Lipids Flashcards

1
Q

What are the essential FA?

A

linoleic and alpha-linolenic - form prostaglandins and omega 3 & arachidonic acid

Arachidonic acid essential IF linoleic acid deficient to lin. acid can’t form arach. - form eicosanoids

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2
Q

What does omega 3 do?

A

Lowers plasma cholesterol and lowers high blood pressure

Deficiency - depression and ADHD

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3
Q

What are the dietary lipids?

A

TAG!! phospholipid, cholesterol, cholesterol ester and free FA

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4
Q

Outline digestion of TAG

A
  1. Broken down by pancreatic lipase - FA cleaved
  2. Bile emulsifies fat and products formed mixed MICELLES with bile salts
  3. Go to microvilli and lipid products released and move through diffusion

Short and medium chain FA do not require micelles

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5
Q

How are lipids transported after be digested?

A
  1. Intestinal cells resynthesize TAG and then apoB-48 packages them in chylomicrons
  2. Released by exocytosis to lymph then blood
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6
Q

What happens when chylomicrons reach tissue?

A
  1. TAG hydrolysed to FA and glycerol by lipoprotein lipase
  2. FA used for energy or resynthesises to TAG for storage
    Glycerol can be taken liver to produce glycerol-3-phosphate for glycolysis and gluconeogenesis
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7
Q

How is FA released from TAG in tissue?

A

Hormone sensitive lipase (HSL) - HSL activated by epinephrine (flight or flight adrenaline)

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8
Q

List the different lipoproteins

A
  • Chylomicrons: TAG - intestine to tissue
  • VLDL - TAG: liver to tissue
  • LDL - chol: liver to tissue -BAD
  • HDL - chol: tissue to liver -GOOD

Can also be transported by serum albumin

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9
Q

What is beta-oxidation of FA, where does it occur and what does it produce?

A
  • Catabolism of FA
  • Mitochondrial matrix
  • Acetyl CoA, FADH2 AND NADH
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10
Q

In simple terms, what are the 3 steps in beta oxidation?

A
  1. Activation in the cytosol (needs ATP) - fatty acyl CoA
  2. Transport to the mito. matrix
  3. Degradation to 2 Acetyl CoA to be used for energy
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11
Q

What is the carnitine shuttle?

A

Transports FA INTO mito. matrix - transports RC=O and once inside matrix, breaks down as RC=O resynthesised to fatty acyl CoA and carnatine goes back to cytosol

ONLY REQUIRED FOR LONG FA CHAIN - SHORT AND MEDIUM ARE CAT INDEPENDENT

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12
Q

What prevents FA synthesis and beta oxidation from occurring simultaneously?

A

Malonyl CoA - inhibits carnitine palmitoyl transferase

Deficiency - no B-oxidation, so glucose stores used - hypoglycaemia
Treat - give medium chain that does not need CAT-1 for transport

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13
Q

What are ketone bodies and what is their role?

A

Made from excess Acetyl CoA in mito. matrix in liver cells and used as fuel for cardiac and skeletal muscle

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14
Q

Problem of excess ketone bodies

A

Uncontrolled diatbetes or starvation leads to high levels as FA broken down to replace - causes KETONEMIA (blood), KETONURIA (urine) and ACADEMIA - breath has fruity odour due to acetone

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15
Q

What are FA derived from what does in require?

A

Acetyl CoA and needs ATP and NADPH

Occurs in cytosol

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16
Q

What is the citrate shuttle?

A

Transport Acetyl CoA from matrix to cytosol

  1. Citrate synthase binds to oxaloacetate and acetyl CoA to form citrate
  2. Citrate lyase breaks it up in cytosol
17
Q

Outline of steps in FA

A

Acetyl CoA –> Malonyl CoA –> Palmitic Acid

First steps uses Acetyl CoA Carboxylase

18
Q

What is role of cholesterol?

A

In cell membrane and precursor for sterol hormones, Vit D and bile salts

19
Q

Role of statin

A

Lowers LDL level

20
Q

Role of eicosanoids

A

Precursor for prostaglandins, thromboxanes and leukotrienes

Inflammatory response - pain and fever, blood pressure, blood clotting etc

21
Q

What are COX inhibitors

A

Non-steroidal anti-inflammatory drugs (NSAIDs)

Inhibit COX synthesis of inflammatory prostaglandins