Kidney Disease and the Urea Cycle Flashcards

1
Q

What is haemodialysis?

A

It is a life-saving treatment for kidney failure that uses a machine to filter and clean the blood, removing waste products and excess fluid when the kidneys are unable to so effectively.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Where is urea produced?

A

In the liver, in the urea cycle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the major nitrogenous excretory product?

A

Urea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What does the urea cycle do?

A

detoxifies the ammonia (NH4+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the amount of ammonia in the blood?

A

30 to 60 umol/L

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Explain nitrogen balance

A

The amount of nitrogen ingested is balanced by the excretion of an equivalent amount of nitrogen. About 80% of excreted nitrogen is in
the form of urea.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Ammonia originates in the catabolism of amino acids that are primarily produced by the degradation of proteins – dietary as well as
existing within the cell:

A
  • digestive enzymes
  • proteins released by digestion of cells sloughed-off
    the walls of the GIT
  • muscle proteins
  • haemoglobin
  • intracellular proteins (damaged, unnecessary)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Why does ammonia is toxic, especially for the CNS?

A

Because it reacts with a-ketoglutarate, thus making it limiting for the TCA cycle = decreased in ATP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Liver damage or metabolic disorders associated
with elevated ammonia can lead to:

A

tremor, slurred speech, blurred vision, coma and death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Explain Nitrogen removal from amino acids processes:

A
  1. Remove amino group
  2. Take amino group to liver for nitrogen excretion
  3. Entry into mitochondria
  4. Prepare nitrogen to enter urea cycle
  5. Urea cycle
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Name the nitrogen carriers:

A
  1. Glutamate
  2. Glutamine
  3. Alanine
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Explain Creatinine:

A

Produced from creatine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Explain urea cycle disorders:

A

Urea cycle disorders (UCDs) include a variety of genetic defects in ammonia metabolism in which one of the urea-synthesis passages is defective, leading to hyperammonemia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly