Insulin Secretion and signalling Flashcards

1
Q

Where is insulin made?

A

Pancreatic islets

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2
Q

What types of cells pancreatic islets and what do they secrete?

A

beta cells - insulin
alpha cells - glucagon
delta cells - somatostatin
PP cells - pancreatic polypeptide

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3
Q

What is the structure of insulin?

A

2 polypeptidechains
linked by disulfide bonds
connecring (C) peptide

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4
Q

How does glucose enter beta cells?

A

through GLUT2 transporter

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5
Q

What happens when glucose enters the beta cell?

A
Phosphorylated by glucokinase
Increases intracellular ATP
ATP inhibits K ATP channel
Depolarisation
Voltage gated Ca2+ channels open
Vesicles fuse to membrane
Secrete insulin
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6
Q

Desribe the two phases of insulin secretion

A

1st-readily releasable pool

2nd- mobilization

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7
Q

What subunits make up the K ATP channel? What inhibits each subunit?

A

Kir6.2 pore - ATP

SUR1 regulatory - sulphonylurea

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8
Q

What stimulates the K ATP channel at the SUR1 subunit?

A

diazoxide

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9
Q

Describe what the defect in MODY

A

Glucokinase impared
Glucose sensing defect
Increases threshold for insulin secretion

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10
Q

What are the three phases of the signalling cascade?

A

Reception of hormone
Transduction
Cellular response

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11
Q

What is the name of the insulin receptor?

A

Tyrosine kinase

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12
Q

Describe the tyrosine kinase receptor

A

2 alpha subunits
2 beta subunits
disulfide bridges

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13
Q

Describe what happens in insulin signalling

A

Insulin binds to alpha subunits
Autophosphorylation at beta subunits
Insulin receptor substrates phosphorylated
Causes gene expression and glycogen synthesis

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14
Q

Describe how glycogen is synthesised

A

PKB causes GLUT4 to translocate to surface

Glucose into cell

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15
Q

What are the biological processes insulin increases?

A

Glucose uptake
Lipogenesis
Glycogen synthesis

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16
Q

What biological processes does insulin prevent?

A

Lipolysis

Gluconeogenesis in liver

17
Q

What happens in Donohue syndrome (leprachaunism)

A

insulin resistance
growth abnormlities
elfin features
growth retardation

18
Q

What happens in Robson Mendenhall syndrome?

A
insulin resistance 
hyperglycaemia 
compensatory hyperinsulinaemia
leads to: hyperpigmentatoin
DKA hypoglycaemia respone
19
Q

Where are ketone bodies produced?

A

liver mitochondira

20
Q

When are ketone bodies formed?

A

fatty acids oxidised in TCA cycle

excess acetyl co-A turned to ketone bodies

21
Q

Name three ketone bodies

A

Acetone
Acetoacetic acid
Beta-hydroxybutyric acid

22
Q

When is ketoacidosis most common?

A

Type 1 diabetes