Chapter 17- Lipid II Phospholipids, Glycosphingolipids, And Cholesterol Flashcards

1
Q

What lipids have an essential role in the synthesis of plasma lipoproteins?

A

phospholipids and glycosphingolipids

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2
Q

what lipids function in transduction of messages from cell surface receptors to secondary messengers that control cellular processes?

A

phospholipids and glycosphingolipids

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3
Q

What lipids function as surfactant?

A

Phosphatidylcholine

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4
Q

Cholesterol is the precursor of what?

A

bile acids, steroid hormones, 7-dehydrocholesterol

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5
Q

A ceramide is composed of?

A

LCFA attached to amino group of sphingosine

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6
Q

a sphingomyelin is composed of?

A

ceramide and phosphorylcholine

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7
Q

Synthesis of phosphatidylcholine requires what nuclei acid?

A

cytidine triphosphate

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8
Q

accumulated sphingomyelin characterized as?

A

Niemann-Pick disease

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9
Q

cerebrosides formed from?

A

ceramide and UDP-sugars

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10
Q

accumulation of cerebrosides characterized as?

A

Gaucher’s, Krabbe’s disease

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11
Q

Sulfatides formed from?

A

addition of sulfate group to cerebrosides

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12
Q

accumulation of sulfides characterized as?

A

metachromatic leukodystrophy

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13
Q

Gangliosides formed from?

A

cerebrosides by addition of sugars

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14
Q

accumulation gangliosides characterized as?

A

GM1 gangliosidosis, Tay-Sachs disease

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15
Q

What toxin inhibits sphingolipid synthesis?

A

fumonisin

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16
Q

What is an important constituent of the myelin sheath of nerve fibers?

A

sphingomyelin

17
Q

Enzyme deficient in Tacy-Sachs disease?

A

Hexosaminidase A

18
Q

Enzyme deficient in Fabry’s disease?

A

alpha-galactosidase

19
Q

Enzyme deficient in Metachromatic leukodystrophy?

A

arylsulfatase A

20
Q

Enzyme deficient in Krabbe’s disease?

A

beta-galactosidase

21
Q

Enzyme deficient in Gauchers disease?

A

beta-glucosidase

22
Q

Enzyme deficient in Niemann-Pick disease?

A

sphingomyelinase

23
Q

Enzyme deficient in Farber’s disease?

A

ceramidase

24
Q

What tissues have the largest contribution of cholesterol synthesis?

A

liver, intestine, adrenal cortex, reproductive tissues

25
Q

biosynthesis of mevalonate occurs where?

A

cytosol

26
Q

Where are carbons that form cholesterol derived from?

A

all C’s from acetate

27
Q

What molecule provides reducing equivalents for cholesterol synthesis?

A

NADPH

28
Q

Reactions from mevalonic acid to cholesterol contain how many carbons at each reaction?

A

mevalonic acid: 6C’s -> 6C’s -> 5C’s -> 5C’s -> 10C’s -> 15C’s -> 30C’s -> 30C’s -> cholesterol: 27C’s

29
Q

If bile acids are increased this is indicative of what disease?

A

hepatocellular disease or obstructive jaundice

30
Q

Bile salt that is toxic, can cause hemolysis & fever

A

Lithocholic acid

31
Q

Symptoms of hyperbile acidemia

A

pruritus, steatorrhea, hemolytic anemia, further injury liver injury

32
Q

What is cholelithiasis?

A

gallstones, precipitation of cholesterol in bile

33
Q

What is lithogenic?

A

(stone forming) mole ratio of bile salts & PLs to cholesterol is less than 10:1

34
Q

What is used to convert phosphatidylethanolamine to phosphatidylcholine?

A

3SAM -> 3SAH

35
Q

glycerol 3-phosphate to phosphatidic acid?

A

2 fatty acyl-CoA -> 2 CoA-SH