B5-061 AA Metabolism Flashcards

(52 cards)

1
Q

calculate nitrogen intake from protein in diet

A

daily protein (g)/6.25

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2
Q

conditions that necessitate a positive nitrogen balance

3

A
  • pregnancy
  • body builder
  • a growing child
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3
Q

consuming the correct amount of protein should result in a

A

zero nitrogen balance

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4
Q

released from muscle due to protein breakdown

A

alanine

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5
Q
  • transports nitrogen
  • transfers carbons to the liver for GNG
A

alanine

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6
Q

the brain can use […] as an alternative to glucose

A

ketone

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7
Q

what lab values would be elevated as a result of ketone body metabolism due to a low calorie diet?

2

A

acetoacetate
B hydroxybutyrate

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8
Q

elevated BUN indicates increased […] catabolism

A

amino acid

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9
Q

9-4-4 rule of thumb for calculating calories from diet

A

9 fatty acid
4 carbohydrate
4 protein

calories/gram

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10
Q

proteins have [..] calories/gram

A

4

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11
Q

in fed states, excess AA are converted to

2

A

glucose
FA

stored in liver

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12
Q

where does the urea cycle occur?

A

liver

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13
Q

where does AA catabolism occur?

A

peripheral tissues

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14
Q

what vitamin acts as a coenzyme in transaminase reactions?

A

B6 (pyridoxal phosphate)

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15
Q

chemical reaction that transfers and amino group to a ketoacid to form new amino acids

A

transamination

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16
Q

transamination reactions

3

A
  • alanine -> pyruvate
  • aspartate -> oxaloacetate
  • glutamate -> a-ketogluterate
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17
Q

deamidation + transamination reaction

A

Asn -> Asp -> oxaloacetate

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18
Q

dehydratase reactions

2

A

serine -> pyruvate
cysteine -> pyruvate

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19
Q

a-ketogluterate
oxaloacetate
pyruvate

glucogenic or ketogenic?

A

glucogenic

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20
Q

anthing with Acetyl-CoA cannot be used to make

A

glucose

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21
Q

carbons that can be used to generate ketone bodies and fat, but not glucose

22
Q

the two inputs into the urea cycle

A

glutamate
aspartate

23
Q

how do we get glutamate for the urea cycle in the starved state?

A

a-ketoglutarate + alanine –> glutamate

transaminase reaction

24
Q

a ketoglutarate can be generated from

A

alanine via pyruvate

25
how do we get aspartate for the urea cycle in a starved state?
26
what AA can the liver make, even in a starved state? | 3
alanine aspartate glutamate
27
AA that is main focus in the liver during starvation
alanine
28
AA that is main focus in the kidney during starvation
glutamine
29
byproduct of glutamine to glucose production found in urine
ammonia
30
tyrosine is not typically considered an essential amino acid, but is for patients with [...]
phenylketouria | cannot make Tyr from Phe
31
essential amino acids | PVT TIM HALL
Phenylalanine Valine Tryptophan Threonine Isoleucine Methionine Histadine Arginine Lysine Leucine | PVT TIM HALL
32
excess protein is
catabolized
33
fat cannot be converted to
sugar
34
excess fatty acids are stored as
fat
35
there is [...] of carbon from Acetyl CoA to PEP
no net flux
36
any disruption in the urea cycle will cause
hyperammonia | reduced urea formation
37
the urea cycle involves enzymes in the | where in the cell
cytosol and mitchondia
38
BUN and urinary urea nitrogen indicate protein catabolism [...] the urea cycle | before or after
after
39
during starvation, do we expect an increase in BUN or Urinary Urea Nitrogen?
both
40
nitrogen balance is a simple consideration of nitrogen [...] vs nitrogen [...]
in out
41
a negative nitrogen balance indicates a need to [...] protein in the diet
increase
42
if the nitrogen is removed from alanine the remaining carbon backbone is a
pyruvate
43
AA made in the urea cycle but still considered essential in the diet
arginine
44
someone with PKU lacks what enzyme?
phenylalanine hydroxylase | converts Phe to Tyr
45
a primary site for amino acid catabolism in the well fed state is in the
liver
46
a [....] amino acid can be catabolized into metabolites used to make lipids
ketogenic
47
in the starved state, there are high levels of catabolism in the [...] that lead to increased levels of [...] in the blood
muscle alanine
48
transaminase use the [...] form of vitamin B6 as a cofactor
pyridoxal phosphate
49
after a transmaminase removes a nitrogen from an amino acid....
it remains bound to the enzyme until transferred to a different carbon skeleton | modified enzyme state
50
urea is a product of cleaving the end of
arginine
51
the two nitrogens of urea are derived from
aspartate and ammonia
52
blood urea decreases in what disorders? | 3 examples
* liver failure * pregnancy * urea cycle disorders