Lipids Flashcards

(44 cards)

1
Q

Biological functions of lipids

A

Stored form of energy, steroid hormones, signalling molecules, structural element of membranes

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2
Q

Lipid classes

A

Fatty acids, triacylglycerol, phospholipids, glycolipid, steroids

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3
Q

Unsaturated fatty acids

A

One or more double bonds that kink hydrocarbon chain

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4
Q

Saturated fatty acids

A

Solid, no double bonds

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5
Q

Naming fatty acids

A

Number of carbons, place of double bond, number of double bonds present

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6
Q

Good fats

A

High in polyunsaturated fats eg olive oil sunflower oil

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7
Q

Bad fats

A

High in saturated fats eg beef

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8
Q

Really bad fats

A

Trans fatty acids (result from hydrogenation of vegetable oil) eg hard margarine

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9
Q

Humans cannot ingest double bonds beyond carbon

A

9

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10
Q

Omega 3 fatty acids

A

Derived from linolenic acids as essential fatty acids. Lower cholesterol levels, prevents obesity, reduces inflammation. Found in fish

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11
Q

Omega 6 FA

A

found in linoleic. Does not have benefits

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12
Q

Essential fatty acid deficiency

A

Depression, ADHD, scaly dermatitis etc

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13
Q

Triacylglycerols

A

Esters (neutral uncharged lipids) of fatty acids and glycerol. Major lipid component of adipose tissue. Dietary fuel and insulation

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14
Q

Phospholipids

A

2 fatty acids and phosphate group, amphipathic, in membrane, help with digestion as they are emulsifiers

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15
Q

What affects the melting points of fatty acids

A

Number of carbons and degree of unsaturation

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16
Q

Are lipids water soluble

A

No

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17
Q

What is the main dietary lipid

A

Triacylglycerol

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18
Q

How are lipids digested

A

In small intestine. Use of pancreatic enzymes. Promoted by emulsification (dispersion) by bile salts and peristalsis

19
Q

Bile salts

A

Biological detergents that form emulsions and mixed micelles, saves lipids coalescing in an aqueous environment. Derivatives of cholesterol

20
Q

How are triacylglycerols digested

A

Degraded by lipases to monoacylglycerol and fatty acids

21
Q

Cholesterol esters are broken down into

A

Cholesterol and free fatty acid by pancreatic cholesterol esterase

22
Q

What do products if lipid digestion form and where do they go

A

Form mixed micelles with bile salts and then approach brush border membranes of enterocytes and release lipid products that enter by diffusion . Only long chain FA need micelles

23
Q

Gall bladder secretes

24
Q

Chylomicrons

A

Intestinal cells that are packaged with apoB-48 which is a solubilising protein. They are then exported from small intestine by exocytosis into lymph then blood

25
What happens once chylomicrons reach tissue
- free FA used for energy or reesterified for storage - if depleted of triacylglycerols they go to liver (chylomicrons remnants) - lipoprotein lipase found in capillaries of muscle, adipose and skeletal tissue hydrolyse the TAG to fatty acids and glycerol
26
How are fatty acids release from storage in adipose tissue
By hormone sensitive lipase when it is activated phosphorylation in response to high epinephrine levels
27
What stops fatty acids from being released from TAG in adipose tissue
When plasma glucose and insulin levels are high and they promote dephosphorylation of lipase
28
Fatty acids are transported in blood by
Serum albumin ( plasma protein with 2-7 binding sites for FA)
29
If fatty acids are esterified how are they carried in blood
Lipoproteins
30
Beta oxidation pathway
Degrades fatty acids two carbons at a time and occurs in mitochrondrial matrix. Produces acetyl CoA and NADH and FADH2
31
Stages of beta oxidation
Activation of fatty acids in cytosol, transport into mitochondria by carnitine shuttle, degradation to two carbon fragments in the mitochondrial matrix- energy!
32
Carnitine shuttle
Major site of regulation, prevents synthesis and degradation from happening at same time, get it from diet or made from lysine or methionine
33
4 main steps of metabolism part of B oxidation
Dehydration to produce FADH2 Hydration Dehydration to produce NADH Thiolysis (cleaved) to produce acetyl CoA
34
When fasting/starving/diabetes what happens to acetyl CoA
Not enough oxaloacetate to be used in the citric acid cycle so the acetyl CoA is converted into ketone bodies
35
Where does ketogenesis occur and why
In liver and because it depends on the activity of rate limiting enzyme HMG CoA synthase which is found in liver (liver cannot use the ketone bodies but it makes them)
36
Are ketone bodies soluble in blood
Yes. Do not need albumin or lipoprotein
37
What uses ketone bodies for energy
Cardiac and skeletal muscles, kidney, brain cells
38
Excessive ketone bodies can cause
Ketonemia, ketonuria, acidemia
39
Ketone bodies are acidic or alkaline
Acidic
40
Fatty acid synthesis occurs in cytosol in what tissues/ organs
Liver, adipose tissue, lactating mammary gland
41
When does citrate shuttle occur
When citrate concentration in mitochondria is high. It allows acetyl CoA to cross membrane from mitochondrion to cytosol
42
What is the key regulatory enzyme in fatty acid production
Acetyl CoA carboxylase. transfers acetyl coA to TCA
43
What activates and deactivates Acetyl Coenzyme Carboxylase
citrate activates, palmitoyl CoA deactivates. (Short term) Insulin activates, glucagon and epinephrine deactivates (long term)
44
What is malonyl CoA
inhibitor of carnitine shuttle. prevents split up of acyl and coA. Substrate that provides the carbon for the formation of palmitate (product of fatty acid synthesis)