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
What happens to glycerol after lipolysis?
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
What happens to fatty acids after lipolysis?
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
What need to happen for ketone bodies to be formed?
Ketone bodies are formed when carbohydrate intake is inadequate and beta-oxidation product Acetyl CoA is in excess
28
What is the limiting factor in the citric acid cycle when glucose is low
When glucose is low, oxaloacetate is the limiting factor in the citric acid cycle, as it is converted to pyruvate on gluconeogenesis
29
What is converted into ketone bodies and what bodies does it form?
Acetyl CoA is converted to ketone bodies in the liver: 1) Acetoacetate 2) 3-hydroxybuterate 3) Acetone
30
What happens with ketone bodies in diabetes?
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
What must happen with excess protein?
Excess protein cannot be stored, so amino acids are oxidised for energy or converted to fat
32
What is transamination?
the process by which some amino acids can be converted to keto acids
33
What 2 things can happen to modified keto-acids after transamination?
1) generate pyruvate or keto-acid intermediates for the citric acid cycle 2) be converted to glucose via gluconeogenesis
34
What is deamination?
Deamination is the removal of an amine group (NH2) prior to oxidation or storage
35
What is the difference between a keto acid and ketone body?
A keto acid is an intermediate of the citric acid cycle Ketone body is a degradation stage of fatty acid oxidation
36
What does hepatic portal vein system ensure?
That the liver has ready access to absorbed nutrients
37
What are 2 major roles of the liver?
The liver is the major metabolism centre orchestrating interconversion of CHO, proteins, fats and lactate It also maintains blood glucose levels
38
What 3 things does resting muscle use as fuel
1) Fatty acids 2) Glucose 3) Ketone bodies