W1-L2-cellular metabolism 2 lipids Flashcards

1
Q

fatty acids

A

free fatty acid and glycerol
ester linkage
neutralise the -COOH group

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2
Q

Fatty acid metabolism produce what?

A

Acyl CoA

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3
Q

Fat sources

A

diet
de novo biosynthesis (liver)
adipose tissue

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4
Q

bile-production storage and function

A

produced in the liver
stored in the gall bladder
function to emulsify fat, providing larger surface area of lipase action, absorption, digestion of FADEK

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5
Q

bile salt deficiency

A

steatorrhea, most of the fat pass in the small intestine as undigested and unabsorbed

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6
Q

orlistat

A

drugs used to reduced fat absorption
potent inhibitor of lipase gastric and pancreatic
used to treat obesity
side effects abdominal pain, frequent flatus and defecation

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7
Q

lipid transport by

A

lipoprotein

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8
Q

lipoprotein types

A

subdivided as chylomicrons, VLDL, LDL, IDL, HDL

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9
Q

chylomicrons

A

dietary fat transport, arise from small intestine

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10
Q

low density lipoprotein

A

cholesterol transport, arise from IDL

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11
Q

very low density lipoprotein

A

arise from liver, endogenous fat transport

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12
Q

intermediate density lipoprotein

A

arise from VLDL, precursor of LDL

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13
Q

high density lipoprotein

A

arise from the liver, reverse cholesterol transport

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14
Q

chylomicrons pathway transport

A

into the blood stream
acquire apoproteins form HDL
binding of apoproteins to lipoprotein lipase at skeletal muscle, adipose tissues and heart
breakdown into FA and glycerol
FA goes to muscles adipose tissue
acquire apoprotein from HDL again and goes to liver

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15
Q

where CM enter the bloodstream

A

left subclavian vein

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16
Q

lipoprotein lipase function and location

A

heart, skeletal muscles and adipose tissue

17
Q

lipoprotein life cycle

A

VLDL-breakdown to release FA and glycerol to muscle and adipose tissue to become a lipid remanent, gives apoprotein to HDL to become a IDL
IDL-receive cholesterol esters from HDL to become LDL
transport cholesterol to tissues or get cleared by macrophage and transported back to liver

18
Q

Fatty acid to Acyl CoA species

A

B- oxidation, breakdown of 2 high energy bond from ATP to AMP

19
Q

where does Acyl CoA species generated

A

outer mitochondrial membrane

20
Q

Acyl CoA transport

A

carnitine shuttle- coupling of Acyl CoA to carnitine to form Acyl carnitine, transported to matrix by translocase

21
Q

primary carnitine deficiency

A

B-oxidation cannot proceed as Acyl CoA cannot be transported into matrix
encephalophaties results

22
Q

B-oxidation

A

oxidation hydration and thiolysis sequence to convert acyl CoA to acetyl CoA species

23
Q

10 B-oxidation produce how many acetyl CoA

A

11

24
Q

ketone body formation

A

formed by B-oxidation when the fatty acid metabolism >carb metabolism as oxaloacetate is needed

25
Q

fatty acid biosynthesis

A

involves 2 enzymes: acetyl CoA carboxylase and fatty acid synthase
condensed molecules: acetyl CoA and malonyl CoA
enzyme involved KR, DH, ER
growing fatty acyl attached to acyl carrier protein

26
Q

difference between synthesis and degradation

A

ACP vs CoA carrier
NADPH vs NAD+ and FADH reducing power
cytoplasm vs matrix location

27
Q

de novo FA biosynthesis location

A

liver, adipose tissue and lactating breast

cancer relationship as cancer cells use fatty acid metabolism as energy source

28
Q

enzyme catalysing initial step of B-oxidation

A

Acyl CoA dehydrogenase family broken down to

small, medium, long and very long CACAD

29
Q

MCADD

A

autosomal recessive

unable to go without food for more than 12h , no metabolism fat dependent

30
Q

cholesterol esters formation

A

cholesterol+leucin in presence of LCAT

31
Q

anatomy of a lipoprotein

A

single layer of phospholipids with cholesterol esters core and proteins presents