Drive - proteins synthesis and degredation Flashcards

1
Q

Where are the majority of proteins produced by the made?

A

The liver

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2
Q

What are the 4 Starling Forces?

A

Capillary hydrostatic pressure

Interstitial hydrostatic pressure

Osmotic force due to plasma protein concentration

Osmotic force due to intestinal fluid protein concentration

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3
Q

What direction of movement does capillary hydrostatic pressure favour?

A

Fluid movement out of the capillary

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4
Q

What direction of movement does interstitial hydrostatic pressure favour?

A

Fluid movement into the capillary

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5
Q

What direction of movement does the osmotic force due to plasma protein concentration favour?

A

Fluid movement into the capillary

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6
Q

What direction of movement does the osmotic force due to intestinal fluid protein concentration favour?

A

Fluid movement out of the capillary

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7
Q

With reference to Starling Forces what happens to fluid at the arterial end of the capillaries?

A

Bulk filtration out of the capillary

Due to high capillary hydrostatic pressure and low interstitial hydrostatic fluid pressure

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8
Q

Why is their a bulk absorption of fluid into the capillaries at the venous end?

A

As capillary hydrostatic pressure has decreased due to resistance encountered as blood flows through the capillary wall

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9
Q

Why can liver failure cause oedema?

A

Liver is needed to produce albumin.

Albumin is needed to maintain capillary oncotic pressure

Therefore decrease in albumin means less water reabsorbed.

Accumulation of water in the interstitial fluid

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10
Q

What is protein turnover?

A

The continuous degradation and re-synthesis of all cellular proteins

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11
Q

List 3 causes of increased rate of protein turnover

A

Tissue damage

Uterine tissue in pregnancy

Skeletal muscle during starvation

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12
Q

What are the 2 primary methods of protein break down?

A

Lysosomal and Ubiquitin proteasome pathway

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13
Q

What is lysosomal breakdown of proteins carried out by? (both general and specific)

A

The reticulo-endothelial system in the liver.

Specifically the sinusoidal endothelial cells, Kupffer cells and pit cells

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14
Q

What is the role of sinusoidal endothelial cells in protein degradation?

A

Remove soluble proteins and fragment from the blood (through fenestrations). Where they are the fused into lysosomes and hydrolysed

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15
Q

What is the role of Kupffer cells in protein degradation?

A

Phagocytose particulate matter into phagosomes before hydrolysation occurs

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16
Q

What are Kupffer cells?

A

Livers resident macrophages

17
Q

Where does the ubiquitin-protease pathway occur?

A

In the cytoplasm of cells

18
Q

What is the role of the ubiquitin-protease pathway?

A

To degrade protein by unfolding it and breaks it down into small peptides.

It preferentially degrades denatured (unfolded) proteins that are defective

19
Q

Where does amino acid degradation and catabolism occur?

A

In the hepatocytes of the liver

20
Q

What is catabolism?

A

The break down of complex substances to simpler ones accompanied by the release of energy

21
Q

What are the 2 main amino acid catabolism processes?

A

Oxidative deamination and transamination

22
Q

What occurs in oxidative deamination?

A

Production of free ammonia (from amino group) and alpha-keto acid (which is then used in the Krebs cycle)

23
Q

What enzymes is need for the catalysis of oxidative deamination?

A

Glutamate dehydrogenase

24
Q

What is the problem with excess NH3 in oxidative deamination?

A

The process of oxidative deamination is reversible. Excess ammonia crosses blood-brain barrier and reacts with alpha-ketoglutarate (which causes a decrease in ATP levels)

25
Q

What occurs in transamination?

A

Transfer of an alpha-amino group from amino acid to a keto-acid to form an alpha-keto-acid

26
Q

What enzyme is involved in transamination? and where is this found?

A

Aminotransferase = found in the cytosol of the mitochondria throughout the body particularly those of the liver and kidneys