TG, PL, SPL Flashcards

1
Q

TG and PL are synthesized _

A

cytosolic side of ER and lesser extent OMM

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2
Q

Common intermediate of TG and PL synthesis

A

Phosphatidic Acid

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3
Q

Major stored form of E in adipose

A

TG

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4
Q

Formation of TG

A

Glyercol 3P > PA > diacyl glycerol > TG

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5
Q

CM transports TG to _ and dietary cholesterol to _

A

Various tissues(muscle adipocytes)
Liver only

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6
Q

Apoproteins on CM

A
  • ApoC…activates lipoprotein lipase > hydrolyze TG > release F.A. for storage/E in adipocytes or muscle
  • ApoB48…marker of CM
  • ApoE…recognition protein
  • ApoB48, ApoE responsible for cholesterol transport to liver by remnant CM via endocytosis
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7
Q

LDL has which apoprotein?
Deficiency can cause?

A
  • Apo100
  • Hypercholesterolemia
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8
Q

Formation of PL(de novo)

A

PA > CDP-DAG by cytidyl transferase…+ serine > PS and CMP
or CDP-DAG + inositol > PI(CNS)

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9
Q

Dipalmitoyl PC deficiency in lung

A

Respiratory distress syndrome

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10
Q

_ cause skin cancer by activating PKC
They are structural analogues of _

A
  • Phorbol esters
  • DAG
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11
Q

PL salvage pathway

A

Methionine intake limited > choline re-salvaged > choline phosphate > CDP-choline via cytidyl transferase…+ DAG > PC

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12
Q

Defect in salvage pathway leads to(kinase or transferase)

A

Fatty liver
(DAG accumulates > TG)

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13
Q

PL drug carrier _

A

Liposome

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14
Q

Hydrolyze…
PLA1:
PLA2:
PLC:
PLD:

A
  • first ester bond
  • fatty acyl ester bond at position 2
  • releases head groups of PL + DAG
  • releases head groups + PA
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15
Q

T/F: Sphingolipids are involved in ABO blood types

A

True

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16
Q

Synthesis of SPL occurs in _

A

ER membrane

17
Q

RDS in SPL synthesis

A

Serine palmitoyl transferase(B6)
Palmitic acid + serine

18
Q

SPL synthesis steps

A

after RDS rxn…keto > sphinganine > dihydroceramide > ceramide via cermide synthase

19
Q

PAPS?

A
  • Phosphoadenosyl phosphosulfate
  • Sulfates neutral glycolipids > sulfatids
20
Q

SPL catabolism(lysosomal enzymes)

A

Release CBHY > Ceramide > sphingosine + F.A. via ceramidase(amide)

21
Q

Sphingolipidoses characterized by (4)

A
  • abnormal amount of SPL > organomegaly
  • Defect in catabolic enzymes only
  • Affect all tissues the same
  • Mental retardation
22
Q

Gaucher’s:
Krabbe’s:
Nielmann-pick:
Tay Sacch’s:
Farber’s:

A
  • Glucocerebrosidase deficiency
  • Galactocerebrosidase deficiency
  • Sphingomyelinase deficiency
  • Hexoaminidase deficiency
  • Ceramidase deficiency
23
Q

Opposed to sphingolipidoses, demyelination/degradation causes _

A

Multiple sclerosis