Metabolism Flashcards

1
Q

What are the FIVE complexes of the Electron transport chain?

A
Complex I:  NADH - Q - Oxidasereductase 
Complex II : FADH - Q - Reductase 
Complex III: Q  Cytochrome C - Reductase 
Complex IV: Cytochrome C- Oxidase 
ATP Synthase
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2
Q

When Triglycerdies are broken down by lipases during fasting, what is released?

A

Glycerol and 3 fatty acid chains

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3
Q

What happens to Glycerol during fasting?

A

In the liver it is converted to dihydroacetone phosphate and therefore can enter the glycolysis or gluneogensis

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4
Q

What happens to the fatty acids during fasting?

A

In the liver undergo Beta-oxidation to produce NADH & FADH and Acetly Co-A.

Acetly co - A can either enter the krebs cycle or be converted into ketone bodies and released into the blood.

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5
Q

For large chained fatty acids to enter the matrix of the mitrochondria, what must occur?

A

Addition of a Co-A group to form: Acyl co-A

Once in the outer membrane space, the Acyl Co-A is removed and carnitine is added to allow it pass through the inner membrane.

after which Acyl - Co -A is added again

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6
Q

What is process by which the Acly - coA moves into the mitrochondrial matrix?

A

Carnitine shuttle

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7
Q

What enzyme adds a carnitine?

A

Palmtoyiltransferase

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8
Q

What is produced through the krebs cycle of one glucose molecule?

A

3x NADH2 (2x)

FADH (x2)

ATP (x2)

2x CO2 (x2)

*remember always multiplying by two as there is two krebs cycles happening for every glucose molecule

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9
Q

During starvation, amino acids may be broken down and used as energy. It order to do this, what must be broken off and what is this process called?

A

The amine group must be broken off to expose the carbon backbone.

Transamination

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10
Q

What acceptor molecule is usually used during transamination and what does it become?

A

Alpha - Keto - glutarate

Glutamate

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11
Q

What is the fate of glutamate?

A

In the liver broken down to amonia and secreted as urea

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12
Q

How are fatty acids transported around the blood?

A

Albumin complex

Lipoproteins

Chlymicrons

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13
Q

How long can an average 70Kg person survive without food for and what is the break down of energy sources used?

A

98 days
fat = 3 months
Protein = 14 days

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14
Q

If a sprinter is training, doing short burst of intense anaerobic exercise, what will cause fatigue?

A

Lack of phosphocreatine

Hydrogen proton accumulation

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15
Q

How many ATP molecules are made from one Glucose molecule?

A

It is thought 38, although the answer is probably closer to 30.

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16
Q

What are the important enzymes during glycolysis?

A

Hexokinase/ Glucokinase
PFK -1 (and 2)
Pyruvate Kinase

17
Q

What will inhibit the activity of PFK-1?

A

^ATP, ^Citrate

Decreased AMP.

18
Q

What is a powerful stimulation to PFK-1?

A

F 2,6, P

19
Q

What produces F 2,6, P?

A

PKF-2

20
Q

What is the final product of glycolysis?

A

pyruvate

21
Q

What are the products of GlyColysis?

A
4 ATP (NET of 2) - remember 2 were invested before 
2 NADH
22
Q

Where is ATP made in the glycolysis?

A

1,3 Bisphosphoglycerate > 3 Phosphoglycerate

Phosphenolpyruvate > pyruvate

23
Q

What apoprotein is present on the vLDL and chylmicrons?

A

ApoB

24
Q

What apoprotein is present on the LDL?

A

ApoA

25
Q

What enzymes esterifies cholesterol so it can be transported?

A

LCAT enzyme

26
Q

What is the average energy values of the fats, carbohydrates and protein?

A

Fat: 9 calories/ gram
Carbohydrate: 4 calories/ gram
Protein: 4 calories/ gram

*note that fat is double than the other two.

27
Q

What would be a diagnosis of server malnutrition?

A

> 3 standard deviations for median height and weight

Notable wasting

Nutritional oedema

28
Q

What would be the diagnosis of moderate malnutrition?

A

2-3 standard deviations for median height and weight

29
Q

What would the diagnosis of mild malnutrition be?

A

1-2 standard deviations below.