Protein Breakdown And Urea Formation Flashcards

1
Q

How do proteins enter the body and what are they broken down into?

A

Food

Amino acids

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2
Q

What is the normal ratio of amino acids:body protein?

A

50:50

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3
Q

How is the carbon skeleton formed from amino acids?

A

The nitrogen is taken off

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4
Q

What is the carbon skeleton used for?

A

Glucose generation
ATP source
Generation of ketone bodies

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5
Q

What happens to the nitrogen that is removed from amino acids?

A

Broken down in the liver to form urea and is excreted by the kidney

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6
Q

What is positive nitrogen balance?

A

There is a build up of body proteins- the amino acid pool is directed towards the making of new proteins

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7
Q

When does positive nitrogen balance occur?

A

During pregnancy or growth
Exercise and tissue hypertrophy (build up of new muscle protein)
Response to anabolic hormones

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8
Q

What is negative nitrogen balance

A

A loss of body protein which leads to increased urea production

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9
Q

When does negative nitrogen balance occur?

A

Wasting diseases, burns, trauma

Response to either an increase in catabolic or a reduction in anabolic hormones (diabetes)

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10
Q

What are the two things that happen to amino acids?

A

Used or broken down- NEVER STORED

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11
Q

What enzymes facilitate the removal of nitrogen?

A

Transaminase or aminotransferase

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12
Q

What happens in transamination?

A

Amino acid A + alpha keto acid B-> alpha keto acid A and amino acid B

Basically the NH3 group is transferred from amino acid A to amino acid B

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13
Q

Give some examples of alpha keto acids

A

Alpha ketoglutarate
Pyruvate
Oxaloacetate

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14
Q

What are two of the most important transaminases?

A

Alanine (ALT) and aspartate (AST)

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15
Q

What does aspartate + alpha ketoglutarate produce?

A

Glutamate and oxaloacetate

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16
Q

In the liver what are oxaloacetate and alphaketoglutarate used to make?

17
Q

In muscle, where can pyruvate be used?

A

In the TCA cycle and ETC to make ATP

Also gluconeogenesis

18
Q

What is high levels of AST and ALT in the blood indicative of?

A

Tissue damage- esp in liver and cardiac muscles

19
Q

What is the enzyme involved in the formation of amonnia?

A

Glutamate dehydrogenase

20
Q

What is the formation of ammonia process known as?

A

Oxidative deamination

21
Q

Free ammonia + glutamate ->?

22
Q

What enzyme does the ammonia + glutamate reaction use?

A

Glutamine synthase

23
Q

How is AA nitrogen transferred to urea (3steps)?

A

Transamination, formation of ammonia. Synthesis of urea

24
Q

Where does the urea cycle take place?

A

Mitochondria and cytoplasm

25
What are the substrates for the urea cycle?
Bicarbonate, aspartate and ammonium ions
26
CO2+ NH4 ->?
Carbonyl phosphate
27
Carbonyl phosphate + ornithine ->?
Citrulline
28
Citrulline + aspartate ->?
Argenine succinate
29
What are used for exercise in muscles during prolonged exercise or starvation?
Branched aas: | Leucine, isoleucine and valine
30
How does ammonia get from the peripheral tissues to the liver?
Most synthesise glutamine from glutamate Glutamine then travels to the liver where glutamate is made Glutamate undergoes transamination to form pyruvate Pyruvate used to synthesis glucose
31
What is the glucose Alanine cycle?
Glucose metabolised to pyruvate in tissue | Pyruvate then used in transamination to form alanine which is transported back to the liver
32
What are ketogenic amino acids?
Isoleucine, leucine, Tryptophan, phenylalanine, tyrosine, lysine
33
What are ketogenic amino acids broken down to form?
Acetyl CoA
34
What are glutagenic amino acids?
Alanine, cysteine, glycine, serine, threonine, tryptophan, valine
35
What happens to glutagenic amino acids?
Broken down and fed into TCA cycle and at the point of phosphoenolpyruvate used to make glucose