Lipids Flashcards

1
Q

Chylomicrons

A

Transport exogenous lipids from intestines to tissues.

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2
Q

VLDL/IDL/LDL

A

Transport endogenous lipids from liver to tissues.

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3
Q

HDL

A

Transports excess lipids from tissues back to liver.

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4
Q

ApoB100

A

Helps with endocytosis of LDL

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5
Q

ApoCII

A

Activates LPL to free fatty acids from the triglycerides

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6
Q

ApoE

A

Helps the lipoprotein bind to the cell.

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7
Q

Pathway of chylomicrons

A

Intestines –> Lymph –> Blood –> ApoCII frees fatty acids –> Back to liver for disassembly

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8
Q

What tissues have the greatest need for fatty acids?

A

Adipose tissue, muscle tissue, adrenal glands, gonads, lactating mammary glands

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9
Q

Pathway of Lipoproteins

A

VLDL + ApoB100 leave liver –> blood –> ApoCII and ApoE picked up from HDL –> ApoCII activates LPL, FFAS freed –> IDL –> Returns ApoCII and ApoE –> LDL Gives up cholesterol

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10
Q

What happens to LDL particles?

A

They are returned to the liver or scavenged by macrophages

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11
Q

What apolipoprotein is associated with foam cells?

A

LDL (foam cells formed when macrophages take up LDL)

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12
Q

Pathway of HDL

A

HDL + ApoE + ApoCII leave liver –> Gives ApoE and ApoCII to VLDL –> Takes them back from IDL –> Picks up excess cholesterol for delivery to the liver

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13
Q

Where does ketogenesis occur?

A

Liver - mitochondria

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14
Q

Where does cholesterol synthesis occur?

A

Liver - cytosol

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15
Q

What tissues synthesize cholesterol?

A

Brain, ovaries, testes, intestines, liver (BOTIL)

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16
Q

What process is mevalonate associated with?

A

Cholesterol synthesis

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17
Q

How do statins work?

A

They compete with HMG CoA for access to HMG-CoA reductase (short half-life)

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18
Q

What regulates cholesterol synthesis? Where is it located?

A

SREBP in ER

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19
Q

What phenotypes does SREBP impact?

A

HMG-CoA reductase, LDL receptor expression

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20
Q

What hormones can be made from cholesterol?

A

Progesterone, aldosterone, cortisol, estradiol, testosterone (PACET)

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21
Q

In what process does succinyl CoA serve as a source of CoA?

A

Oxidation of ketone bodies

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22
Q

Where do animals get fatty acids from?

A
  • Diet
  • Storage (adipocytes)
  • Converting carbohydrates to fats
  • Autophagy
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23
Q

Where are triglycerides stored?

A

-Adipose tissue
- Between muscle fibers and within muscle cells

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24
Q

What tissues respond to signals from glucagon?

A

Liver & skeletal muscle

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25
Q

What are the three lipases used in triglyceride breakdown?

A
  • Hormone-sensitive lipase (HSL)
  • Adipose Triglyceride Lipase (ATGL)
  • Monoacylglycerol lipase (MGL)
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26
Q

What does albumin bind to?

A

Fatty acid transporters on myocytes

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27
Q

What is the product of fatty acid “activation?”

A

Fatty acyl CoA

28
Q

Where does carnitine come into play?

A

Involved in moving fatty acyl CoA from cytosol to matrix for oxidation

29
Q

What are the products of one round of beta oxidation?

A

1 FADH2, 1 NADH, 1 acetyl CoA

30
Q

What does isomerase do?

A

It converts cis alkenes to trans and can move the alkene into the AB position.

31
Q

What does reductase do?

A

It can reduce two adjacent alkenes into one (in the position between the two original alkenes)

32
Q

What do trans fatty acids do in the body?

A

They activate SREBP, leading to increased cholesterol synthesis.

33
Q

Which fatty acids need isomerase and reductase enzymes?

