Basic structure of lipids and lipoprotein

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Last updated 4:49 PM on 7/22/26
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168 Terms

1
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Lipids are soluble in what type of solvents?

Non‑polar organic solvents such as benzene, chloroform, ether, hot alcohol, acetone

2
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What is the difference between fat and oil at room temperature?

Fat is solid, oil is liquid

3
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What elements mostly compose lipids?

Carbon, hydrogen, oxygen

4
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What are the four main classes of lipids?

Simple lipids, compound lipids, derived lipids, lipids complexed to other compounds

5
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Give examples of simple lipids.

Triacylglycerols (TAGs), waxes

6
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Give examples of compound lipids.

Phospholipids, non‑phosphorylated lipids

7
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Give examples of derived lipids.

Fatty acids, steroids, prostaglandins, cholesterol

8
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Give examples of lipids complexed to other compounds.

Proteolipids, lipoproteins

9
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What is the main storage form of energy in lipids?

Triacylglycerols

10
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Which lipids are structural components of biomembranes?

Phospholipids, glycolipids, cholesterol

11
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Which lipids act as metabolic regulators?

Steroid hormones and prostaglandins

12
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Which lipids act as surfactants and emulsifying agents?

Amphipathic lipids

13
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What lipid function provides electrical insulation?

Lipids in neurons

14
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What lipid function provides thermal insulation?

Subcutaneous fat

15
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What lipid function cushions internal organs?

Pads of fat

16
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Which vitamins require lipids for absorption?

Fat‑soluble vitamins A, D, E, K

17
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What is the general formula of saturated fatty acids?

CH3‑(CH2)n‑COOH

18
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Give examples of saturated fatty acids.

Acetic acid, butyric acid, palmitic acid, stearic acid

19
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Where are palmitic and stearic acids found?

Body fat

20
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What defines unsaturated fatty acids?

Presence of one or more double bonds

21
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What configuration do naturally occurring unsaturated fatty acids have?

Cis configuration

22
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What configuration of fatty acids is formed during metabolism?

Trans fatty acids

23
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What are essential fatty acids?

Linoleic acid (ω6) and linolenic acid (ω3)

24
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Can arachidonic acid be synthesized in the body?

Yes, if essential fatty acids are supplied in the diet

25
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What is the nutritional importance of penta‑enoic acid in fish oils?

It is an ω3 unsaturated fatty acid

26
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What are eicosanoids derived from?

20‑carbon arachidonic acid

27
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Name the families of unsaturated fatty acids.

ω3 (linolenic), ω6 (linoleic, arachidonic), ω9 (oleic)

28
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Where are trans fatty acids commonly found?

Dairy products, hydrogenated oils, fast food, processed foods, bakery products

29
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What are the adverse effects of trans fatty acids?

Altered blood lipids, systemic inflammation, endothelial dysfunction, insulin resistance, obesity

30
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What is an acylglycerol?

Ester of fatty acids with glycerol

31
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What are the classes of acylglycerols?

Monoacylglycerols, diacylglycerols, triacylglycerols

32
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What is the difference between simple and mixed TAGs?

Simple TAGs have identical FAs, mixed TAGs have different FAs

33
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Where is PUFA commonly esterified in TAGs?

At the β‑carbon of glycerol

34
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What is the energy yield of fatty acids compared to carbs/proteins?

9 kcal/g vs 4 kcal/g

35
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Where are TAGs synthesized mainly?

Liver

36
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How are TAGs transported in blood?

As lipoproteins

37
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Where are TAGs stored?

Adipose tissue

38
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What is the simplest phospholipid?

Phosphatidic acid

39
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What is the amphipathic nature of phospholipids?

They have hydrophobic tails and hydrophilic heads

40
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What is the main constituent of cell membranes?

Glycerophospholipids

41
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What is the main constituent of myelin sheath?

Sphingophospholipids

42
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What is the role of phospholipids in lipoproteins?

Transport of TAGs and cholesterol

43
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What is the steroid nucleus of cholesterol called?

Cyclopentanoperhydrophenanthrene nucleus

44
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What are the structural features of cholesterol?

Four fused rings, hydroxyl at C‑3, double bond at C‑5/C‑6, methyls at C‑10/C‑13, side chain at C‑17

45
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What is the molecular formula of cholesterol?

C27H46O

46
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What is the most important sterol in the human body?

Cholesterol

47
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List functions of cholesterol.

Membrane fluidity, nerve conduction, precursor of bile acids, steroid hormones, vitamin D3

48
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Where does fatty acid biosynthesis occur?

Cytoplasm of liver, lactating mammary gland, adipose tissue

49
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What are the precursors for fatty acid biosynthesis?

Excess dietary carbohydrates and proteins

50
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How are unesterified fatty acids transported in blood?

