Biochemistry Flashcards

1
Q

What do beta cells secrete?

A

insulin

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2
Q

What do alpha cells secrete?

A

glucagon

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3
Q

What do omega cells secrete?

A

Somatostatin

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4
Q

What do PP cells secrete?

A

Pancreatic polypeptide

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5
Q

What does insulin contain?

A

2 poly peptide chains linked by disulfide bonds

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6
Q

How does glucose enter beta cells?

A

through the GLUT2 glucose transporter, its phosphorylated by glucokinase

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7
Q

What does ATP inhibit?

A

ATP-sensitive K+ channel K(ATP)

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8
Q

What does inhibition of K(ATP) lead to?

A

Depolarisation of the cell membrane

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9
Q

What does cell membrane depolarisation lead to?

A

Opening of voltage-gated Ca2+ channels

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10
Q

What does an increase in internal Ca2+ conc lead to?

A

fusion of secretory vesicles with the cell membrane and release of insulin

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11
Q

What’s the subunit of inward rectifier subunit (K(IR))?

A

Kir6.1

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12
Q

What’s the subunit of a sulphonylurea receptor?

A

SUR1

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13
Q

Loss of insulin secreting beta cells is what type of diabetes?

A

1

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14
Q

Defective glucose sensing in the pancreas and/or loss of insulin secretion is what?

A

MODY

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15
Q

Initially hyperglycaemia with hyperinsulinemia so primary problem is reduced insulin sensitivity in tissues is what?

A

Type 2 diabetes

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16
Q

Describe the insulin receptor?

A

A dimeric tyrosine kinase
Two extracellular alpha subunits with insulin binding domains
Two transmembrane beta subunits
Linked by disulfide bonds

17
Q

What happens to beta cells when alpha cells bind to insulin?

A

They self phosphorylate (autophosphorylation)

18
Q

What is Leprechaunism (Donohue Syndrome)?

A

rare autosomal recessive genetic trait
Mutations in gene are for insulin receptor
Severe insulin resistance

19
Q

What are features of Donohue syndrome?

A

Elfin facial expression
Growth retardation
Absence of subcutaneous fat, decreased muscle mass

20
Q

What is Rabson Mendenhall syndrome?

A
rare autosomal recessive 
Sever insulin resistance 
hyperglycaemia, hyperinsulinemia
Developmental problems
Acanthosis nigricans (hyperpigmentation)
21
Q

Where are ketone bodies formed?

A

In liver mitochondria

derived from acetyl-CoA from beta oxidation

22
Q

When are ketone bodies converted back to acetyl-CoA?

A

When they renter the TCA cycle

23
Q

Ketoacidosis is associated with which diabetes type?

A

1