COUGH
Introduction:
a protective reflex meant for expulsion of respiratory secretions or
foreign particles from air passages
due to stimulation of:
• mechano- or chemoreceptors in throat/ respiratory passages or
• stretch receptors in the lungs
Two types:
• Useless cough(non productive)
• Useful cough(productive)
Classification of drugs:
1. Pharyngeal demulcents:
Lozenges, cough drops, linctuses containing syrup, glycerine, liquorice.
2. Expectorants (Mucokinetics):
(a) Bronchial secretion enhancers:
Sodium or Potassium citrate, Potassium iodide, Guaiphenesin
(Glyceryl guaiacolate), balsum of Tolu, Vasaka, Ammonium chloride.
(b) Mucolytics:
Bromhexine, Ambroxol, Acetyl cysteine, Carbocisteine
3. Antitussives (Cough centre suppressants):
(a) Opioids:
Codeine, Ethylmorphine, Pholcodeine.
(b) Nonopioids:
Noscapine, Dextromethorphan, Chlophedianol.
(c) Antihistamines:
Chlorpheniramine, Diphenhydramine, Promethazine.
(d) Peripherally acting:
Prenoxdiazine.
4. Adjuvant antitussives:
Bronchodilators: Salbutamol, Terbutalin.
DEMULCENTS AND EXPECTORANTS:
Demulcents: Sooth the throat and reduce afferent impulses from
pharyngeal mucosa
Expectorants (Mucokinetics) : increase bronchial secretion or reduce
its viscosity
 Sodium and potassium citrate: increase bronchial secretion by salt
action
 Potassium iodide: irritate the airway mucosa(can affect thyroid
function)
 Guaiphenesin, vasaka, tolu balsum:
 Plant products
 Enhance bronchial secretion
 Increase mucociliary function
 Ammonium salts: reflexly increase respiratory secretions
US-FDA has stopped marketing of all expectorants, except
guaiphenesin
Steam inhalation and proper hydration may be more helpful in
clearing airway mucus
MUCOLYTICS:
Bromhexine:
derivative of Adhatoda vasica (Vasaka)
depolymerises mucopolysaccharides directly as well as by liberating
lysosomal enzymes
useful if mucus plugs are present
Side effects:
rhinorrhoea and lacrimation, nausea, gastric irritation, hypersensitivity
Ambroxol:
metabolite of bromhexine
Acetylcysteine:
opens disulfide bonds in mucoproteins present in sputum
has to be administered directly into the respiratory tract
Carbocisteine:
MOA similar to acetylcysteine
Administered orally(250–750 mg TDS)
may break gastric mucosal barrier : contraindicated in peptic ulcer
patients
ANTITUSSIVES:
MOA:
• act in the CNS to raise the threshold of cough centre or
• act peripherally in the respiratory tract to reduce tussal impulses
• or both
Used in:
• dry nonproductive cough
• cough is unduly tiring, disturbs sleep or
• Is hazardous(hernia, piles, cardiac disease, ocular surgery)
Opioids:
Codeine:
Qualitatively similar to and less potent than morphine
more selective for cough centre
Suppresses cough for about 6 hours(standard antitussive)
Antagonised by naloxone
Abuse liability is low(still present)
Side effect:
Constipation(m/c), respiratory depression and drowsiness
Ethylmorphine:
similar & less constipating than codein
Pholcodeine:
no analgesic or addicting property
similar in efficacy to codeine
Longer acting
NONOPIOIDS:
Noscapine (Narcotine):
An opium alkaloid of the benzoisoquinoline series
no narcotic, analgesic or dependence inducing properties
nearly equipotent to codeine
useful in spasmodic cough
can release histamine and produce bronchoconstriction in asthmatics
Side effects:
Headache and nausea
Dextromethorphan:
synthetic central NMDA (N-methyl D-aspartate) receptor antagonist
d-isomer is antitussive while l-isomer is analgesic
does not depress mucociliary function
devoid of constipating action
Antitussive action: equivalent to codein
Side effect:
 Dizziness, nausea, drowsiness.
 hallucinations and ataxia at high doses
ANTIHISTAMINES:
Used for sedative and anticholinergic action
Not selective for cough centre
May reduce secreations
Useful for cough in respiratory allergic states
Commonly used drugs:
 Chlorpheniramine (2–5 mg),
 Diphenhydramine(15–25 mg)
 Promethazine (15–25 mg
PERIPHERALLY ACTING ANTITUSSIVES:
Prenoxdiazine:
desensitizes the pulmonary stretch receptors and reduces tussal
impulses originating in the lungs
indicated in cough of bronchial origin
Efficacy is not good enough
BRONCHODILATORS:
Bronchospasm can induce or aggravate cough
Pulmonary receptors stimulation(in bronchial hyperactivity) can
trigger both
Cough &
Bronchoconstriction
Bronchodilators improve the velocity of airflow during coughing

Cough

  • 1.
