Lipid Transport Flashcards

(43 cards)

1
Q

Lipids are soluble in _________ solvents

A

Non-Polar

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2
Q

Function of lipids

A

Source of energy
Signaling
Plasma membrane structure

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3
Q

How do Dietary Lipids get to Body cells

A

Via Lipoproteins

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4
Q

Where does chylomicron is produced?

A

Intestine (small intestine)

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5
Q

What is a chylomicron

A

Molecule composed of Lipid + Lipoprotein

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6
Q

Chylomicron express which surface protein

A

Apo B84

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7
Q

Where do Chylomicrons go after formation?

A

Lympathic channels

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8
Q

What happens once a Chylomicron runs out of fatty acids

A

It is processed by the Liver into cholesterol

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9
Q

Where do VLDL is produced?

A

Liver

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10
Q

Which surface protein is representative of VLDL?

A

Apo B100

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11
Q

What is the function of VLDL?

A

Same as Chylomicron

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12
Q

What happens once VLDL has run out of fatty acids

A

It becomes IDL

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13
Q

What routes do IDL have?

A
  1. Processed by liver
  2. Formation of LDL (High in cholesterol) and then absorbed by peripheral cells
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14
Q

LDL receptor interact with which molecule?

A

Apo B100

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15
Q

What are HDL function?

A

Donates ApoC2 and ApoE to chylomicron and VLDL

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16
Q

What is ApoC2 function?

A
  • Activation of Lipoprotein Lipase = Breakdown of TG into FA
  • Let FA enter into pheripheral cells
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17
Q

What is ApoE function?

A

Allows reuptake of remmant lipoproteins for recycling in the Liver

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18
Q

How does an inmature HDL becomes a Mature HDL?

A

Via LCAT enzyme (Activated by Lipoprotein A1)

19
Q

Apo B48 function

A

Transport of Chylomicrons into lymphatics

20
Q

Apo B100 function

A

Binds to LDL for uptake of LDL by peripheral cells (ENDOCITOSIS)

21
Q

Abetalipoproteinemia inheritance pattern

A

Autosomal Recesive

22
Q

Which surface protein is deficient in Abetalipoproteinemia?

A

ApoB48 / ApoB100

23
Q

Abetalipoproteinemia is characterized by absence of which Lipoproteins?

A

Chylomicron
VLDL
LDL

24
Q

Clinical features of Abetalipoproteinemia?

A

Severe fat malabsorption + FTT + Deficiency of fat-soluble vitamins

25
Treatment of Abetalipoproteinemia?
Vitamin E
26
Familial Hypercholesterolemia inheritance pattern
Autosomal Recessive
27
Which surface protein is deficient in Familial Hypercholesterolemia
LDL Receptor or Apo B100
28
Which Lipoproteins are increased in Familial Hypercholesterolemia
LDL (++) Cholesterol
29
Familial Hypercholeterolemia is associated to
Early-onset Atherosclerosis (Accelerated)
30
Familial Hypercholeterolemia is associated to
Early-onset Atherosclerosis (Accelerated)
31
Familial Dyslipidemias follows which kind of inheritance pattern
Autosomal Recessive
32
Dysbetalipoproteinemia is caused by deficient
ApoE
33
Which lipoproteins are affected in Dysbetalipoproteinemia
Increased Chylomicrons and VLDL
34
Dysbetalipoproteinemia clinical features
Accelerated Atherosclerosis + Xanthomas
35
Familial Hypertriglyciridemia is caused by
Excessive production of VLDL
36
Familial Hypertriglyciridemia is associated to
Pancreatitis
37
Hyperchylomicronemia is caused by deficient
Lipoprotein Lipase or ApoC2
38
Hyperchylomicronemia is consistent with elevation of __________
39
Hyperchylomicronemia is consistent with elevation of __________
Chylomicrons / Triglycerides / Cholesterol
40
Hyperchylomicronemia clinical features
Pancreatitis + Xanthomas + Hepatosplenomegaly
41
Hyperchylomicronemia main feature for diagnosis
Creamy layer of fat in supernatant
42
Association between Hyperchylomicronemia and Atherosclerosis
NON-EXISTENT
43
Association between Hyperchylomicronemia and Atherosclerosis
NON-EXISTENT