Session 2 Lecture 2 Flashcards

(68 cards)

1
Q

Are lipids soluble or insoluble?

A

Insoluble in water (hydrophobic) but are soluble in organic solvents

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2
Q

How many classes of lipids are there?

A

3

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3
Q

What are the different classes of lipids?

A
  • Fatty acid derivatives
  • Hydroxyproline-methyl glutaric acid derivatives
  • Vitamines
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4
Q

Give some examples of fatty acid derivatives

A

Fatty acids
Triacylglycerides
Phospholipids
Eicosanoids

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5
Q

What are fatty acids?

A

Fuel molecules

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6
Q

What are triacylglyerols?

A

Fuel storage and insulation

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7
Q

What are phospholipid function?

A

Component of membrane and plasma lipoproteins

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8
Q

What is eicosanoids function?

A

Local mediators

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9
Q

Give some examples of hydroxyl-methyl acid derivatives

A

Ketone bodies
Cholesterol
Cholesterol esters
Bile acids and salts

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10
Q

What are ketone bodies?

A

Water soluble fuel molecules

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11
Q

What is function of cholesterol?

A

Membrane and steroid hormone synthesis

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12
Q

What is the function of cholesterol esters?

A

Cholesterol storage

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13
Q

What is the function of bile acids and salts?

A

Lipid digestion

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14
Q

What is the major dietary and storage lipid in the body?

A

Triacylglycerols

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15
Q

What is the structure of a triacylglycerol?

A

3 fatty acids esterified to glycerol

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16
Q

Describe some features of triacylglycerols?

A

Triacylglycerols are hydrophobic therefore stored in an anhydrous form.

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17
Q

How are TAGs stored?

A

Adipose tissue

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18
Q

When are TAGs used?

A

Utilised in prolonged exercise, starvation and during pregnancy

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19
Q

What sort of control is the storage of TAGs under?

A

Hormonal control

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20
Q

What is the storage of TAGs promoted by?

A

Insulin

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21
Q

What is storage of TAGs reduced by?

A

Glucagon, adrenaline, cortisol, growth hormone and thyroxine.

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22
Q

What happens when you ingest lipids?

A

The lipid is hydrolysed by pancreatic lipase in the small intestine to glycerol and fatty acids

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23
Q

What does the hydrolysation of lipids require?

A

Bile salts and a protein factor called colipase

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24
Q

What happens to the glycerol from the lipid breakdown?

A

Glycerol enters the blood stream and is transported to the liver where it is metabolised

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25
Describe some features of fatty acids?
They are hydrophobic and highly reduced molecules, properties that make them ideal for energy storage
26
Are saturated fatty acids non essential components of the diet?
Yes because they can be synthesised from carbohydrates and certain amino acids
27
Why are certain polyunsaturated fatty acids essential components of the diet?
They can't be synthesised in the body
28
Give a n example of an important polyunsaturated fatty acid?
Arachidonic acid - it is a starting point for the synthesis of the eicosanoids
29
What are the eicosanoids?
They are a family of signalling molecules in the body, including prostaglandins
30
What happens to some of the fatty acids and glycerol in the small intestine?
Some is recombined and transported as TAG by chylomicrons and stored as adipose tissue
31
What activated fat metabolism?
Stressful situations - aerobic exercise, starvation, lactation. Adrenaline, glucagon, GH, cortisol and thyroxine
32
What inhibits fat metabolism?
Insulin
33
What is the first stage in fat metabolism?
Adipose tissue TAG are hydrolysed by the enzyme hormone-sensitive lipase to release fatty acids and glycerol
34
What is the first stage of fat metabolism called?
Lipolysis
35
How are fatty acids carried to tissues?
This is done via the blood stream bound non-cavelently to albumin
36
What are albumin bound fatty acids known as?
Non-esterified fatty acids (NEFA) or free fatty acids (FFA)
37
What happens to glycerol in the liver?
It may be oxidised, converted to glucose or used in the synthesis of TAGs
38
What is Beta-oxidation?
The process by which fatty acids are oxidised to release energy
39
Where does beta-oxidation occur?
Mitochondria
40
Why does beta-oxidation not occur in cells of the central nervous system?
Fatty acids do not readily cross the blood-brain barrier
41
What needs to happen before fatty acids oxidised?
They have to be activated
42
How are fatty acids activated?
Link the fatty acids to coenzyme
43
What is required for the activation of fatty acid?
ATP and is catalysed by fatty acyl coA synthase
44
Where does the activation of fatty acids occur?
Outside of the mitochondrion
45
How does the activated fatty acid cross the inner mitochondrial membrane?
Carnitine shuttle
46
What inhibits the transport of activated fatty acids?
Malonyl coA - an intermediate in the synthesis of fatty acids
47
What happens if someone suffers from a defective micotchondiral fatty acid transport system?
They suffer from poor exercise tolerance and have usually large amounts of TAGs in their muscle cells therefore get lipid droplets in muscle
48
What happens overall in beta-oxidation of fatty acids?
Oxidised the fatty acid and removes a C2 unit. The shortening fatty acid is cycled through the reaction sequence repeatedly removing a C2 unit each turn until only 2 carbon atoms remain
49
What does the reaction sequence for beta-oxidation require?
Mitochondrial NAD+ and FAD and can;t occur in the absence of oxygen.
50
Is ATP synthesised in b-oxidation
No direct synthesis
51
What is special about all the intermediates in the pathway?
They are linked to coA and the C atoms of the fatty acid are converted to acetyl coA
52
Which process derives more energy - FA oxidation or glucose oxidation?
Fatty acid oxidation
53
What is the main convergence point for catabolic pathways?
Acetyl coA
54
How many different ketone bodies are produced in the body?
3
55
What are the different ketone bodies produced in the body?
Acetoacetate, acetone and b-hydroxybutyrate
56
Where is acetoacetate synthesise?
Liver from acetyl coA
57
Where is b-hydroxybutyrate synthesised and where from?
Liver from acely coA
58
How is acetone synthesised?
Arises from spontaneous (non-enzymatic)
59
When can the concentration of ketone bodies increase?
Increases in starvation and untreated type 1 diabetes
60
Where are ketone bodies synthesised?
Liver mitochondria
61
What enzymes are responsible for synthesis of ketone bodies in the liver?
Lyase and reductase enzymes
62
What controls the lyase and reductase enzymes?
Controlled by the insulin/glucagon ration
63
What happens when the insulin/glucagon ration falls?
Lyase is activated and reductive is inhibited and ketone body formation is activated
64
What happens when the insulin/glucagon ratio increases?
The lyase is inhibited and the reductive is activated and cholesterol synthesis occurs
65
What does the synthesis of ketone bodies require?
Fatty acids to be available for oxidation in the liver following excessive lipolysis in adipose tissue. The plasma insulin/glucagon ratio to be low, usually due to a fall in plasma insulin
66
Ketone body function?
Important fuel molecules that can be used by all tissues containing mitochondria including the CNS
67
What happens if acetoacetate and b-hydroxybutyrate are present in high concentrations?
They may cause acidosis (ketoacidosis)
68
Why do you get the characteristic smell of acetone on someone's breath if they have untreated type 1 diabetes?
Acetone is a volatile substance that may be excreted via the lungs