Phospholipid and Glycolipid Metabolism Flashcards

(34 cards)

1
Q
A
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2
Q

Lipid Nomenclature

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3
Q

Roles of Phospholipids

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4
Q

Glycerophospholipids

A
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5
Q

Glycerol 3 phosphate is produced from which of the following outside of the liver?

Glycerol

Glyceraldehyde 3 Phosphate

Dihydroxyacetone phosphate

Pyruvate

Lactate

A

Dihydroxyacetone phosphate — This is how G3P is made outside the liver.

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6
Q

Phosphatidic Acid

A
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7
Q

Sphingolipids

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8
Q

Types of Sphingolipids

A
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9
Q

Phospholipid Structures

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10
Q

Cerebroside Structures

A
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11
Q

Ganglioside Structure

A
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12
Q

GM1(a ganglioside) Can be best described bt which one of the following terms?

Glycerophospholipid

Cerebroside — only one sugar not two

Phospholipid — there’s no phosphate so its not this.

Diglyceride

Glycolipid

A

Glycolipid — lipid to which sugars are attached. (A better term would be glycosphingolipid)

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13
Q

Phospholipid Metabolism

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14
Q

Phospholipid Structures

Phosphatidylcholine and Phosphatidylethanolamine

A
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15
Q

More Phospholipid Structures:

Phosphatidylserine and phosphatidylinositol

A
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16
Q

Even More Phospholipid Structures:

Phosphatidyl Glycerol and Cardiolipin

17
Q

Structures of Phosphatidic Acid and Sphingomyelin

18
Q

Phospholipid Nomenclature

19
Q

More Phospholipid Nomeclature

20
Q

Simplified View of Phospholipid Synthesis

21
Q

Partial Rationale for Phospholipid Synthesis

22
Q

Which tissue will utilize the glycerol pathway?

Brain

Red Blood Cell

Intestine

Liver

Muscle

A

Liver — only the liver has glycerol kinase so only the liver can use glycerol to get to phospholipid synthesis.

23
Q

What other pathway utilizes a head group activation process?

Glycolysis

Glycogen synthesis

Glycogenolysis

HMP Shunt

Fatty Acid Degradation

A

Glycogen synthesis

24
Q

Individual has a primary carnitine deficiency. Triglyceride synthesis in the liver would be expected to be which one of the following compared to an individual with no carnitine deficiency?

Increased

Decreased

Same

25
Role of Plasmalogens
26
Mitochondrial Function may be compromised by which disorder? Typ 1 Diabetes Type 2 Diabetes Zellwedgers Syndrome Galactosemia Fructokinase Deficiency Pompe Diseases
Zellwedgers Syndrome — lack of peroxisomes.
27
Zellwedgers syndrome would lead to an accumulation of which one of the following? Bicarboxilc acids Branched Chain Fatty Acids Propionyl CoA Carnitine
Branched Chain Fatty Acids
28
Biosynthesis of Sphingosine
29
Vitamin B6 was also required for which one of the following enzymes? Glycogen Synthase Glycogen Phosphorylase Pyruvate dehydrogenase Isocitrate Dehydrogenase Transketolase
Glycogen Synthase — No cofactors required Glycogen Phosphorylase — Requires B6 Pyruvate dehydrogenase — Requires the big 5 Isocitrate Dehydrogenase — requires NAD Transketolase — Requires B1
30
Synthesis of Ceramide
31
Biosynthesis of Sphingomyelin
32
Sphingomyelin Degredation
33
Glycerophospholipid Degredation
34
Ganglioside Function