Metabolism Flashcards

(29 cards)

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?

19
Q

What produces F 2,6, P?

20
Q

What is the final product of glycolysis?

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?

24
Q

What apoprotein is present on the LDL?

25
What enzymes esterifies cholesterol so it can be transported?
LCAT enzyme
26
What is the average energy values of the fats, carbohydrates and protein?
Fat: 9 calories/ gram Carbohydrate: 4 calories/ gram Protein: 4 calories/ gram *note that fat is double than the other two.
27
What would be a diagnosis of server malnutrition?
> 3 standard deviations for median height and weight Notable wasting Nutritional oedema
28
What would be the diagnosis of moderate malnutrition?
2-3 standard deviations for median height and weight
29
What would the diagnosis of mild malnutrition be?
1-2 standard deviations below.