Metabolism and regulation Flashcards

1
Q

In the post-absorptive state what are the 3 main sources of glucose?

A

Glycogenolysis
Lipolysis
Protein breakdown

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2
Q

Where does glycogenolysis occur?

A

In the liver (directly) and in skeletal muscle (indirectly)

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3
Q

What is the mechanism involved in hepatic glycogenolysis?

A

Enzymatic conversion of glycogen to glucose

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4
Q

How does skeletal muscle indirectly produce glucose?

A

Glucose-6-phophate  ATP, pyruvate and lactate. Lactate then processed by the liver which releases glucose into the blood (which can then be used)

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5
Q

How does lipolysis produce glucose?

A

Hydrolysis of triglycerides produce glycerol and fatty acids. Glycerol is converted enzymatically to glucose the liver.

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6
Q

How can protein break down produce glucose?

A

Amino acids converted by the alpha-keto acid to glucose in the liver

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7
Q

Define gluconeogenesis

A

The process of generating new molecules of glucose from non-carbohydrate sources

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8
Q

How is fat stored?

A

Within adipocytes which then form tissue called adipose tissue

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9
Q

What % of all energy stored in the body do triglycerides account for?

A

78%

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10
Q

Name 3 main functions of lipids

A

Energy reserves
Structural part of cell membranes
Hormone metabolism

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11
Q

Where are high density lipoproteins formed?

A

Liver

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12
Q

Where are low density lipoproteins formed?

A

Plasma

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13
Q

What is the main function of high density lipoproteins?

A

To remove excess cholesterol from the blood and tissue

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14
Q

What is the main function of low density lipoproteins?

A

To transport cholesterol to cells throughout the body.

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15
Q

A positive net gain in amino acids is called …

A

Anabolic

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16
Q

A negative net gain in amino acids is called …

A

Catabolic

17
Q

What is the most common cause of a positive nitrogen balance?

A

Pregnancy

18
Q

What is the most common cause of a negative nitrogen balance?

A

Malnutrition

19
Q

Where and by what process is alanine converted to pyruvate?

A

Transamination occurs in the liver

20
Q

What is produced when glutamate undergoes oxidative deamination?

A

Ammonium (NH4+) which quickly dissociates into ammonia (NH3)

21
Q

Where are the enzymes utilised in the urea cycle found?

A

Cytosol of hepatocytes or the mitochondria (in the liver)

22
Q

What is arginine cleaved by arginase to produce?

A

Urea and ornithine

23
Q

Outline the urea cycle (provide key enzymes and substrates)

A

Arginine (+ arginase)  >urea and ornithine.
Ornithine (+NH3 +CO2) > citrulline
Citrulline (+ammonia)  >arginine

24
Q

What happens if the urea cycle does not occur (/not at a sufficient rate)?

A

High levels of ammonia in the blood

25
Q

What is the problem of high levels of ammonia in the blood?

A

Ammonia is neurotoxic (prevents the Krebs cycle occurring)

26
Q

Describe the action of lipoprotein lipase:

A

Breakdown of triglycerides (found in lipoprotein) into 2 free fatty acid and a monoglyceride.

27
Q

Describe the action of hepatic lipase:

A

Conversion of IDL to LDL.

28
Q

Where is bile secreted?

A

Liver

29
Q

Describe the role of bile:

A

To emulsify fats

30
Q

Where is bile stored and concentrated?

A

The gall bladder