lipids 1 Flashcards

1
Q

In what three places do lipids exist?

A
  • cell membranes
  • as lipid droplets in adipose tissue
  • in blood lipoproteins
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2
Q

Name the 6 biological functions of lipids

A
  • stored form of energy
  • structural element of membranes
  • enzyme cofactors
  • hormones
  • vitamins A, D, E, K
  • signalling molecules
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3
Q

What are the classes of lipids?

A
fatty acids
triacylglycerol
phospholipid
glycolipid
steroids
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4
Q

What does ‘18:1’ mean in terms of fatty acid nomenclature?

A

18 carbons and 1 double bond

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5
Q

what are linoleic and linolenic acids examples of?

A

essential fatty acids in humans

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6
Q

Why must some fatty acids be consumed in the diet?

A

humans cannot introduce double bonds beyond carbon 9

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7
Q

what 2 benefits does Omega-3 fatty acid have?

A

1 - lowers plasma cholesterol and prevents atherosclerosis

2- lowers triacylglycerol and prevents obesity

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8
Q

what are triacylglycerols esters of?

A

fatty acids and glycerol

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9
Q

what is phospholipid composed of?

A

glycerol bonded to two fatty acids and a phosphate group

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10
Q

what is the main dietary lipid?

A

triacylglycerol

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11
Q

what is the main site of digestion?

A

small intestine

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12
Q

what role do bile salts play in lipid digestion?

A

act as biological detergents to form emulsions and mixed micelles

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13
Q

what enzyme degrades TAG to monoacylglycerol and two fatty acids in the small intestine?

A

pancreatic lipase

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14
Q

What is the second product of digestion of cholesterol esters as well as free fatty acid?

A

cholesterol

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15
Q

What do phospholipids hydrolyse to?

A

fatty acid and lysophospholipid

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16
Q

what do products of lipid digestion form with bile salts in order to be absorbed?

A

mixed micelles

17
Q

what is Steatorrhea?

A

excess fat in faeces

18
Q

which three defects could lead to lipids not being absorbed by cells and potentially steatorrhea?

A

defects in:

  • bile secretion (for secreting bile salts to form mixed micelles and emulsify the fat)
  • pancreatic function (for breaking down molecule)
  • intestinal cell uptake
19
Q

The intestinal cells resynthesize TAG, PL and CE for export but they are insoluble. How is this problem overcome?

A

The are packaged with apoB-48 into chylomicrons

20
Q

How are chylomicrons released from intestinal cells and where to?

A

by exocytosis

into lymph then blood

21
Q

which enzyme hydrolyses TAG in chylomicrons to FA and glycerol?

A

lipoprotein lipase

22
Q

what are chylomicrons depleted of TAG called and where do they go?

A

chylomicron remnants

go to liver

23
Q

what two things can happen to fatty acids (those made when TAG is broken down by lipoprotein lipase)

A
  • oxidised as fuel

- re-esterified for storage

24
Q

in what form is TAG stored in adipose cells?

A

as droplets

25
Q

what releases fatty acid from stored TAG?

A

hormone sensitive lipase (HSL)

26
Q

hormone sensitive lipase is activated by phosphorylation and inactivated by dephosphorylatiom. What activates and deactivates HSL?

A

activates - epinephrine

deactivates - high plasma glucose and insulin

27
Q

which protein forms a complex with fatty acids to transport them through the blood?

A

albumin

28
Q

how are esterified fatty acids carried through the blood?

A

by lipoproteins

29
Q

name the four lipoproteins in order starting with least dense

A

chylomicrons
VLDL
LDL
HDL

30
Q

what can too much LDL lead to?

A

atherosclerosis