1
Q

Main functions of lipids

A

Formation and maintenance of cell membranes: phospholipid and cholesterol.

Energy storage: triglycerides.

Formation of hormones, vitamins and bile acids: steroids and fatty acids.

Electrical insulation in neurones.

Thermal insulation in adipose tissue.

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2
Q

Short term, labile energy sources

A

ATP

Redox agents: NAD, FAD

Ionic transmembrane gradients.

Creatine phosphate.

Though these are energy sources, they are not stable and do not last long.

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3
Q

Formation of fatty acids from glucose.

A

Glucose is broken down into acetyl-CoA during the link reaction of aerobic respiration.

Acetyl CoA is then converted to fatty acids using ATP.

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4
Q

Fatty acid synthesis from Acetyl CoA

A

This occurs in the cytosol in a great reducing environment:

Acetyl-CoA is used to make fatty acids using ATP, reducing power from electrons and fatty acid synthase.
Also produces CO2 and releases CoA.

2 carbons are added at a time to form fatty acids. Fatty acid chains are 16-20 carbons long with an even number of carbons.

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5
Q

Beta oxidation of fatty acids

A

The break down of fatty acids back to acetyl-CoA, which occurs in the mitochondria.

Fatty acid chain is shortened 2 carbon at a time to from acetyl-CoA and ATP.
Hence why fatty acids are storage for energy.

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6
Q

Fatty acids

A

Storage of energy: breaks down to release ATP in beta oxidation.

Structure: Hydrocarbon chain attached to carboxylic acid.
50 % of fatty acids are unsaturated- mono/polysaturates.

Forming double bonds is energy consuming so some fatty acids are essential, only obtained from diet.

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7
Q

Fat mobilisation

A

The breakdown of fatty acids to acteyl-CoA and ATP, 2 carbons at a time.

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8
Q

Triglycerides

A

Lipid molecule: contains even number of carbons, 16-20 carbons long.

Composed of 3 fatty acids attached to a glycerol molecule.

Cannot enter cells on its own, must be broken down before being transported.

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9
Q

Statins

A

Drugs that blocks the conversion of Acetyl-coA into cholesterol.

This treats hypercholesterolemia and reduces risk of coronary heart disease.

Blocks HMG-CoA reductase, the first enzyme used to make cholesterol.

Examples:
Simvastatin
Pravastatin

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10
Q

Carbohydrates in the brain

A

Glycogen cannot be stored in neurones, can only be stored in astrocytes.

Neurones get their energy source from ketone bodies.

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11
Q

Cholesterol

A

Vitamin D precursor

Either obtained from diet of made in the liver (very energy consuming).

Most of cholesterol (75%) in the plasma undergoes esterification.

Too much in the blood increases risk of coronary heart disease due to hypercholesterolemia.

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12
Q

Cholesterol esters

A

Made by reacting cholesterol with fatty acids, using LCAT enzyme.

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13
Q

Acetyl-CoA transport in plasma

A

Cannot be transported in plasma, has to be hydrolysed first

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14
Q

Ketone bodies

A

The following water soluble molecules:
Acetoacetate
Beta-hydroxybutyric acid
Acetone (one of the product of the breakdown of the previous ketone bodies)

They are a major source of energy that can last for 5 hours and are made from acetyl-CoA during fasting.

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15
Q

Diabetics and ketone bodies

A

Diabetic people do not utilise glucose as their cells are unresponsive.

This leads to energy being produced from the breakdown of ketone bodies. But ketone bodies only last 5 hours so if it is not used, it is wasted.

This can cause weight loss in diabetic people as food being eaten is not used for energy.

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16
Q

Acetone

A

A type of ketone body excreted by the kidneys.

17
Q

Unsaturated fatty acids

A

Contain C=C and make membrane more fluid due to the ‘kink’.

Fatty acids that are contain cis c=c are less flexible as they have an angle of 123 degrees.

This gives prevents them from packing more tightly and gives them a lower melting point than trans fats.

Trans fats have 132 degrees and look linear. They can pack more tightly.

18
Q

Exogenous lipid transport

A

Transporting lipid from the gut to the liver and periphery tissues,.

Fatty acids are absorbed in the small intestines and packaged into chylomicrons.

The liver and peripheries, like adipose and muscle tissue, take up chylomicrons and increase the concentration of lipids in the plasma.

19
Q

Endogenous lipid transport

A

Transporting lipid from the liver to periphery tissue.

Liver packages lipids in very low density lipoproteins (VLDL) and transports to adipose and muscle tissue.

20
Q

Reverse cholesterol lipid transport

A

Transporting lipid from periphery to the liver. This indicates that lipid levels are low.

Lipids are packaged into high density lipoproteins which are taken up by the liver.

21
Q

Bile production- lipid transport

A

Method of transporting lipid from the liver to the gut.

Bile is released from the liver and gallbladder into the cystic duct in the duodenum, in the small intestines.

Bile emulsifies fats in the intestines, facilitating its absorption.

22
Q

Very low density lipoprotein. (VLDL)

A

Transports cholesterol and triglycerides from the liver to the muscle and adipose tissue- Endogenous transport.

After the triglycerides are released then VLDL becomes intermediate density lipoprotein (IDL).

23
Q

High density lipoprotein (HDL)

A

Transports lipids from periphery to the liver.

High concentrations reduces the risk of developing cardiovascular diseases.

High density- smaller amount of lipids carried as there are more particles per given area compared to LDL and VLDL.

High levels in the blood indicate that cholesterol is being recycled.

24
Q

What happens during starvation

A

Lack of glucose present leads to the increase of ketogenesis:

Excess beta oxidation occurs which produces excess acteyl-CoA

Too much acetyl-CoA being produced compared to its use in the Kreb’s cycle.

25
Q

Lipoproteins

A

Soluble structures that store lipids.

Contains apolipoproteins which carries lipids, like apoE.

26
Q

Chylomicrons

A

Lipoproteins that carry exogenous lipids to the liver and periphery- exogenous transport.

27
Q

Hypercholesterolaemia

A

High fasting levels of plasma cholesterol.

This increases the risk of atherosclerosis.

Influenced by environmental (consuming too much cholesterol) and genetic factors.

28
Q

Lipoprotein protease

A

Enzyme that breaks down triglycerides into fatty acids and glycerol.

Located in the cell membrane of capillary walls.

Allows TG to be moved into cell as it cannot be transported in plasma.