24. Nitrogen Excretion Flashcards

1
Q

What is nitrogen excretion dependent on?

A

Protein intake
Protein synthesis
Protein breakdown
Renal function

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2
Q

What are the stages of amino acid catabolism?

A

Transamination
Oxidative deamination
Urea cycle

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3
Q

What are the products of transamination?

A

Alpha-keto acid

Glutamate

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4
Q

What are the products of oxidative deamination of glutamate?

A

Ammonia

Alpha-ketoglutarate

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5
Q

What is transamination?

A

Amino portion of one amino acid is transferred to a keto acid

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6
Q

What enzyme carries out oxidative deamination?

A

Glutamate dehydrogenase

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7
Q

What is the purpose of the urea cycle?

A

NH3 is converted to safe form for excretion

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8
Q

Where does the urea cycle take place?

A

Cytosol and mitochondria of liver

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9
Q

What are the steps in the urea cycle?

A
  1. NH3 + CO2 + 2ATP= Carbamoyl phosphate + 2ATP + P
    (carbamoyl phosphate synthetase 1)
  2. Carbamoyl group transferred from carbamoyl phosphate to ornithine to create citrulline
    (Ornithine transcarbamoylase)
    Citrulline released into the cytosol
  3. Citrulline + ATP + aspartate= argininosuccinate + AMP + PPi
    (Argininosuccinate synthetase)
  4. Argininosuccinate cleaved to form fumarate and arginine
    (Argininosuccinate lipase)
  5. Arginine is hydrolysed to urea and ornithine
    (Arginase)
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10
Q

What drives urea transport in the nephron?

A

Passive diffusion

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11
Q

What does the amount of urea present in the urine depend on?

A

ADH

-promotes expression of UT-A urea transporters in the collecting duct

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12
Q

What are the nitrogenous components of urine?

A

Urea
Creatinine
Uric Acid
Ammonia

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13
Q

What is the main role of creatinine in the body?

A

Facilitates ATP production in energy dependent tissues

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14
Q

Where and from what is creatine made?

A

Liver

Arginine

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15
Q

Where is creatine phosphorylated?

A

Muscle

Brain

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16
Q

What is creatinine formed from?

A

Created spontaneously from phosphocreatine

17
Q

What does plasma levels of creatinine depend on?

A

Muscle bulk

18
Q

What is uric acid?

A

End product of purine metabolism

19
Q

What causes hyperuricaemia?

A

High purine intake

Poor renal handling

20
Q

What does hyperuricaemia lead to?

A

Gout

Kidney stones

21
Q

Where and by what is ammonia produced intrarenally?

A

Glutamate metabolism

PCT

22
Q

What can increase levels of ammonia?

A

Liver disease
Diet
UTIs

23
Q

What does urine volume depend on?

A
Fluid intake
Fluid loss
Hormones
Osmotically active substances in tubular fluid
Drugs
Pathological conditions
24
Q

What can cause urine to have an unusual colour?

A

Dehydration
Medication
Disease
Diet

25
What can cause urine to be cloudy?
Mucous, sperm, prostatic fluid | Blood cells, bacteria
26
What is urine sediment?
Urine that has been centrifuged to concentrate the substances
27
What are Hyaline casts?
Cylindrical particles made of coagulated protein released by tubule cells (Tamm-Horsfall mucoprotein) Substances can become trapped in cast in disease
28
What could cause the formation of crystals in urine?
pH change | Concentrations increase
29
How is proteinuria diagnosed?
Foamy urine | Dipstick test
30
What are the 3 main mechanisms that cause proteinuria?
Glomerular Overload/prerenal Tubular
31
What is glomerular proteinuria?
Caused by disease in the glomerulus eg. diabetic nephropathy Excess proteins filtered into urine
32
What is Overload/ Prerenal proteinuria?
Presence of excess amounts of filterable, low Mr proteins | Eg. Amylase in acute pancreatitis
33
What is tubular proteinuria?
Low reabsorption of filtered proteins in the PCT | Eg. Fanconi syndrome