Metabolic Stores Flashcards

1
Q

What is metabolism?

A

Mechanisms which couple the demand for energy with the fuel supply

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2
Q

What does insulin promote?

A
  • glucose uptake
  • Fatty acid synthesis
  • Protein synthesis
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3
Q

What is the absorptive/fed state?

A

nutrients are plentiful - fuels broken down and excess stored the aim is to store nutrients in mobilizable form for times of need

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4
Q

What is the postabsorptive/ fasting state?

A

Storage molecules broken down for energy; the aim is to provide metabolites for cellular respiration synthesis and maintain blood glucose levels within homeostatic range

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5
Q

What effector organs control interconversion?

A
  • Liver
  • Adipose
  • Muscle
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6
Q

Where does blood glucose come from in the postabsorptive state?

A

Glycogenolysis:
Liver glycogen ~100g (enough for ~3 – 5 hours activity)
Muscle glycogen (only utilised within muscle)

Gluconeogenesis (formation of glucose from noncarbohydrate molecules):

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7
Q

What is glycogen and where is it stored?

A

A branched polysaccharide storage molecule for glucose

Liver and skeletal muscle are the main glycogen reservoirs

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8
Q

How does the liver store glycogen?

A

maintains blood glucose levels
Enough glycogen for 3 – 5 hours moderate exercise, or
12 hours overnight fast

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9
Q

How does the muscle store glycogen?

A

stores glycogen for muscle contraction only

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10
Q

Describe glycogenesis

A

promoted by insulin

Glucose → G-6-P → G-1-P → Glycogen

Glucose residues formed by α1,4-glycosidic linkages

Branching occurs via α1,6-glycosidic linkages

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11
Q

Describe glycogenolysis

A

promoted by glucagon, adrenalin, cortisol and growth hormone

In muscle, no glucagon receptors – responds mainly to adrenalin

Two enzymes required:
Glycogen phosphorylase - α1,4 linkages
Debranching enzyme – α1,6 linkages

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12
Q

What breaks down glycogen in the muscle

A

No G-6-Pase enzyme, G-6-P enters glycolysis

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13
Q

What fuel sources can be mobilised?

A

1) Glucose
2) Triglycerides
3) Amino acids

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14
Q

What promotes glycogenesis?

A

Insulin

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15
Q

How does glycogenesis occur?

A

Glucose to G-6-P to G-1-P to Glycogen

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16
Q

How are glucose residues formed?

A

Glucose residues are formed by α 1,4 glycosidic linkage

17
Q

How long do glycogen stores last?

A

Glycogen stores last about 3-5 hours

18
Q

What are lipid?

A

Major form in which energy is stored

19
Q

How much more energy can triglycerides produce than glycogen

A

triglycerides (triacylglycerols) can produce about 6 times as much energy as glycogen

20
Q

What substances can be used in gluconeogenesis?

A

1) Glycerol from triglycerides
2) Glucogenic amino acids (alanine and glutamine)
3) Lactate

21
Q

What tissues have glucose as their primary source of energy?

A

1) Brain
2) Red blood cells
3) Renal medulla
4) Lens

22
Q

Where does gluconeogenesis occur?

A

Gluconeogenesis takes place mainly in the liver

It can also take place in the kidneys in prolonged fasting

23
Q

What enzymes are required for gluconeogenesis?

A

1) Pyruvate carboxylase (mitochondria)
2) Phosphoenol pyruvate carboxykinase (mitochondria + cytosol)
3) Glucose-6-Phosphatase (ER

24
Q

What lipolysis?

A

Lipolysis is fat breakdown into glycerol and fatty acids (reverse of lipogenesis)

25
Q

What happens to glycerol after lipolysis?

A

1) Glycerol
* Glycerol feeds into gluconeogenesis, but can also be utilised by most cells
* It can be converted into glyceraldehyde-3-phosphate (glycolysis intermediate), which can enter into glycolysis, which results in 15 ATP generated aerobically

26
Q

What happens to fatty acids after lipolysis?

A

Fatty acids
* Fatty acids undergo β-oxidation
* They are broken down into Acetic acid (2C) and fused to coenzyme A to form Acetyl CoA
* This process reduces FAD and NAD+, which can then be fe into the ETC
* Acetyl CoA can then enter the citric acid cycle

27
Q

What need to happen for ketone bodies to be formed?

A

Ketone bodies are formed when carbohydrate intake is inadequate and beta-oxidation product Acetyl CoA is in excess

28
Q

What is the limiting factor in the citric acid cycle when glucose is low

A

When glucose is low, oxaloacetate is the limiting factor in the citric acid cycle, as it is converted to pyruvate on gluconeogenesis

29
Q

What is converted into ketone bodies and what bodies does it form?

A

Acetyl CoA is converted to ketone bodies in the liver:

1) Acetoacetate
2) 3-hydroxybuterate
3) Acetone

30
Q

What happens with ketone bodies in diabetes?

A

In diabetes, acetoacetate is produced faster than it is metabolised
This results in ketone bodies accumulating in the blood (potential acidosis) and fruity smell of acetone on the breath

31
Q

What must happen with excess protein?

A

Excess protein cannot be stored, so amino acids are oxidised for energy or converted to fat

32
Q

What is transamination?

A

the process by which some amino acids can be converted to keto acids

33
Q

What 2 things can happen to modified keto-acids after transamination?

A

1) generate pyruvate or keto-acid intermediates for the citric acid cycle
2) be converted to glucose via gluconeogenesis

34
Q

What is deamination?

A

Deamination is the removal of an amine group (NH2) prior to oxidation or storage

35
Q

What is the difference between a keto acid and ketone body?

A

A keto acid is an intermediate of the citric acid cycle
Ketone body is a degradation stage of fatty acid oxidation

36
Q

What does hepatic portal vein system ensure?

A

That the liver has ready access to absorbed nutrients

37
Q

What are 2 major roles of the liver?

A

The liver is the major metabolism centre orchestrating interconversion of CHO, proteins, fats and lactate
It also maintains blood glucose levels

38
Q

What 3 things does resting muscle use as fuel

A

1) Fatty acids
2) Glucose
3) Ketone bodies