Carbohydrate metabolism Flashcards

1
Q

What is hypoglycaemia and what are the symptoms

A

Low levels of glucose causing muscle weakness, loss of coordination, mental confusion, sweating and in worst cases coma and death

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2
Q

What is hyperglycaemia and what are the symptoms

A

High levels of glucose causing non enzymatic modification of proteins (cataracts and lipoproteins)

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3
Q

What affects blood glucose

A

Intake of glucose increases blood glucose concentration vastly and it will gradually fall back down
Exercise doesn’t affect blood glucose level

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4
Q

Where and how is excess glucose stored

A

Liver is the main storage of glucose

Its stored as glycogen

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5
Q

Why is this storage molecule efficient

A

Its highly branched so enzymes can easily break it down for quick access to the glucose
Glycogen doesn’t affect water potential therefore it doesn’t draw in large quantities of water

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6
Q

What is the structure of glycogen

A

Glycogen includes alpha 1-4 which are straight bonds and alpha 1-6 which allows branching

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7
Q

What enzymes are involved in the formation of glucose

A

glycogen synthase and a branching enzyme

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8
Q

Glycogen synthesis

A
  1. Glucose 6 phosphate is made into glucose 1 phosphate by phosphoglucomutase
  2. This is then activated by UTP (uridine triphosphate) to create UPD-glucose and Pi as a bi product, this is done UDP-glucose-pyrophosphorylase
  3. UDP-glucose attaches to glycogenin
  4. Glycogen synthase increases the chain length to 11 residues
  5. At 11 residues the branching enzyme forms an alpha 1-6 bond, therefore extending the molecule creating branches
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9
Q

Why glycogen and not fat

A

Fat can not be mobilised as readily
Fat cannot be used as an energy source in the absence of oxygen
Fat cannot be converted in to glucose

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10
Q

What enzymes are involved in glycogen breakdown

A
Phosphorylase breaks alpha 1-4 links 
Translocase 
De-branching enzyme alpha 1-6 
Phosphoglucomutase converts G1P to G6P 
Glucose 6 phosphatatse converts G6P to glucose
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11
Q

What is glycogen phosphorylase

A

A key enzyme in glycogenolysis to form glucose-1-phosphate
An allosteric enzyme activated by phosphorylation but modulated by other factors
Inactive - phosphorylase b
Active - phosphorylase a

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12
Q

How is glycogen phosphorylase regulated

A
  1. ATP is made into cyclic AMP through adenylate cyclase
  2. This activates protein kinase A
  3. Which activates phosphorylase kinase
  4. This phosphorylates phosphorylase b into phosphorylase a
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13
Q

What hormones regulate glycogenolysis

A

Insulin inhibits
Glucagon stimulates in the liver
Adrenaline stimulates in the muscle
Cortisol is weak stimulus

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14
Q

How is phosphorylase regulated in muscle

A

Can be activated by 5’-AMP without being phosphorylated
5’-AMP is formed when ATP is depleted
ATP and G-6-P can block 5’-AMP activation
ATP binds on the same site

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15
Q

How is phosphorylase regulated in the liver

A

Phosphorylase a is inhibited by glucose

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16
Q

How is phosphorylase b activated in muscle and liver

A

Ca2+ ions activate phosphorylase b during muscle contraction, you only get maximum activity with phosphorylation and Ca2+ activation
In liver, alpha adrenergic activation stimulates Ca2+ release

17
Q

When and how is glycogen synthase regulated

A

Activated when glucose is in large supply
Activated though ATP and G6P
Its inactivated by phosphorylation by protein kinase A
Its deactivated by dephosphorylation by protein phosphatase-1

18
Q

When and how is glycogen phosphorylase regulated

A

Activated when glucose is in short supply
Inactivated by ATP and G6P
Activated by phosphorylation by phosphorylase b kinase
Inactivated by dephosphorylation by protein phosphatase-1

19
Q

What does the pentose phosphate pathway do

A

Generates ribose 5 phosphate and NADPH

20
Q

Whats NAPDH used for

A

required for fatty acid synthesis when there is excess circulating glucose

21
Q

Why would this pathway be reversed

A

When the body needs to build up its circulating glucose levels