Asthma Flashcards

1
Q

What is the primary mechanism of action of salbutamol?

A

Agonist at the β2 receptor on airway smooth muscle cells. Activation reduces Ca2+ entry and this prevents smooth muscle contraction.

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2
Q

What does salbutamol act on?

A

Beta 2 (β2) adrenergic receptor

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3
Q

What are the side effects of salbutamol?

A

Palpitations/ agitation
Tachycardia/ Arrythmias
Hypokalaemia (at higher doses)

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4
Q

Why can cardiac side effects of salbutamol be seen?

A

Beta 2 selectivity is not absolute – as a result, cardiac (beta 1) effects can be seen.

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5
Q

What can exacerbate the hypokalaemia seen with patients given salbutamol?

A

Hypokalaemia can be caused via an effect on sodium/ potassium ATPase. This effect can be exacerbated by coadministration with corticosteroids

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6
Q

What is the mechanism of action of Fluticasone?

A

Fluticasone directly decreases inflammatory cells such as eosinophils, monocytes, mast cells, macrophages, and dendritic cells. It reduces the number of these cells and also the number of cytokines they produce

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7
Q

What is the drug target of Fluticasone?

A

Glucocorticoid receptor

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8
Q

What are the local side effects of Fluticasone?

A

Sore throat, hoarse voice, opportunistic oral infections

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9
Q

What is the relevance of Fluticasone having a low bioavailability?

A

Oral bioavailability <1%. Therefore, any systemic delivery via the inhaled route is predominantly through the pulmonary vasculature.

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10
Q

What is the mechanism of action of Mometasone?

A

directly decreases inflammatory cells such as eosinophils, monocytes, mast cells, macrophages, and dendritic cells. It reduces the number of these cells and also the number of cytokines they produce.

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10
Q

What is mometasone similar to?

A

Fluticasone and Budesonide

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11
Q

Which is the least potent between Mometasone, Fluticasone and Budesonide?

A

Budensonide

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12
Q

What is the bioavailability of Budesonide and what are the implications of this?

A

Oral bioavailability >10%. Therefore, inhaled budesonide will still result in some systemic absorption through the gastro-intestinal tract.

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13
Q

What is the mechanism of action of Montelukast?

A

Antagonism of CysLT1 leukotriene receptor on eosinophils, mast cells and airway smooth muscle cells decreases eosinophil migration, broncho-constriction and inflammation induced oedema

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14
Q

What is the drug target of montelukast?

A

CysLT1 leukotriene receptor

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15
Q

What are the side effects of montelukast?

A

Mild side effects:
Diarrhoea
Fever
Headaches
Nausea or vomiting

Serious side effects:
Mood changes
Anaphylaxis

16
Q

How long should you wait before doing exercise when giving Montelukast as prophylaxis of exercise-induced bronchoconstriction?

A

wait 2 hours before initiating exercise.

17
Q

Why is salbutamol inhalation preferred over oral?

A

Faster action

Reduced systemic side effects

Easier

Inhaled dose 10x smaller than oral dose

LOCAL VS SYSTEMIC

18
Q

Only 20% of the inhaled salbutamol gets to the lungs - where does the rest go?

A
  1. EXHALED
  2. ABSORPTION FROM LUNGS
  3. MUCOCILIARY CLEARANCE
  4. ORAL SWALLOWED
  5. ABSORBED THROUGH MUCOUS MEMBRANE IN ORAL CAVITY AND PHARYNX
19
Q

What is the mechanism of action for montelukast and why might it be particularly useful for NSAID (Non-steroidal anti-inflammatory drug)-induced asthma?

A

When medications such as NSAIDs or aspirin block the COX-1 enzyme, production of thromboxane and some anti-inflammatory prostaglandins is decreased, and in patients with aspirin-induced asthma, this results in theoverproduction ofpro-inflammatory leukotrienes, which can cause severe exacerbations of asthma

Montelukast works by inhibiting the leukotriene receptor