3.6 energy stores: glycogen and lipids Flashcards

(39 cards)

1
Q

where is glycogen stored

A

liver and muscles

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2
Q

what is the glycogen stored in liver used for

A

buffering blood glucose level

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3
Q

what is the glycogen stored in muscles used for

A

To provide glucose to generate energy during exercise

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4
Q

how does glucose form glycogen (simple details) (inclu. enzyme)

A

Moving the phosphate around, then adding the glucose to an existing glycogen chain using glycogen synthase

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5
Q

how does glycogen form glucose (simple details) (inc. enzyme)

A

To breakdown a glucose from glycogen, we use phosphorylase

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6
Q

why is glycogen metabolism controlled reciprocally

A
  • It is controlled reciprocally to prevent futile cycle

So only one side of the cycle is on at each time for energy efficient

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7
Q

2 methods of glycogen metabolism

A

allosterically and by hormones

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8
Q

3 molecules of allosteric control in glycogen metabolism

A

a. AMP (signals low enrgy levels)

b. Calcium (signals increased activity in muscles)

c. Glucose (signals enough energy)

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9
Q

2 hormones in glycogen metabolsim

A

insulin
glucagon

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10
Q

how does insulin work in glycogen metabolism

A
  • Released after a meal when blood glucose is high.
  • Activates phosphatases, promoting:

○ Glycogenesis (glycogen synthesis).

○ Inhibition of glycogenolysis (glycogen breakdown)

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11
Q

how does glucagon work in glycogen metabolism

A
  • Released during fasting or low blood glucose.
  • Activates kinases, promoting:

○ Glycogenolysis (glycogen breakdown).

○ Inhibition of glycogenesis (glycogen synthesis).

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12
Q

how does glucagon function

A
  • Glucagon act on a cell surface receptor of liver cells for:
  • Intracellular signal
  • Activation of a protein kinase which activates phosphorylase to breakdown glycogen into glucose
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13
Q

how does insulin function

A
  • Insulin opposes this effect by acting on its own cell surface receptors for:
  • A different intracellular signal that ultimately activates a protein that opposes kinases - phosphatase which activates glycogen synthase
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14
Q

diseases involved in aberrant fat handling/metabolism (and what species are affected)

A

obesity - all animals

pregnancy toxaemia - cows, sheep

hepatic lipidosis - cats, horses

diabetes - dogs, cats

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15
Q

what is the primary form of lipid storage

A

triacylglycerols (TAGS)

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16
Q

where is lipids stored (3)

A
  • adipose tissues
  • small amount in liver and muscles
17
Q

properties of TAGS

A

non-polar
non toxic
highly energy dense

18
Q

2 types of adipose tissue

A

white adipose tissue (WAT)
brown adipose tissue (BAT)

19
Q

properties of WAT (5)

A
  • Single fat droplet
  • Few mitochondria
  • Specialized to store triacylglycerol
  • Secretes multiple adipokines
  • Multiple anatomical depots
20
Q

properties of BAT

A
  • Multiple small fat droplets
  • Many mitochondria
  • Highly oxidative
  • Non-shivering thermogenesis for heat production (regulated by uncoupling proteins)
  • Smaller quantities of depots (e.g. periscapular depot)
  • Mostly observed in neonates (new born), smaller animals
21
Q

which 2 forms are lipids transported in blood as

A
  1. fatty acids (mostly bound to albumin)
  2. lipoproteins
22
Q

which organ is used for lipid metabolism

23
Q

what happens to the chylomicrons after transporting lipids to the liver

A

they become chylomicron remnants

24
Q

what happens to chylomicron remnants

A

they are processed in the liver to form VLDL, LDL, HDL

25
what are VLDL used for
Transport newly synthesized TAG from the liver to adipose tissue
26
what are LDL used for
carry a mixture of lipids around the body
27
what are HDL used for
Return lipid to liver from other tissues
28
what are the 5 types of lipase involved in hydrolyses of TAGS
- pancreatic lipase - lipoprotein lipase - adipose triglyceride lipase - adipose hormone sensitive lipase - adipose monoacyglycerol lipase
29
what are the uses of the 5 types of lipase
30
process of lipolysis
- Fatty acids are oxidized in the mitochondria of active tissues to produce ATP (requires oxygen) - Important in active tissues ○ e.g. skeletal muscle - Oxidation occurs in the mitochondrial matrix - Requires transport of activated fatty acids molecules across the mitochondrial membrane, which is a controlled process (acyl carnitine via CPT1 transporter) ○ It is inhibited by malonyl-CoA which is intermediate in fatty acid synthesis - the use reciprocal regulation - Activated fatty acids = fatty acyl CoA - Once in the mitochondrial matrix, fatty acyl CoA is broken down by the repeated removal of 2-carbon fragments as acetyl CoA ○ This process is beta-oxidation Palmitate (a fatty acid with 16 carbons), it undergoes 7 cycles, each cycle removing 2 carbons as acetyl CoA, this results in 8 acetyl CoA
31
where does fatty acid synthesis occurs mostly
liver and adipose tissues
32
process of fatty acid synthesis
- Fatty acids are synthesized from acetyl CoA when energy is abundant - - Synthesis occurs by repeated condensation of 2 carbon units to build up an even numbered long chain of fatty acids - Synthesis cannot occur by reversing the B-oxidation breakdown pathway ○ It uses unique path with some unique enzymes and occurs in cytosol Thus reciprocal regulation
33
what enzyme is involved in fatty acid synthesis
acetyl CoA carboxylase (ACC)
34
how is ACC inhibited and activated
inhibit: glucagon and adrenaline activate: insulin
35
what does malonyl CoA do
inhibit CPT 1 and thus transport of acyl CoA into mitochondria for breakdown
36
what is the 16 C lipid called
palamitate
37
why would ACC release the lipid when it gets to 16C
When the chain is 16 C long (palmitic acid), it becomes too big for the enzymes and is released
38
what is lipogenesis
Lipogenesis = building fats
39
what is adipogenesis
Adipogenesis = expansion of adipose tissue