Ammonia Metabolism Flashcards

1
Q

NH4+ cannot cross membranes easily while NH3 can. (T/F)

A

T

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2
Q

Where do AA first go when transported into the blood after digestion?

A

The Liver

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3
Q

What type of pump drives AA into the cell from the lumen of the intestine?

A

An Na+ pump. (Secondary active transport)

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4
Q

Name the the compound of these species after deamination. Also, what are their functions?

Glutamate

Aspartate

Alanine

Glutamine

A

a-ketoglutarate The amino group pool of the cell

oxaloacetate Donates nitrogen to the urea cycle

pyruvate A key role in gluconeogenesis

glutamate Transports nitrogen to liver for urea cycle

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5
Q

Glucagon, cortisol, epinephrine and norepinephrine all [ ] mobilization of stored fuels.

A

promote

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6
Q

What are two key AA that leave cell when fasting?

A

Glutamine and Alanine

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7
Q

alpha-ketoglutarate (a-KG) acts as the universally accepts what?

A

amine groups

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8
Q

What does alanine get broken down into while in the fasted state? Where does this take place?

A

Glucose (which goes back to muscle) and Urea.

The liver.

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9
Q

Glutamate dehydrogenase and glutamine synthase can add free ammonium to “fix” it as glutamine. These reactions require energy. (T/F)

A

T

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10
Q

Which AA activates the production of NAG which then activate CPSI in the Urea Cycle.

A

Arginine

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11
Q

Name two broad conditions where the urea cycle would function on a high level.

A

Starvation and a high protein diet.

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12
Q

High NH4+ levels in the blood point to a problem with:

A

The Urea Cycle

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13
Q

Elevated urinary oratic acid suggests what?

A

A mutation close to carbamoyl phosphate

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14
Q

In the Urea Cycle, if the the ornithine / citrulline antiporter is defective, what condition would you associate with this defect?

A

HHH, (hyperammonaemia, hyperornithaemia, homocitrullinaemia)

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15
Q

N-carbamoylglutamic acid lowers NH4+ levels so it deactivates CPSI (T/F)

A

F, it does lower NH4+ levels, but it activates CPSI. (It replaces NAG if NAG is deficient)

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16
Q

[ ] and [ ] are used to make amino acids excretable in the urine.

A

Phenylbutyrate and benzoic acid