Fats and Proteins Flashcards

1
Q

What can you use glycerol for?

A

Gluconeogenesis

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1
Q

What is the precursor molecule for ketone production?

A

Acetyl-CoA

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2
Q

What part of fat molecules are made into ketones?

A

FAs

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2
Q

Which tissues don’t use fat as fuel?

A

Brain

RBCs

Testes

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2
Q

Are free amino acid supplements like tryptophan good?

A

No!

Eg. Tryptophan supplements caused eosinophilia myalgia syndrome

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3
Q

What are the four D’s of Pellagra?

A

photosensitive dermatitis, diarrhea, dementia, and death

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4
Q

What is the recommended daily intake of protein in Australia?

A

1g/kg

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4
Q

In term of weight, how much of a 70kg man is protein?

A

12kg

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4
Q

What amino acid does corn lack? Why is it important?

A

Tryptophan > niacin deficiency > Pellagra

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6
Q

How much protein do we make and break down per day?

A

300g

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7
Q

What happens if the concentration of FAs in the blood exceeds the carrying capacity of albumin?

A

The heart can be affected on exertion - cardiac arrhythmias

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8
Q

In what form are fats stored?

A

Triacylglycerol

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9
Q

Oxaloacetate can be made from which aa?

A

Aspartate

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11
Q

Do adipocytes have a cytoskeleton?

A

No

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12
Q

Ketone bodies are a mixture of what?

A

acetoacetate

β-hydroxybutyrate

acetone

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12
Q

What type of acids are ketones?

A

Strong

Organic

13
Q

What is the first source of substrate for gluconeogenesis during starvation?

A

Proteins from muscle

15
Q

What is beta-oxidation?

A

The process by which FAs are broken doing into acetyl-CoA in the mitochondria

16
Q

Why is omega 3 beneficial?

A

They promote prostacyclin production - antithrombogenic

They downregulate thromboxane production (they are thrombogenic)

18
Q

What do branch chain amino acids do in muscles?

A

Transaminate

19
Q

Pyruvate can be made from which aa?

A

Alanine

21
Q

How much energy does oxidation of fats yield?

A

37kJ/g

22
Q

What type of cells take up fat?

A

Adipocytes

Myocytes

22
Q

What causes Pellagra?

A

Niacin and tryptophan deficiency

24
Q

What does omega 3 provide?

A

EPA - a long chain FA that we are unable to make

25
Q

What are the three outcomes of aa’s absorbed in the gut?

A

Protein production for liver, muscles, gut and others

Neurotransmitters and haem

Used as carbon in the TCA cycle for production of glucose, fat or ketones

26
Q

What happens to the 16g of N that the average Australian consumes per day?

A

15g are excreted in urine

1g is excreted in faeces

28
Q

What are the names of the branch chain amino acids?

A

Valine

Leucine

Isoleucine

29
Q

T/F Chylomicrons can travel in the lymph

A

True

30
Q

Are proteins ketogenic or glucogenic?

A

Both

31
Q

How much ATP is produced by beta-oxidation?

A

106

32
Q

What is the function of the alanine cycle?

A

Shuttle excess N from muscles to the liver or kidneys

33
Q

What is the major cause of long term damage as a result of starvation?

A

Thiamine deficiency after 2 weeks

34
Q

Which aa acts as a N sink?

A

Glutamate

35
Q

Alpha-ketoglutarate can be made from which aa?

A

Glutamate

36
Q

How are fats transported around the body?

A

In chylomicrons

37
Q

What does carnitine do?

A

Transports FAs into the mitochondria for beta-oxidation