Dietary Lipids Flashcards

1
Q

Hormonal control of digestion

A

Intake meal - mucosa of jej and duod produce CCK - CCK causes gall bladder to expel bile and panc enzyme - slows gastric contractions - secretion from mucosa responds to low pH chyme and induces panc bicarb to neut - optimal pH. Process increases insulin

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2
Q

Lipases

A

Enzyme of lipid digestion. first in stomach = acid stable lingual lipase. Primary target = short and medium chain FA TAGs (milk)

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3
Q

Emulsification of lipids

A
with aid of bile salts in duod, increase micelle SA
Bile salts (glyco and taurocholate) create stable particles; enzymes adhere to micelles and graze 1 FA at a time
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4
Q

Degrade of TAGs

A

Too large for mucosal uptake

Pancreatic lipase cleaves ester bonds at each end to create 2 FFAs and monoglycerol

Colipase holds panc lipase at interface between lipid and aqueous media and allows exposure of lipase to active site. Activate by chymotrypsin (zymogen). Inhib via Orlistat

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5
Q

Panc neut pH lipid hydrolases in intestine

A

Cholesterol Esterase - removes ester

PLA2 - after PL’s action at C2, remaining Fatty Acyl removed via lysophospholipase leaving soluble glycerophosphate

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6
Q

Lipids enter at brush border

A

Short and Med chain enter without Micelle aid, abs mostly as monoglycerides and FFAs, reassembled into TAG in mucosa. TAG, chol, PL to CM. CM exit mucosa and enter lymph to circulation via thoracic duct

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7
Q

Fate of LCFA and chol in mucosa

A

Upon absorb - LCFA and chol are esterfied. First act to FA-CoA by FA-CoA synthase (thiokinase) with 2 ATP

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8
Q

Fate of SC and MC FA

A

not esterfied: enter portal circulation directly with albumin to liver

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9
Q

mucosal cells and CM

A

Assemble and secrete CM with ApoB100

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10
Q

CMs

A

Sole LP carrier of dietary lipid
In liver - gene transC into ApoB100
In intestine - same gene ApoB100 to ApoB48; mod via transC processing

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11
Q

CM assembly

A

ApoB48 with lipid requires MTP (ER) = microsomal Triglyceride transfer protein

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12
Q

CM role

A

Accelerates transport of TAG, chol esters, and PLs across organelle membrane. As ApoB48 made - lipid begins to associate with it in a process catalyzed by MTP

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13
Q

MTP def

A

Beta lipoproteinemia - deficient assembly of all ApoB bearing lipoproteins (CM, VLDL, IDL, LDL)

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14
Q

CMs function

A

Exocytosed into lacteals of gut. Roles = Seperate fats from water and signal cells, cargo of lipid

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15
Q

HDL and CM

A

Key apoproteins are acquired from HDL that function as roving resevoir of ApoProteins
ApoC 2 - activates LPL
ApoE: hepatic endocytosis of CM

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16
Q

CM empty

A

emptied by membrane LPL and glycerol to liver. LPL held by GPI with Hep Sulfate (SO4 bound). Fat does not go to Liver and Brain via CM

17
Q

LPL variants

A

Cardiac and Skl M 1/15th of rest to indicate constant need

18
Q

Defects in lipid absorb

A

Leads to steatorrhea, def in FAs and fat soluble vits (ADEK) leading to blood clot disorders and dermatitis and others