Insulin and diabetes drugs Flashcards

1
Q

insulin MoA

A

lowers blood glucose by stimulating peripheral glucose uptake primarily by skeletal muscle cells and fat, and by inhibiting glucose production and release by the liver.

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2
Q

insulin adverse effects

A

hypoglycemia

lipodystrophy

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3
Q

insulin contradictions

A

renal impairment

patients at risk of hypoglycaemia

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4
Q

insulin drug interactions

A
  • Dose needs increasing with systemic steroids

- Caution with other hypoglycaemic drugs

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5
Q

name a biguinide

A

metformin

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6
Q

biguinide MOA

A

↓hepatic glucose production by inhibiting gluconeogenesis; some gluconeogenic activity remains so hypoglycaemia risk reduced

Supress appetite so limit weight gain

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7
Q

biguinide adverse effects

A

GI upset

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8
Q

biguinide contradictions

A
  • Excreted unchanged by kidneys so stop if eGFR < 30 mL/min

- Alcohol intoxication

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9
Q

biguinide drug interactions

A
  • ACEi, diuretics, NSAIDs (drugs that may impair renal function)
  • Loop and thiazide like diuretics ↑glucose so can reduce metformin action
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10
Q

name a sulfonylurea

A

gliclazide

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11
Q

sulfonylurea MoA

A

Stimulate β-cell pancreatic insulin secretion blocking ATP-dependant K+ channels

Need residual pancreatic function to work; weight gain through anabolic effects of insulin

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12
Q

sulfonylurea adverse effects

A
  • Mild GI upset – nausea, vomiting, diarrhoea

- Hypoglycaemia (works at low [glucose])

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13
Q

sulfonylurea contradictions

A
  • Renal and hepatic disease

- Caution for people at risk of hypoglycaemia

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14
Q

sulfonylurea drug interactions

A
  • Other hypoglycaemic agents

- Loop and thiazide like diuretics ↑glucose so can reduce SU action

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15
Q

name 2 thiazolidinedione (glitazones)

A

Pioglitazone, rosiglitazone

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16
Q

Glitazone MoA

A

Insulin sensitisation in muscle and adipose, ↓hepatic glucose output by activation of PPAR-γ

t1/2 not related to duration of action – 6-8 weeks for benefit; used much less frequently than other agents

Weight gain because of fat cell differentiation

17
Q

glitazone adverse effects

A
  • GI upset, fluid retention
  • Fracture risk
  • Bladder cancer
18
Q

glitazone contradictions

A

Heart failure due to fluid retention

19
Q

glitazone drug interactions

A

other hypoglycaemic drugs

20
Q

name 2 SGLT-2 inhibitors (gliflozins)

A

Dapagliflozin, canagliflozin

21
Q

gliflozin MoA

A

↓↓glucose absorption from tubular filtrate, ↑urinary glucose excretion

Competitive reversible inhibition of SGLT-2 in PCT

Modest weight loss, hypoglycaemic risk is low; used in TIIDM as add on therapy

22
Q

gliflozin adverse effects

A
  • UTI and genital infections

- Thirst and polyuria

23
Q

gliflozin contradictions

A

Hypovolaemia - possibly hypotension

24
Q

gliflozin drug interactions

A
  • Antihypertensive

- other hypoglycaemic agents

25
Q

name 2 DPP-4 inhibitors (gliptins)

A

Sitagliptin, saxagliptin

26
Q

gliptin MoA

A

Prevent incretin degradation - ↑[incretin] levels

Glucose dependant so postprandial action; doesn’t stimulate insulin secretion at normal blood glucose – lower hypoglycaemic risk

Supress appetite

27
Q

gliptin adverse effects

A
  • GI upset

- small pancreatitis risk

28
Q

gliptin contradictions

A
  • Avoid in pregnancy

- History of pancreatitis

29
Q

gliptin drug interactions

A
  • other hypoglycaemic agents

- drugs ↑glucose can oppose gliptin action – thiazide like and loop diuretics

30
Q

name 2 GLP-1 receptor agonists (incretin mimics)

A

Exenatide

liraglutide

31
Q

GLP-1 receptor agonists MoA

A

↑glucose dependant synthesis of insulin secretion from β-cells; activate GLP-1 receptor – resistant to degradation by DPP-4

Given by subcutaneous injection; promotes satiety

NICE suggest add-on if triple therapy ineffective

32
Q

GLP-1 receptor agonists adverse effects

A

GI upset, decreased appetite with weight loss

33
Q

GLP-1 receptor agonists contradictions

A

Renal impairment

34
Q

GLP-1 receptor agonists drug interactions

A

other hypoglycaemic agents