Fat oral topics Flashcards

1
Q

how are lipids soulbilized and digested

A

solubilized in bile salts, then degraded by pancreatic lipase in intestines

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2
Q

what does pancreatic lipase generate

A

free FA and mix of mono/diacylglycerides - triacylglycerides are split at 1, 3 positions making 1,2-diacylglycerol and 2 acylglycerol

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3
Q

phospholipid degr

A

at 2 position by pancreatic phospholipase

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4
Q

absorption of fats

A

the products of pancreatic lipase are absorbed into intestinal mucosa cell and re-synthesized into triacyl glycerol

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5
Q

how are triacylglycerols solubilized and transported

A
  • packed into VLDL’s to be released into blood directly - packed into chylomicrons, to be transported in the lymph to reach the blood at thoracic inlet (storage or prod of energy by ox)
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6
Q

uptake of fat

A

VLDLs and chylomicrons are hydrolized to FFA and glycerol in caps of adipose tissue and skeletal muscle using lipoprotein lipase - FFA is absorbed by cell - glycerol into caps to liver to be converted to diOHacetonphosphate -> GNG/GL

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7
Q

name the general steps of beta-ox of even FA

A
  1. dehydration (FADH2 prod) 2. hydration 3. dehydration (NADHH prod) 4. thiolase cleavage
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8
Q

how many cycles of beta ox of even (saturated) FA, and how many Ac~CoA are made

A
  • *n/2-1**
    e. g. 16C/2 - 1 = 7 cycles

N/2= no. of AcCoA

e.g. 16C/2= 8 AcCoA

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9
Q

energy balance of B-ox of (even) FA palmitoyl-CoA

A

8 AcCoA ⇒ 8*12 ATP

7 FADH2 ⇒ 7*2 ATP

7 NADH+H⁺ ⇒ 7*3 ATP

= 131ATP - 2 used in the synth, 129

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10
Q

where does beta-ox of even FA not occur, and why

A

RBC: no mitochondrion

brain: to big to pass blood-brain barrier)

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11
Q

unsaturated: cis vs. trans in B-ox

A

even: trans, uneven: cis (creates bend)

  • uneven beta ox needs 2 extra ATP to convert cis to trans, so that the A,B-enoyl-CoA hydratase of B-ox to function - needs A,B configuration
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12
Q

difference in odd vs. even FA in beta oxidation

A

odd generates 7 fewer ATP’s per cycle:

  • carboxylation of prop-CoA needs 1 ATP
  • succinyl-CoA enters TCA instead of AcCoA -> -6ATP
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13
Q

important co-factors in the reactions of prop-CoA→→→succinyl-CoA

A

biotin

vit. B12; DA-cobalamine

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14
Q

ACP - acyl carrier protein: use in FA synthesis

A

“carries”/transports the acyl groups of the growing chain through even FA synthesis. it needs CoA. (synth of CoA needs vit B5/pantothenic acid)

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15
Q

how do we go from one even FA cycle to another

A

malonyl-s-ACP binds to endprod (1st: butyryl-s-ACP) by condensation (s-s), forming a 6 carbon compound (leangtened by 2 carbons each cycle)

(Acetyl transacetylase enzyme is needed)

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16
Q

how many cycles of even FA synth. to synthesize palmitic acid?

A

n/2-1

16C/2 - 1 = 7 cycles (7 malonyl-CoA)

17
Q

differences of odd carbon FA synthesis

A

the reaction of making malonyl CoA is the only difference, methyl malonyl-CoA is made instead

18
Q

making unsaturated FA

A
  • cannot prod. double bond above delta9 →found in food, vitmins etc.
  • oleic acid (C18, delta9) and stearic acid (C18) can be made
19
Q

how are omega 6 FA’s made

A

omega 6 linoleic acid makes arachidonic acid

20
Q

how are omega 3 FA made

A

omega-3 linoleninc acid ⇒ EPA ⇒ DHA

(EPA and DHA are found in fish)

21
Q

prostanoids

A

Inflammation and blood clotting

  • *- good**: omega 3, decrease these
  • *- bad**: omega 6, increase these
22
Q

whats a good prostanoid

A

CLA: conjugated linolenic acid - polyunsaturated

  • anticancer
  • no CH2 btw doble bonds: -CH=CH-CH=CH-
  • ru: milk fat, plant origin
23
Q

where are trans FA found

A
  • ru milk fat
  • makes LDL (higher cholesterol and fats than VLDL)
  • no flexibility: no bend
24
Q

importance of ketogenesis

A
  • creates additional energy store using fat
  • used in time of starvation, diabetes, GI diseases
  • e.g. in early lactation of ru: incr. GNG
  • fuel for brain, heart, muscles
  • incr. ketogenesis ⇒ acidosis (ketonaemia, ketonuria(energy loss!))
25
Q

ketone body degradation

A

ketone bodies ⇒ AcCoA ⇒TCA⇒⇒⇒ glucose

26
Q

primary ketosis

A
  • huge amount of energy needed
  • diary ketosis: high yielding cows, GNG ⇒ use up OAC, accumilation of AcCoA
27
Q

secondary ketosis

A
  • not enough energy is taken up
  • starvation, GI diseases, diabetes (ketoacidosis, switch to FA burning since lack of insulin doesnt allow glucose to enter cell)