TOpic 15, selective b2 stimulants and other bronchodialators Flashcards
1
Q
goals of therapy
A
- reduce intensity and frequency of symptoms. 2. Relief of acute asthma symptoms. 3. Long term therapy: prevention of inflammation
2
Q
how to treat asthmatic patients
A
- Asses the severity of asthma and start the treatment according to the guidelines 2. increase Intensity of treatment stepwise, until the asthma is well controlled 3. reduce dose of anti-inflammatory agents gradually (if possible), to minimize the side effects
3
Q
drugs used in asthma treatment
A
are:
4
Q
Short-acting b__2 agonists (SABA):
- Rapid onset (5-30min)
- Duration: 4-6 hours
- Symptomatic treatment of acute bronchospasm – inhaler
- Used as relievers
- b2 agonists aren’t anti-inflammatory so never use alone
- Although it may be used as a monotherapy for patients with intermittent asthma or exercise-induced asthma
Action:
- Bronchodilation
- mucociliary transport
- ¯ release of inflammatory mediators
Adverse effects:
- Cardiovascular disturbances (Tachycardia, palpitation, angina)
- Direct cardiac effect (b1, b2)
- Vasodilation (b2)
- Presnaptic norepinephrine release (b2)
- Hypokalemia
- Metabolic effects: Hyperglycemia, hyperlipidemia
- Hypomagnesemia
- Skeletal muscle tremors
- ¯ PaO2
- Mild loss of appetite, disturbed sleep
- Development of tolerance
Drugs:
- Albuterol (salbutamol)
- Levalbuterol
- Terbutaline
- Fenoterol
A
Short-acting b__2 agonists (SABA):
- Rapid onset (5-30min)
- Duration: 4-6 hours
- Symptomatic treatment of acute bronchospasm – inhaler
- Used as relievers
- b2 agonists aren’t anti-inflammatory so never use alone
- Although it may be used as a monotherapy for patients with intermittent asthma or exercise-induced asthma
Action:
- Bronchodilation
- mucociliary transport
- ¯ release of inflammatory mediators
Adverse effects:
- Cardiovascular disturbances (Tachycardia, palpitation, angina)
- Direct cardiac effect (b1, b2)
- Vasodilation (b2)
- Presnaptic norepinephrine release (b2)
- Hypokalemia
- Metabolic effects: Hyperglycemia, hyperlipidemia
- Hypomagnesemia
- Skeletal muscle tremors
- ¯ PaO2
- Mild loss of appetite, disturbed sleep
- Development of tolerance
Drugs:
- Albuterol (salbutamol)
- Levalbuterol
- Terbutaline
- Fenoterol
5
Q
what are the LABA drugs
A
Albuterol (salbutamol)
Levalbuterol
Terbutaline
Fenoterol
6
Q
Long-acting b__2 agonists (LABA):
A
Long-acting b__2 agonists (LABA):
- Slower onset of action
- Duration: 12 hours
- Higher lipophilicity è accumulation in membranes
- Not used for quick relief of an acute asthma attack, but rather as controllers in patients with moderat/severe asthma and COPD
- Never used as a monotherapy.
- Only used in a combination with asthma controlling-medication
- Inhaled corticosteroids (main choice)
- Synergistic effect: Small dose of steroid + LABA is stronger than a high dose of steroid
- Only used in a combination with asthma controlling-medication
Action:
- Bronchodilation
Adverse effects:
- Same as SABA
Drugs:
-
Salmeterol (=albuterol)
- Partial agonist
-
Formoterol
- Faster onset of action
-
Clenbuterol
- Oral agent
-
Bambuterol (® Terbutaline)
- Oral agent
-
Indacaterol, olodaterol, vilanterol
- Duration > 24h (VLABA)
7
Q
what are the LABA drugs
A
Drugs:
-
Salmeterol (=albuterol)
- Partial agonist
-
Formoterol
- Faster onset of action
-
Clenbuterol
- Oral agent
-
Bambuterol (® Terbutaline)
- Oral agent
-
Indacaterol, olodaterol, vilanterol
- Duration > 24h (VLABA)
8
Q
Theophylline (xanthine)
A
Other bronchodilators:
Xanthines:
- Other xanthines with no bronchodilator effect: caffeine, theobromine
-
Theophylline:
- It gives rise to aminophylline
-
Therapeutic effect:
-
Bronchodilation
- decrease a1 receptor
- decrease PDE3 [phosphodiesterase] è cAMP
- decrease Release of inflammatory mediators
- ¯decrease PDE4
- decrease a1 receptor
- HDAC2
- increase Ciliary activity
-
Bronchodilation
-
Side effects:
- CNS
- Anxiety
- Insomnia
- Tremor
- Seizures
- Cardiovascular:
- At low doses, mild elevation of BP (a receptor decrease)
- At higher doses, “inodilator” effect ( cAMP)
- Diuretic effect
- increase GFR
- decrease Tubular sodium resorption
- Gastrointestinal secretions increase
- Gastric acid
- Digestive enzyme
- CNS
-
Pharmacokinetics:
- Good oral absorption
- Narrow therapeutic index
-
Clinical use:
- Prevention of asthmatic attack (oral, extended-release tablets)
- Reliever in acute asthma (aminophylline IV)
9
Q
MaChR antagonists?
A
mAChR antagonists:
-
Mechanism of action:
- M3 is present in bronchial smooth muscle cells (they normally cause contraction)
- We use only drugs having a quaternary nitrogen nowadays because:
- Plasma concentration stays low
- The drugs don’t enter CNS
-
Therapeutic effects:
- Bronchodilation
- decrease Bronchial secretions
- Block vagally-mediated contraction of airway smooth muscle and mucus secretion
-
Clinical use:
- Relievers (ipratropium) or controllers in asthma and COPD
- Used adjacent to b2 agonists
- Instead of b2 agonists, if those are contraindicated or not tolerated
- If cholinergic tone is elevated (e.g. nocturnal asthma)
- Patients with concomitant COPD
- Asthmatic attack – alternative or add-on drugs for SABA
- Adverse effects:
- Dry mouth
- Cough
- Relievers (ipratropium) or controllers in asthma and COPD
-
Drugs:
- Atropine
-
Ipratropium
- Non-selective muscarinic receptor antagonist
- Onset: < 15min
- Duration: 4-6h
- Administration: 3x/day
-
Tiotropium, glycopyrronium, aclidinium, umeclidinium
- Selective for M3 receptors (slower dissociation)
- Longer effect: T1/2 = 11h - 6 days (except aclidinium)
- Administration: 1x/day
10
Q
A