  • 2.
    Introduction: a protective reflexmeant for expulsion of respiratory secretions or foreign particles from air passages due to stimulation of: • mechano- or chemoreceptors in throat/ respiratory passages or • stretch receptors in the lungs Two types: • Useless cough(non productive) • Useful cough(productive)
  • 3.
    Classification of drugs: 1.Pharyngeal demulcents: Lozenges, cough drops, linctuses containing syrup, glycerine, liquorice. 2. Expectorants (Mucokinetics): (a) Bronchial secretion enhancers: Sodium or Potassium citrate, Potassium iodide, Guaiphenesin (Glyceryl guaiacolate), balsum of Tolu, Vasaka, Ammonium chloride. (b) Mucolytics: Bromhexine, Ambroxol, Acetyl cysteine, Carbocisteine
  • 4.
    3. Antitussives (Coughcentre suppressants): (a) Opioids: Codeine, Ethylmorphine, Pholcodeine. (b) Nonopioids: Noscapine, Dextromethorphan, Chlophedianol. (c) Antihistamines: Chlorpheniramine, Diphenhydramine, Promethazine. (d) Peripherally acting: Prenoxdiazine. 4. Adjuvant antitussives: Bronchodilators: Salbutamol, Terbutalin.
  • 5.
    DEMULCENTS AND EXPECTORANTS: Demulcents:Sooth the throat and reduce afferent impulses from pharyngeal mucosa Expectorants (Mucokinetics) : increase bronchial secretion or reduce its viscosity  Sodium and potassium citrate: increase bronchial secretion by salt action  Potassium iodide: irritate the airway mucosa(can affect thyroid function)
  • 6.
     Guaiphenesin, vasaka,tolu balsum:  Plant products  Enhance bronchial secretion  Increase mucociliary function  Ammonium salts: reflexly increase respiratory secretions US-FDA has stopped marketing of all expectorants, except guaiphenesin Steam inhalation and proper hydration may be more helpful in clearing airway mucus
  • 7.
    MUCOLYTICS: Bromhexine: derivative of Adhatodavasica (Vasaka) depolymerises mucopolysaccharides directly as well as by liberating lysosomal enzymes useful if mucus plugs are present Side effects: rhinorrhoea and lacrimation, nausea, gastric irritation, hypersensitivity
  • 8.
    Ambroxol: metabolite of bromhexine Acetylcysteine: opensdisulfide bonds in mucoproteins present in sputum has to be administered directly into the respiratory tract Carbocisteine: MOA similar to acetylcysteine Administered orally(250–750 mg TDS) may break gastric mucosal barrier : contraindicated in peptic ulcer patients
  • 9.
    ANTITUSSIVES: MOA: • act inthe CNS to raise the threshold of cough centre or • act peripherally in the respiratory tract to reduce tussal impulses • or both Used in: • dry nonproductive cough • cough is unduly tiring, disturbs sleep or • Is hazardous(hernia, piles, cardiac disease, ocular surgery)
  • 10.
    Opioids: Codeine: Qualitatively similar toand less potent than morphine more selective for cough centre Suppresses cough for about 6 hours(standard antitussive) Antagonised by naloxone Abuse liability is low(still present) Side effect: Constipation(m/c), respiratory depression and drowsiness
  • 11.
    Ethylmorphine: similar & lessconstipating than codein Pholcodeine: no analgesic or addicting property similar in efficacy to codeine Longer acting
  • 12.
    NONOPIOIDS: Noscapine (Narcotine): An opiumalkaloid of the benzoisoquinoline series no narcotic, analgesic or dependence inducing properties nearly equipotent to codeine useful in spasmodic cough can release histamine and produce bronchoconstriction in asthmatics Side effects: Headache and nausea
  • 13.
    Dextromethorphan: synthetic central NMDA(N-methyl D-aspartate) receptor antagonist d-isomer is antitussive while l-isomer is analgesic does not depress mucociliary function devoid of constipating action Antitussive action: equivalent to codein Side effect:  Dizziness, nausea, drowsiness.  hallucinations and ataxia at high doses
  • 14.
    ANTIHISTAMINES: Used for sedativeand anticholinergic action Not selective for cough centre May reduce secreations Useful for cough in respiratory allergic states Commonly used drugs:  Chlorpheniramine (2–5 mg),  Diphenhydramine(15–25 mg)  Promethazine (15–25 mg
  • 15.
    PERIPHERALLY ACTING ANTITUSSIVES: Prenoxdiazine: desensitizesthe pulmonary stretch receptors and reduces tussal impulses originating in the lungs indicated in cough of bronchial origin Efficacy is not good enough
  • 16.
    BRONCHODILATORS: Bronchospasm can induceor aggravate cough Pulmonary receptors stimulation(in bronchial hyperactivity) can trigger both Cough & Bronchoconstriction Bronchodilators improve the velocity of airflow during coughing