Chapter 24 Flashcards

1
Q

Digestion of triglycerides

A
  1. separated into small droplets
  2. bile acids and pancreatic lipases hydrolyze fats to free fatty acids & mono/di-glycerides
  3. abdorbed into the blood & attached to serum albumin
  4. absorbed into the intestinal cells and packaged into lipoproteins
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2
Q

Bile

A

Fluid released from the gall bladder to digest the foods we eat.

  • made in the liver
  • stored in the gall bladder
  • emlusifying agent

(cholic acid is the major bile acid)

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3
Q

chylomicrons

A

partiallt digested mono and diglycerides absorbed and recomined into triglycerides and packaged into lipoproteins

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4
Q

Lipid transport

A

enter metabolism through three different sources:

  1. diet ( transported by chylomicrons)
  2. storage in adipose tissue (transported by serum albumin)
  3. synthesis in the liver ( transported by VLDLs)
  4. cholesterol from liver ( transported by LDLs)
  5. cholesterol form dead cells( tranported by HDLs)

​Must eventually be transported in blood (in a carrier system)

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5
Q

lipoproteins

A

micelle that conatins trigylcerides and cholesterol.

  1. phospholipid
  2. protein around the surface
  3. cholesterol and cholesterol ester
  4. trigylceride
  • Transport both fat and cholesterol
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6
Q

lipoprotein density

A

Mostly hydrocarbon, greater the fat the lower the density

  1. chylomicrons (lowest density)
  2. VLDLs (very low density lipoproteins)
  3. IDLs (intermediate density lipoproteins)
  4. LDLs (low density lipoproteins)
  5. HDLs (high density lipoproteins)
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7
Q

Good and bad cholesterol

A
  • HDLs are called good cholesterol
  • LDLs are called bad cholesterol

There is no such thing as good or bad cholesterol

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8
Q

Storage of trigylcerides

A

Stored in adipocytes

  • fat must be disassembled to cross membranes
  • after a meal insulin activates the synthesis of trigclycerides for storage
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9
Q

oxidation of fatty acids

A
  1. activation → by CoA
  2. transport→mitochondrial matrix
  3. oxidation →oxidized to produce acetly-CoA, NADH and FADH2

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10
Q

ß oxidation pathway

A

Purpose:

  1. oxidize fatty acids
  2. cut fatty acid into 2-Carbon pieces

Starting materials:

  • Fatty acid-SCoA
  • Free CoA,NAD+,FAD

Products:

  • acetyl-CoA
  • NADH, FADH2
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11
Q

triacylgycerol metabolism

A

only recognize triacylgycerol pathway

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12
Q

Thromboxane

A
  • promotes blood clotting
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13
Q

Sphingomyelin

A
  • forms cell membrane
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14
Q

ketogenisis

A

Synthesis of ketone bodies from acetyl-CoA

_Purpose: _

recycle acetyl-CoA back to free CoA

SM: 2 acteyl-CoA; Products: 2 free Co, 1 acetoacetate

Ketone bodies:

  • when there is too much acetyl-CoA for the citric acid cycle to process ketone bodies are formed
  • produced in the liver that can be used as fuel by msucles and the brain
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15
Q

lipogensis

A

synthesis of fatty acids from acetyl-CoA

  • occurs in the cytoplasm
  • when there is an excess of acetly-CoA
  • regulated by insulin and glucagon
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