Bound to albumin

51
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What provides 2‑carbon units in fatty acid biosynthesis?

Malonyl‑CoA

52
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What is the end product of fatty acid synthase complex?

Palmitic acid

53
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What are the major sources of NADPH for lipogenesis?

Pentose phosphate pathway, cytosolic NADP+‑dependent malic enzyme

54
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Where does β‑oxidation occur?

Mitochondria

55
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Where are fatty acids activated before β‑oxidation?

Cytoplasm

56
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What transports fatty acyl‑CoA into mitochondria?

Carnitine carrier system

57
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What is released in each cycle of β‑oxidation?

Acetyl‑CoA, NADH, FADH2

58
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How many cycles of β‑oxidation does palmitic acid require?

7 cycles

59
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What is the final product of odd‑chain fatty acid oxidation?

Propionyl‑CoA

60
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What can propionyl‑CoA be converted into?

Glucose (gluconeogenesis)

61
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How does β‑oxidation differ for unsaturated fatty acids?

Depends on whether double bond is at even or odd carbon position

62
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What are ketone bodies?

Water‑soluble compounds formed from acetyl‑CoA in liver and kidney

63
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When are ketone bodies synthesized?

During fasting, starvation, or high‑fat diet

64
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Name functional ketone bodies.

Acetoacetate, β‑hydroxybutyrate

65
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Name the non‑functional ketone body.

Acetone

66
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What is the rate‑limiting enzyme in ketogenesis?

HMG‑CoA synthase

67
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What ketone body is excreted in expired air?

Acetone

68
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What is the order of lipoproteins from most dense to least dense?

HDL > LDL > VLDL > Chylomicrons

69
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What do chylomicrons transport?

Dietary TAGs

70
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What does VLDL transport?

Endogenous TAGs from liver

71
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What does LDL transport?

Cholesterol to tissues

72
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What does HDL transport?

Cholesterol back to liver (reverse transport)

73
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What enzyme degrades TAGs in chylomicrons?

Lipoprotein lipase

74
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What happens to chylomicron remnants?

Taken up by liver

75
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What is VLDL converted into after TAG delivery?

LDL

76
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How is LDL taken up by tissues?

Receptor‑mediated endocytosis

77
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What is the role of HDL in cholesterol metabolism?

Reverse cholesterol transport to liver

78
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What is Type I hyperchylomicronemia caused by?

Lipoprotein lipase deficiency or ApoC‑II defect

79
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What are the clinical features of Type I hyperchylomicronemia?

Pancreatitis, hepatosplenomegaly, eruptive xanthomas, no increased atherosclerosis risk

80
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What is Type IIa familial hypercholesterolemia caused by?

Absent or defective LDL receptors

81
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What are the clinical features of Type IIa familial hypercholesterolemia?

Accelerated atherosclerosis, MI before age 20, tendon xanthomas, corneal arcus

82
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What is Type IV hypertriglyceridemia caused by?

Hepatic overproduction of VLDL

83
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What is the clinical feature of Type IV hypertriglyceridemia?

Pancreatitis

84
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What is Tangier disease caused by?

ABCA1 deficiency

85
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What is the hallmark of Tangier disease?

Severe reduction in HDL

86
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Which lipoprotein particle transports dietary lipids through blood?

Chylomicrons

87
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What lipids are found in the core of chylomicrons?

TAGs and cholesterol esters

88
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What surface protein is characteristic of chylomicrons?

ApoC‑II

89
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What is the energy yield of fatty acids compared to proteins and carbohydrates?

9 kcal/g vs 4 kcal/g

90
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What is the main site of ketone body synthesis?

Liver mitochondria

91
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Which ketone body undergoes spontaneous decarboxylation to acetone?

Acetoacetate

92
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Which lipoprotein is associated with tendon xanthomas?

LDL (Type IIa familial hypercholesterolemia)

93
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Which familial dyslipidemia does not increase risk of atherosclerosis?

Type I hyperchylomicronemia

94
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Which familial dyslipidemia may cause MI before age 20?

Type IIa familial hypercholesterolemia

95
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Which familial dyslipidemia is autosomal recessive with LPL deficiency?
Type I Hyperchylomicronemia
96
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Which familial dyslipidemia is autosomal dominant with defective LDL receptors?
Type IIa Familial Hypercholesterolemia
97
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Which familial dyslipidemia is autosomal dominant with hepatic VLDL overproduction?
Type IV Hypertriglyceridemia
98
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Which familial dyslipidemia is autosomal recessive with ABCA1 deficiency?
Tangier disease
99
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Which familial dyslipidemia causes accelerated atherosclerosis and MI before age 20?
Type IIa Familial Hypercholesterolemia
100
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Which familial dyslipidemia causes pancreatitis without increased atherosclerosis risk?
Type I Hyperchylomicronemia