Lipid Structure Flashcards

1
Q

lipids

A

insoluble in water but soluble in nonpolar organic solvents

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2
Q

simple lipids

A

fats and waxes

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3
Q

fats

A

esters of fatty acids with glycerol (oils are liquid fats)

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4
Q

waxes

A

esters of fatty acids with alcohols

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5
Q

complex lipids

A

phospholipids, glycolipids, lipoproteins

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6
Q

phospholipids

A

glycerophospholipids and sphingophospholipids

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7
Q

glycolipids

A

glycosphingolipids

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8
Q

precursor and derived lipids

A

fatty acids, steroids, bile acids, ketone bodies

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9
Q

fat-soluble vitamins

A

A, D, E, K

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10
Q

lipid function

A

fuel for energy and storage, membrane structure, detergents, signaling molecules, vitamins

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11
Q

energy/storage lipids

A

fatty acids and triglycerides

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12
Q

membrane lipids

A

glycerophospholipids, sphingolipids, cholesterol

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13
Q

detergents

A

bile acids

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14
Q

signaling molecules

A

steroid hormones and prostoglandins

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15
Q

fatty acids structure

A

unbranched, nonaromatic, carboxylic acids (amphipathic)

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16
Q

saturated fatty acids

A

no double bonds

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17
Q

mono-unsaturated fatty acid

A

1 double bond; position of double bond from carbonyl end

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18
Q

polyunsaturated fatty acids

A

classified according to first double bond starting at the last carbon (omega-3)

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19
Q

amphipathic

A

hydrophilic and hydrophobic

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20
Q

solubility of fatty acids

A

short chains (<8 C’s) are soluble in water

21
Q

melting temp of fatty acids

A

melting temp increases with chain length but decreases with double bonds

22
Q

triglyceride

A

glycerol + 3 fatty acid tails; major lipid for energy storage

23
Q
A

glycerophospholipids

24
Q
A

sphingolipids

25
glycolipid
26
glycerophospholipid structure
saturated FA at C-1 and unsaturated at C-2
27
3 major classes of sphingolipids
sphingomyelins, gangliosides, and glycosphingolipids
28
spingomyelin
covers axons in nerves
29
glycosphingolipids
important in brain cerebrosides (head group=glucose or galactose)
30
gangliosides
head group=oligosaccharides; cell-cell signaling
31
sphingolipidoses
lysosomal storage disease --> patients with defective enzymes accumulate sphingolipid intermediates
32
sphingolipidosis diseases
Tay-Sachs, Niemann-Pick, Gaucher's, Fabry's
33
Tay-Sach's
mental retardation, red dots in eyes, blindness, death by 3
34
Gaucher's disease
liver and spleen enlargement, erosion of long bones, mental retardation (most common)
35
Gaucher's onset
mutation in glucocerebrosidase; can develop throughout life depending on enzyme function
36
cholesterol
decreases fluidity at high temps and increases at low temps
37
spur anemia
erythrocyte membranes contain unusual spurs (occurs with severe liver disease)
38
how does spur anemia develop?
increased cholesterol will leak out of liver --> makes way to bone marrow --> gets in erythrocytes and causes spur shape
39
bile acids
made in liver but secreted to gallbladder; amphipathic; emulsifying agents
40
hypercholesterolemia treatment (high cholesterol)
prevention of bile salt uptake by intestinal epithelium
41
cholesterol signaling molecules
steroid hormones
42
fatty acid signaling molecules
prostoglandins
43
prostoglandins
can help with pain and inflammation
44
prostoglandins
can help with pain and inflammation
45
vitamin A
vision, reproduction, bone growth, and epithelial differentiation
46
vitamin D
regulates plasma calcium levels, roles in diabetes, immune system, cardiovascular health
47
vitamin E
anti-oxidant
48
vitamin K
co-enzyme in post-translational modification of blood clotting factors
49
exacerbation of vitamin deficiencies
excessive intake of oils, bile duct obstruction, inflammatory bowel diseases