Protein synthesis and the urea cycle in liver disease Flashcards

1
Q

Amino acids split into

A

alpha-Keto acids and NH4+

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2
Q

Where does the alpha-keto alpha acids go and used in?

A

Go to citric acid cycle for respiration

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3
Q

Where is the enzyme alanine amino-transferase found?

A

Muscle and liver.

High levels of ALT may be a sign of liver damage from hepatitis, infection, cirrhosis, liver cancer, or other liver diseases

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4
Q

Why is the liver important in protein break down?

A

Stores more proteins than other tissues
Can rapidly synthesis or degrade proteins
Unlike other tissues, can also rapidly synthesise or degrade amino acids.

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5
Q

How many amino acids can be made in the body and how many are essential in the diet?

A

10 can be synthesised, 10 have to be taken in

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6
Q

How does transamination work (making amino acids?)

A

1) Precursor alpha-keto acid needed (eg. pyruvate)

2) Donor of amino group needed (commonly glutamic acid)

3) An aminotransferase enzyme catalyses reaction (like alanine transaminase or aspartate transaminase)

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7
Q

What promotes protein synthesis

A

Insulin and growth hormone

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8
Q

When there is tissue amino acid deficiency, where can amino acids be found?

A

The plasma proteins in the blood can be broken down.

Note that plasma proteins maintain oncotic pressure in blood as they hold water in the plasma

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9
Q

Liver disease can often lead to bleeding because…

A

Fewer clotting factors made from liver.

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10
Q

Vitamin K is fat-soluble and essential for the carboxylase enzyme needed to make clotting factors. What is needed for its digestion and absorption and what condition might prohibit this?

A

Bile, biliary obstruction. May cause bleeding as not making clotting factors.

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11
Q

In transamination, amino acids are converted to keto acids. What else is produced?

A

Glutamate

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12
Q

How is ammonium formed?

A

The glutamate produced from transamination has the amine group taken off, catalysed by glutamate dehydrogenase to from ammonia, then forms ammonium.

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13
Q

Where does the urea cycle take place?

A

Cytoplasm and mitochondria of hepatocytes.

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14
Q

What happens in the mitochondria of hepatocytes?

A

Ammonia reacts with ATP and CO2 to form citrulline from ornithine.

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