Protein & Amino Acid Metabolism Flashcards

(19 cards)

1
Q

What stimulates the uptake of amino acids into skeletal muscle, adipose tissue and the liver?

A

Insulin and growth hormone

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2
Q

What is the difference between ketogenic and glucose in amino acids?

A

The carbon skeleton is converted into alpha ketoglutarate

Vs succinate, fumerate, oxaloacetate, acteyl co A, pyruvate

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3
Q

What are the different avenues for protein excretion?

A

Urea 85%
Creatine 5%
Sweat as uric acid
Ammonia

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4
Q

When phenylalanine concentration falls what amino acid becomes essential?

A

Tyrosine

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5
Q

When methionine concentration falls, what amino acid becomes essential?

A

Cysteine

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6
Q

What occurs in transamination ?

A

A.a 1 + k.a 2 = A.a 2 + K. A 1

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7
Q

What are the two transaminases enzyme concentrations used to identify liver damage?

A

Alanine transaminase and aspartate transaminase

ALT and AST

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8
Q

What are the products of ALT?

A

Pyruvate and glutamate

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9
Q

What are the products of AST (aspartate transaminase)

A

Glutamate and oxoaloacetate

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10
Q

What are d amino acid oxidises?

A

They oxidase d amino acids so they aren’t used for protein synthesis because the proteins would be faulty.

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11
Q

what is Creatininine?

What can a high level indicate?

A

The breakdown product of creatine and creatin phosphate, present in urine in direct concentration to muscle mass.
Skeletal Muscle damage

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12
Q

What does a positive nitrogen balance indicate?

A

Growth, pregnancy, recovering from malnutrition

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13
Q

What is a negative nitrogen balance?

A

When the protein output is greater than input indicating trauma or infection.

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14
Q

What is PKU?

What test is there for it?

A

A hereditary disease causing faulty phenylalanine hydroxylase causing increased phenyl pyruvate concentrations
that results in impaired brain development as phenyl pyruvate prevents the uptake of pyruvate from mitochondria.
Newborn heel prick test

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15
Q

What compound is the toxic one in PKU?

What is the enzyme?

A

Phenyl pyruvate

Phenyl hydroxylase

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16
Q

What is homocystinuria?

A

Defect in methionine metabolism due to enzyme deficiency causing high {homocysteine} in blood.
Results in disorders in CT and muscle

17
Q

How does high [ammonia] affect the CNS

A

The metabolism uses alpha ketoglutarate, reducing turns of TCA and thus energy produced for brain cells

18
Q

How is ammonia processed?

A

Converted to urea in livers

Or used to synthesis glutamine where it is taken to the kidney and excreted as ammonia

19
Q

What enzyme in the neutrophil is responsible for synthesising ROS (superoxide) for respiratory bursts?

A

Membrane bound NADPH-oxidase