Energy Prodcution - Lipids Flashcards

1
Q

What are the three classes of lipids?

A
  • Fatty acids derivatives - fatty acids + TAGS
  • **Hyroxy-methyl-glutaric acid derivates* - ketone bodies
  • Vitamins - A,D,E,K
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2
Q

What are the lipid fuel molecules?

A

Fatty acids
TAGs
Ketone bodies

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3
Q

Are carbs or lipids more reduced?
What does this mean

A

Lipids are more reduced than carbs
Release more energy when oxidised
Complete oxidation requires O2

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4
Q

Compare and contrast the energy storage of TAGs in a healthy and obese man?

A

Healthy:
15 kg > 600,000kJ energy content

Obese:
80kg > 3,000,000kJ energy content

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5
Q

Describe the storage of TAGs

A

Stored in anhydrous form
Stored in adipose tissue
Under hormonal control

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6
Q

When are TAGs broken down?

A

Low blood glucose;
- Prolonged exercise
- Starvation
- Pregnancy

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7
Q

Outline the metabolism of TAGs and the tissues involved

A

GI tract:
TAGs <> glycerol + fatty acids

Blood:
Glycerol > glycerol
Fatty acids > chylomicrons (packaged into lipoprotein)

Tissues
Glycerol > liver
Chylomicrons > adipose > released as fatty acids into blood > to muscles

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8
Q

How are fatty acids carried to tissues?

A

Bound to albumin
Albumin-fatty acid complex

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9
Q

Describe what happens in TAG metabolism after absorption in the GI tract

A

1- convert back to triglycerides in the GI trac
2- packed into lipoprotein particle > Chylomicron
3- released into blood via lymphatics
4- carried to adipose
5- store as triglyceride

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10
Q

What is fat mobilisation controlled by?

A

Hormone sensitive lipase

Increases with glucagon + adrenaline
Decreases with insulin

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11
Q

Where are fatty acids not found?

A

Brain - cant cross blood brain barrier
Cells without mitochondria - *e.g. RBCs**

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12
Q

Outline the steps in triglyceride/fatty acid cycle in adipose

A

1- glucose transport
2- glycolysis
3- esterification
4- lysis
5- re-esterification

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13
Q

Describe beta oxidation

A

Fatty acid catabolism
Removal of 2C units from FA to generate acetyl coA

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14
Q

Describe fatty acid activation

A

Fatty acid + coA > fatty acyl co A
fatty acyl coA synthase
Transported across mitochondria membrane via carnitine shuttle

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15
Q

Describe the carnitine shuttle

A

Transports fatty acyl CoA across mitochondrial membrane
CAT1+2 - carnitine acyl transferases

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16
Q

What inhibits the carnitine shuttle?

A

Malonyl CoA

17
Q

Identify three features of beta oxidation

A

H+ and e- transferred to NAD+ and FAD
Stops in the absence of O2
No ATP synthesis

18
Q

Outline glycerol metabolism

A

In the liver
TAG synthesis
^
Glycerol > glycerol phosphate > DHAP > glycolysis
glycerol kinase

19
Q

Function of acetyl CoA

A

Most important intermediate in catabolic and anabolic pathways

20
Q

What are the three ketone bodies produced?

A

Acetone/acetate
Acetoacetate
B-hydroxybutyrate

21
Q

What is the normal plasma conc of ketone bodies?

A

<1mM

22
Q

Ketone bodies conc. in starvation

A

2-10mM - physiological ketosis

23
Q

Ketone bods conc. in untreated type1 diabetes

A

> 10nM - pathological ketosis

24
Q

Outline ketone bodies synthesis

A

By liver mitochondria

                   Mevalonate > cholesterol 
                          ^ *HMG-CoA reductase*  
                          |

Acteyl coA > HMG-CoA > acetoacetate >acetone or B hydroxybutyrate
synthase lyase

25
Q

How is acetone formed?

A

The spontaneous decarboxylation of acetoacetate

26
Q

Explain how ketone bodies synthesis is regulated by insulin:glucagon ratio in fed and starved states

A

Fed state:
High insulin:glucagon ratio
Inhibits lyase
Activates HMG CoA reductase
Increased cholesterol synthesis
Decreased KB synthesis

Starved state
Low insulin:glucagon ratio
Activates lyase
Inhibits HMG CoA reductase
Decreases cholesterol synthesis
Increases KB synthesis

27
Q

How are ketone bodies removed from the body?

A

When above renal threshold
Excreted in urine > ketonuria

28
Q

How is acetone excrete from the body?

A

Via a lungs > smell of acetone on breath