Biochemistry Flashcards

1
Q

what cells make up the pancreatic islet?

A

alpha cells
beta cells
delta cells
PP cells

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2
Q

what does it secrete:

alpha cells

A

insulin

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3
Q

what does it secrete:

beta cells

A

glucagon

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4
Q

what does it secrete:

delta cells

A

somatostatin

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5
Q

what does it secrete:

PP cells

A

pancreatic polypeptide

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6
Q

the insulin peptide structure has _ polypeptide chains linked by what type of bond?

A

the insulin peptide structure has 2 polypeptide chains linked by DISULFIDE BONDS

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7
Q

name the type of insulin that is…

ultra fast/ultra short acting

A

lispro

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8
Q

name the type of insulin that is…

short-acting

A

regular

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9
Q

name the type of insulin that is…

intermediate acting

A

NPH/lente

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10
Q

name the type of insulin that is…

long acting

A

ultralente

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11
Q

name the type of insulin that is…

ultra long acting

A

glargine

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12
Q

insulin lispro is ____meric

A

insulin lispro is MONOmeric

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13
Q

glargine is administered at what time of the day?

A

bedtime

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14
Q

glucose enters _ cells through the _____ glucose transporter and is phosphorylated by ___________

A

glucose enters BETA cells through the GLUT2 glucose transporter and is phosphorylated by GLUCOKINASE

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15
Q

Increased metabolism of glucose leads to an increase in intracellular ___ concentration

A

Increased metabolism of glucose leads to an increase in intracellular ATP concentration

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16
Q

how many ATP are produced per glucose?

A

36

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17
Q

glucose-6-P -> __________ -> acetyl-CoA -> ___ cycle

A

glucose-6-P -> GLYCOLYSIS -> acetyl-CoA -> TCA cycle

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18
Q

ATP inhibits what channel?

A

K+ channel

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19
Q

inhibition of the K+ channel leads to hyper/depolarisation of the cell membrane

A

inhibition of the K+ channel leads to DEPOLARISATION of the cell membrane

20
Q

depolarisation of the cell membrane results in opening of what channel?

A

voltage gated Ca2+ channel

21
Q

increase in internal Ca2+ concentration leads to release of what?

22
Q

insulin should only be secreted in response to blood glucose rising above what?

23
Q

in T1DM, beta cells are….

24
Q

release of insulin is __phasic

A

release of insulin is BIphasic

25
sulphonylurea drugs mimic the action of ___ to depolarise ____ cells
sulphonylurea drugs mimic the action of ATP to depolarise BETA cells
26
Kir6 and SUR1 are 2 proteins that make up what channel?
Katp channel
27
Kir6.2 mutations can lead to _________ diabetes
Kir6.2 mutations can lead to NEONATAL diabetes
28
some Kir6.2 or SUR1 mutations lead to congenital _________________
some Kir6.2 or SUR1 mutations lead to congenital HYPERINSULINISM
29
monogenic diabetes with genetic defect in b cell function familial form of early-onset type II diabetes, primary defects in insulin secretion mutations in at least 6 different genes (150 different mutations) can cause diagnosis?
MODY
30
activity of what is impaired in MODY2?
glucokinase activity
31
MODY is treated with ______________ whereas T1DM is treated with _______
MODY is treated with SULPHONYLUREA whereas T1DM is treated with INSULIN
32
loss of insulin secreting beta cells diagnosis?
T1DM
33
defective glucose sensing in the pancreas and/or loss of insulin secretion diagnosis?
MODY
34
initially hyperglycemia with hyperinsulinemia so primary problem is reduced insulin sensitivity in tissues diagnosis?
T2DM
35
biological effect of insulin: 1. Amino acid uptake in muscle 2. Lipolysis 3. DNA synthesis 4. Protein synthesis 5. Growth responses 6. Glucose uptake in muscle and adipose tissue 7. Gluconeogenesis in liver 8. Lipogenesis in adipose tissue and liver 9. Glycogen synthesis in liver and muscle what's turned on and whats turned off?
1. Amino acid uptake in muscle - ON 2. Lipolysis - OFF 3. DNA synthesis - ON 4. Protein synthesis - ON 5. Growth responses - ON 6. Glucose uptake in muscle and adipose tissue - ON 7. Gluconeogenesis in liver - OFF 8. Lipogenesis in adipose tissue and liver - ON 9. Glycogen synthesis in liver and muscle - ON
36
name the type of receptor that insulin binds to
receptor tyrosine kinase
37
rare autosomal recessive genetic trait mutations in the gene for the insulin receptor severe insulin resistance developmental abnormalities: - elfin facial appearance - growth retardation - absence of subcutaneous fat, decreased muscle mass caused by defects in insulin binding or insulin receptor signalling diagnosis?
leprechaunism – Donohue syndrome
38
rare autosomal recessive genetic trait severe insulin resistance, hyperglycemia and compensatory hyperinsulinemia developmental abnormalities acanthosis nigricans (hyperpigmentation) fasting hypoglycaemia (due to hyperinsulinemia) diabetic ketoacidosis Ssevere cases linked to mutations in the insulin receptor that reduce sensitivity diagnosis?
Rabson Mendenhall syndrome
39
vomiting dehydration increased heart rate distinctive smell on breath diagnosis?
diabetic ketoacidosis - DKA
40
where are ketone bodies formed?
liver mitochondria
41
in T1DM, DKA is a danger is insulin supplementation is ______
in T1DM, DKA is a danger is insulin supplementation is MISSED
42
DKA is more rare in T_DM
DKA is more rare in T2DM
43
if supply of ____________ is limited (eg no glycolysis) the Acetyl CoA diverted to ketones
if supply of OXALOACETATE is limited (eg no glycolysis) the Acetyl CoA diverted to ketones
44
when glucose is not available, what are oxidised to provide energy?
fatty acids
45
accumulation of ketone bodies leads to what?
acidosis