Carbohydrate Metabolism Flashcards

1
Q

What is the critical blood glucose level?

A

2.5 mM

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2
Q

What are the symptoms of hypoglycaemia?

A
Muscle weakness
Loss of coordination
Mental confusion
Sweating 
Hypoglycaemic coma and death
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3
Q

What are the hyperglycaemic symptoms?

A

Non enzymatic modification of proteins which could lead to cataracts
Hyperosmolar coma

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4
Q

What is glycogensis

A

Glycogen synthesis

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5
Q

How much glycogenesis takes place (in grams) in the liver and skeletal muscle?

A

100g in liver

300-400g in skeletal muscle

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6
Q

When does glycogenesis take place?

A

When blood glucose levels are high

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7
Q

What is glycogen?

A

Branched polymer of glucose

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8
Q

How is glycogen formed?

A

Alpha 1-4 and 1-6 glycosidic bonds

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9
Q

Where is glycogen formed

A

On a protein primer called glycogenin

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10
Q

What is glycogenesis regulated by?

A

Glycogen synthase

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11
Q

How are the branched points formed?

A

by a branching enzyme

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12
Q

What enzyme performs G6P-G1P

A

Phosphoglucomutase

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13
Q

What enzyme performs G1P+UTP->UDP

A

UDP glucose pyrophosphorylase

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14
Q

What enzyme adds more glucose residues to the glycogenin?

A

Glycogen synthase

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15
Q

How long is the original glycogen chain before branching happens?

A

11 glucose residues

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16
Q

Why is glycogen formed?

A

Glucose is osmotically active so it cant be stored (affects the water potential of the cells)

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17
Q

What is glycogenolysis?

A

Glycogen breakdown

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18
Q

Where does glycogenolysis happen?

A

Liver, muscle and (sometimes) kidney

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19
Q

When does glycogenolysis happen?

A

When glucose levels are low

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20
Q

What is glycogenolysis stimulated by?

A

Glucagon, Adrenaline, noradrenaline, growth hormone

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21
Q

What enzyme breaks the 1-4 glycosidic bonds between the glucose residues?

A

Phosphorylase

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22
Q

What does the breakdown of 1-4 glycosidic bonds produce?

A

G1P

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23
Q

What does phosphoglucomutase facilitate?

A

G1P-G6P

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24
Q

What enzyme removes the last 3 glucose residues on a branch?

A

Transferase

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25
Where do the last 3 glucose residues go when they are debranched?
Added to the non-reducing end of the chain
26
What enzyme breaks the 1-6 glycosidic bonds?
Alpha 1-6 glucosidase
27
What happens to the glucose when it is freed from the glycogen?
Phosphorylated by hexokinase in the muscle to form G6P
28
What breaks down the glucose chains to produce G1P?
Phosphorylase
29
In the liver what enzyme does the G6P->glucose reaction?
G6-phosphatase
30
What are the products of glycolysis?
G1P, glucose
31
What is glycogen phosphorylase?
Large multi-subunit enzyme that plays a key role in glycogenolysis
32
What is glycogen phosphorylase regulated by?
Allosteric interactions that signal the energy state of the cell
33
What are the two isoforms of glycogen phosphorylase?
Active - phosphorylase A | Inactive - phosphorylase B
34
What is phosphorylase A phosphorylated by?
Phosphorylase B kinase
35
What inhibits phosphorylase?
Insulin
36
What stimulates phosphorylase in the liver?
Glucagon
37
What stimulates phosphorylase in the muscle?
Adrenaline
38
What weakly stimulates phosphorylase?
Cortisol
39
In muscle what can glycogen phosphorylase B be activated by?
5’AMP
40
What blocks 5’ AMP activation?
ATP and G6P
41
In the liver what is phosphorylase A inhibited by?
Glucose
42
When and how is glycogen synthase activated?
In times of plenty of glucose, by insulin
43
When and how is glycogen phosphorylase activated?
When blood glucose is low, by glucagon, adrenaline and noradrenaline
44
What does the pentose phosphate pathway start and end with?
Starts with G6P and ends with ribose 5 phosphate
45
What is ribose 5 phosphate included in?
Nucleotide and Nucleic acid synthesis
46
Where is NADPH formed?
In the pentose phosphate pathway
47
What is GSH used in?
In the protective mechanism of the self and to oxidative stress
48
What is NADPH important to?
The formation of GSH and fatty acids
49
What molecules do gluconeogenesis?
Triglycerides Lactate Amino acids
50
What is gluconeogenesis?
Creation of new glucose
51
Where does gluconeogenesis take place?
Mainly in the liver and the kidney, but also a bit in the intestine
52
When does gluconeogenesis take place?
When the blood glucose levels are very low (fasting or starving)
53
What is gluconeogenesis the reverse of?
Glycolysis
54
What enzyme takes pyruvate to oxaloacetic acid?
Pyruvate carboxylase
55
What enzyme takes oxaloacetic acid to phosphoenol pyruvate?
Phosphoenol pyruvate carboxykinase
56
What enzyme reverses phosphofructokinase?
Fructose 1-6 bisphosphate
57
What enzyme reverses hexokinase?
Glucose-6-phosphatase
58
Where are the fatty acids fed into the TCA cycle?
Glycerol components feed in where F1-6 bisphosphate is split
59
Where is pyruvate synthesised?
In the cytosol
60
Where does pyruvate carboxylase work?
In the mitochondria
61
3 most important substrates are
Amino acids (Alanine) Lactate Glycerol from triglycerides
62
What is gluconeogenesis used for?
To maintain blood glucose
63
What is the daily requirement for blood glucose?
160g
64
What is the daily requirement for blood glucose in the brain?
120g
65
What are the total body reserves of glucose?
210g
66
What does the gluconeogenic pathway do?
Pyruvate to glucose
67
Where does the gluconeogenic pathway take place?
Mostly in the liver and a little in the kidney
68
Where does the gluconeogenic pathway take place during starvation?
Kidney productions rise to 40% and a little in the liver