A

Unsaturated fatty acids

34
Q

Which fatty acids need to be oxidized in the peroxisome?

A

Branched and very long chain fatty acids

35
Q

What is different when FAs are oxidized in the peroxisome?

A

The FADH2 is used to make H2O2, which is broken into H2O and O2 by catalase.
CPT-I and CPT-II aren’t necessary

36
Q

Where does beta oxidation occur?

A

Mitochondrial matrix (liver, brain, adipose tissue, muscle tissue)

37
Q

What process is propionyl CoA associated with?

A

Oxidation of odd-chain fatty acids

38
Q

What differs about how plants carry out beta oxidation?

A

They oxidize almost entirely within peroxisomes

39
Q

Which process needs bicarb, biotin/B7, ATP, and B12?

A

Oxidation of odd-chain fatty acids

40
Q

Which process involves creating succinyl CoA?

A

Oxidation of odd chain fatty acids.

41
Q

What are the conditions for fatty acid synthesis?

A

Excess acetyl CoA and plentiful ATP

42
Q

In plants, where does fatty acid synthesis occur?

43
Q

Where does fatty acid synthesis occur?

A

In the cytosol

44
Q

What are the two sources of citrate used in fatty acid biosynthesis?

A
  • Excess acetyl CoA combining with OAA
  • Reversal of aconitase reaction caused by ATP inhibiting isocitrate dehydrogenase
45
Q

What does the tricarboxylate transport system do?

A

It creates and moves citrate across the IMM and into the cytosol for FA synthesis.

46
Q

What happens to the OAA (from citrate) in the cytosol?

A

Malate –> Pyruvate –> MPC
*Malate to pyruvate generates NADPH

47
Q

What are the 2 sources of NADPH in fatty acid biosynthesis?

A
  • Conversion of malate to pyruvate
  • Pentose phosphate pathway (PPP)
48
Q

Where is the NADPH concentration highest in the cell

A

In the cytosol (where fatty acid synthesis occurs)

49
Q

Where is the NADH concentration highest in the cell?

A

In the mitochondria (beta oxidation generates NADH)

50
Q

What is the “activation” product needed for fatty acid synthesis?

A

Malonyl CoA

51
Q

What process is malonyl CoA associated with?

A

Fatty acid synthesis

52
Q

What molecule inhibits CPT-I?

A

Malonyl CoA

53
Q

What is the regulatory step of fatty acid synthesis?

A

Creation of malonyl CoA via ACC

54
Q

What are the 2 components of ACC?

A

Biotin carboxylase (takes CO2 off of bicarb)
Transcarboxylase (gives CO2 to ACoA)

55
Q

Where is the thiol on the ACP located?

A

Phosphatidic acid prosthetic group

56
Q

What enzymes are used to elongate fatty acids?

A

Elongase and desaturase

57
Q

Where does FA desaturation/elongation occur?

A

ER or mitochondria

58
Q

What process involves electrons being transported from NADPH to Cyt B reductase and Cyt B?

A

Desaturation of fatty acids

59
Q

What is linoleate needed for?

A

To make arachidonic acid

60
Q

What is linolenate needed for?

A

To make omega 3s like DHA and EPA

61
Q

Pathway of arachidonic acid

A

Cleaved off membrane by phospholipase A2
Lipoxygenase converts to leukotrienes
COX converts to PGH2
PGH2 can be converted to thromboxane, prostaglandins, and prostacyclin

62
Q

What pathways are associated with phosphatidic acid?

A

Synthesis of triglycerides and phospholipids

63
Q

What is the “activation” product for synthesis of triglycerides and phospholipids?

A

Phosphatidic acid

64
Q

What molecules are used to elongate fatty acids in the mitochondria?

A

Acetyl CoA (reversal of beta oxidation)

65
Q

What molecules are used to elongate fatty acids in the ER?

A

Palmitate condensed with malonyl CoA