A

O2 is not released to the tissues where it is needed. Similarly, CO2 buildup can occur as is not able to bind to and get carried away by the Hb.

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15
Q

Sickle cell trait is beneficial how? (Why it is still lingering in the gene pool)

A

It is resistant to malaria

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16
Q

What is HbA1C?

A

acetylated Hb. Excess sugar can stick to Hb (A for adult and 1C is the position where the extra sugar hangs out)

17
Q

How much of our Hb is occupied by carbon monoxide? HbCO?

A

about 1 %

unless you smoke or work at an auto shop, then it can be higher

18
Q

Bicarb is a______ conjugate base than ____ is an acid…

A

stronger

CO2

19
Q

Why do patients with emphysema lose their drive to breathe if they have a high Hb saturation?

A

Their chemical receptors are looking at changes in pO2 to make pH adjustments since the body is chronically acidotic (high pCO2 and low pH)

20
Q

Why do we not use ALL the alveoli ALL of the time?
Why do we sigh/ yawn?

A

minimizes exposure to environmental irritants and alveolar damage
to open up or recruit alveoli that are not consistently used and disperses surfactant

21
Q

How often does the average adult sigh?

A

12-15x per hour

22
Q

If you have a really bad brain injury what areas can get physically separated and lead to apneustic breathing?

A

physical separation between the pons and the medulla