Vitamins and Lipids - Skildum Flashcards

1
Q

After ingestion, how do triacyglycerols travel through the gut lumen?

A

The gall bladder secretes bile salts that emulsify the TG’s.

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2
Q

What is the next step of TG’s after being emulsified by bile salts?

A

Lipase and colipase released from the pancreas breaks TG’s into a fatty acid and 2 monoacyglycerols.
They are then reemulsified in a bile salt micelle.

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3
Q

What happens to the micelle containing 2 Monacyglycerols and a TG?

A

They are taken up by intestinal epithelium and Triacyglycerols are reformed. Then they are packaged in chylomicrons and transported through the lymph to get to the blood.

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4
Q

What is the major apoprotein in chylomicrons?

A

ApoB-48

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5
Q

What is the difference between ApoB-48 in chylomicrons and the ApoB-100 found in hepatocytes?

A

They come from the same gene in DNA. The difference is that after transcription, the RNA that makes ApoB-48 is EDITED. A stop codon is added in producing a smaller mRNA and protein

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6
Q

How does HDL affect chylomicrons after they have entered the blood?

A

HDL transfers ApoCII and ApoE onto the nascent chylomicron transforming it into a mature chylomicron

Thats metamorphosis! (random comment to no one)

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7
Q

What activates Lipoprotein Lipase (LPL) ?

What does it do?

A

LPL is activated by ApoCII.
LPL is found in the capillary beds of muscle and adipose tissue.
LPL cleaves chylomicrons into FA’s, glycerol, and chylomicrons remnants

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8
Q

After LPL breaks up the chylomicron. Where do the FA’s, glycerol, and chylomicron remnants go?

A

FA’s: Oxidized in muscle or stored as TG’s in adipose tissue

Glycerol: Back to the liver

Chylo Remnants: Back to the liver

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9
Q

FA’s and cholesterol grabbed by the liver from chylo-remnants can be repackaged to serve a very similar function as chylomicrons. Explain

A

Can be repackaged with ApoB-100 as VLDL (very low density lipoprotein).

VLDL also delivers FA fuels to the body tissues

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10
Q

Why is it only possible for adipose tissue to store FA’s as TG’s in the fed state?

A

BECAUSE the glycerol-3-phosphate backbone required to form TG’s can only be produced by glycolysis in adipocytes

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11
Q

What kinds of cells serve as a storage reservoir for Vitamin A?

A

Stellate cells of the liver

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12
Q

What proteins are important for blood transport of retinol and retinoic acid?

A

Retinol = RBP (retinol binding protein)

Retinoic Acid = Complexes with albumin

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13
Q

Active form of Vitamin A?

A

All-trans-retinol

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14
Q

Rod cell rhodopsin is a complex of two molecules:
Opsin and _______.
When light strikes it a conformation change then converts _______ to _________.

A

Rod cell rhodopsin is a complex of two molecules:
Opsin and cis-retinal.
When light strikes it, a conformation change then converts cis-retinal to trans-retinal.

This conversion activates a g-protein and Na channel –> boom sight!

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15
Q

How does Vit A affect the immuen system?

A

Retinoic acid actually plays a role in maturing dendritic cells and recruiting antibody-secreting cells to the small intestine.

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16
Q

Complications of Vit A Deficiency?

A
Anorexia
Retarded growth
Infections
Alopecia
Epithelial cell keratinization
Night blindness, xeropthalmia, Bitot's spots (keratin build-ups)
17
Q

Most important complication to remember with Vit A toxicity?

A

Teratogenic effect

18
Q

Vit E deficiency is rare unless you have an absorption problem. Premies, Chrohn’s, short bowel, etc.
What would the clinical manifestations include?

A

Myopathy
Hemolytic anemia
Peripheral neuropathy
Loss of vibratory sense - ataxia

19
Q

Vit E function?

A

Cellular oxidative stress defense
Especially in membranes

Possibly why myopathy occurs without it

20
Q

2 main forms of Vit K. Phylloquinone and Menaquinone. Where are they found?

A

Phylloquinone = leafy green vegetables

Menaquinone = produced by fermentation (in gut, or can be found in cheese)

21
Q

Which vitamin inhibits Vitamin K absorption and metabolism?

A

Vit E

22
Q

How could Vit K deficiency result in a patient with increased prothrombin time and increased bleeding?
(Rare, by the way)

A

Vitamin K acts as a cofactor for gamma-glutamyl carboxylase.
Which activates blood-clotting proteins

Factor 9, 7a, 10, and prothrombin are all Vit-K-Dependent!

23
Q

What foods is Vitamin D found in?

A

Animal origins:

liver, eggs, fish, dairy products, shitake mushrooms

24
Q

In order to synthesize Vit D de novo, what organs are required?

A

Skin, liver, kidney

25
Q

Why is the parathyroid gland important vor Vit D synthesis?

A

In order for kidney to convert Vit D to its active form it must be acted upon by PTH, produced int he Parathyroid gland.

PTH is produced in response to low calcium conentrations

26
Q

When Vit D binds to VDR it induces transcription events to increase Ca in the blood. What are some of these proteins created?

A

Ca channel TRPV6 at the intestinal brush border, calbindin in cytoplasm, Ca-ATPase pumps on basolateral membrane, and claudin to allow more Ca across tight junction.

27
Q

Vit D is the most likely Vitamin to have toxic effects. What are the effects?

A

Calcification of soft tissues (kidneys, heart, lungs, vessels)
Hyperphosphatemia
Hypertension

28
Q

Problems associated with Vit D deficiency?

A

Rickets - seizures, growth retardation, failure of bone mineralization
Osteomalacia is the adults form

29
Q

most calorically dense food?

A

fat!

30
Q

Which molecule’s function is to maintain cholesterol and apoprotein homeostasis.

A

HDL