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Respiratory Drugs
Respiratory Drugs
 The respiratory agents presented here are divided into two primary categories.
 The first group includes drugs that treat acute and relatively minor problems, such as
 nasal congestion,
 coughing,
 and seasonal allergies.
 The second category includes drugs that treat more chronic and serious airway obstructions,
such as
 bronchial asthma,
 chronic bronchitis,
 and emphysema
Antitussives
 Antitussive drugs are used to suppress coughing associated with the common cold and other
minor throat irritations.
 Antitussives are usually recommended for short-term use in relieving symptomatic coughing
 Coughing is a type of defense mechanism that can help expel mucus and foreign material from
the upper respiratory tract
 Antitussives may be helpful in treating an annoying dry cough, but use of these drugs to treat an
active and productive cough may not be justified
Antitussives
 codeine and similar opiate derivatives suppress the cough reflex by a central inhibitory effect
 Other nonopioid antitussives work by inhibiting the irritant effects of histamine on the respiratory
mucosa or by a local anesthetic action on the respiratory epithelium.
Antitussives
Adverse effects
The primary adverse effect associated with most antitussives is sedation. Dizziness and
gastrointestinal upset may also occur.
Decongestants
 Congestion within and mucous discharge from the upper respiratory tract are familiar symptoms
of many conditions.
 Allergies, the common cold, and various respiratory infections often produce a runny nose and a
stuffy head sensation
 Decongestants used to treat these symptoms are usually alpha-1–adrenergic agonists
 MOA: These agents bind to alpha-1 receptors located on the blood vessels of the nasal mucosa
and stimulate vasoconstriction, thus effectively drying up the mucosal vasculature and
decreasing local congestion in the nasal passages
Decongestants
 Depending on the preparation, these agents may be taken systemically or applied locally to the
nasal mucosa via aerosol sprays
Adverse effects
 The primary adverse effects associated with decongestants are headache, dizziness,
nervousness, nausea, and cardiovascular irregularities (increased blood pressure, palpitations).
Antihistamines
Histamine is an endogenous chemical that is involved in the normal regulation of certain
physiologic functions (gastric secretion, CNS neural modulation), as well as various
hypersensitivity (allergic reactions).
Histamine exerts its effects on various cells through four primary receptor subtypes:
 H1,
 H2,
 H3,
 and H4 receptors
Antihistamines
H1-receptor blockers
Antihistamines are drugs that specifically block the H1 subtype of histamine receptors; that is, the
effects of histamine during allergic reactions, respiratory infections, and so forth are mediated
primarily through the H1 receptor located on vascular, respiratory, and other tissues.
H2-receptor blockers
H2 receptors are involved primarily in the regulation of gastric acid secretion. Drugs that
selectively block the H2 receptor (referred to simply as H2 antagonists) may help control gastric
secretion in conditions such as peptic ulcer;
Antihistamines
H3-receptor blockers
A third receptor subtype, the H3 receptor, has been identified, and this subtype may be involved in
the local regulation of histamine release from CNS nerve terminals
H4-receptors
► a new H4 receptor has been identified on blood cells or cells derived from blood cells.
► The clinical and pharmacologic significance of H3 and H4 receptors remains to be determined.
Antihistamines
Therapeutic indications of Antihistamines
 By blocking the effects of histamine on the upper respiratory tissues, these drugs help
decrease;
 Nasal congestion, mucosal irritation and discharge (rhinitis, sinusitis), and conjunctivitis that are
caused by inhaled allergens.
 Similarly, antihistamines may decrease the coughing and sneezing associated with the common
cold.
 Antihistamines may be used as an adjunct in patients with asthma to help control rhinitis and
sinusitis
Antihistamines
Adverse effects
 The primary adverse effects associated with antihistamines are sedation, fatigue, dizziness,
blurred vision, and incoordination.
 Gastrointestinal distress (nausea, vomiting) is also quite common. Certain side effects, however,
are related directly to each drug’s ability to cross the blood-brain barrier
First-generation antihistamines
 The original or “first-generation” antihistamines readily cross the blood-brain barrier and enter
the brain, thus causing CNS-related side effects such as sedation and psychomotor slowing
Second-generation antihistamines
 Do not easily cross the blood brain barrier, and the risk of sedation and other CNS side
effects is reduced
Antihistamines
 Newer “second-generation” antihistamines, also known as nonsedating antihistamines, include
cetirizine, loratadine, desloratidine and fexofenadine
Mucolytics and Expectorants
 Mucolytic drugs attempt to decrease the viscosity of respiratory secretions
 Expectorant drugs facilitate the production and ejection of mucus.
 These drugs are used to prevent the accumulation of thick, viscous secretions that can clog
respiratory passages and lead to pulmonary problems.
Acetylcysteine
 The primary mucolytic drug currently in use is acetylcysteine.
 This drug is thought to work by splitting the disulfide bonds of respiratory mucoproteins, thus
forming a less viscous secretion.
 Acetylcysteine is usually administered directly to the respiratory mucosa by inhalation or
intratracheal instillation (through a tracheostomy)
Adverse effects
 The primary adverse effects associated with this drug include nausea, vomiting, inflammation
of the oral mucosa (stomatitis), and rhinorrhea. However, serious adverse effects are relatively
rare.
Guaifenesin
 Several expectorant agents have been used in the past, but guaifenesin is the only drug
currently acknowledged by the FDA to have evidence of therapeutic effects
 This drug is administered to increase the production of respiratory secretions, thus
encouraging ejection of phlegm and sputum
Adverse effects
 The primary adverse effect associated with guaifenesin is gastrointestinal upset, which is
exacerbated if excessive doses are taken or if this drug is taken on an empty stomach.
Chronic Obstructive
Pulmonary Disease
Chronic obstructive pulmonary disease, or COPD,
refers to a group of diseases that cause airflow
blockage and breathing-related problems
Chronic bronchitis
Chronic bronchitis irritates your bronchial tubes,
which carry air to and from your lungs. In response,
the tubes swell and mucus (phlegm) builds
up along the lining. The buildup narrows the tube’s
opening, making it hard to get air into and out of your
lungs
Chronic Obstructive
Pulmonary Disease
Emphysema
Emphysema is the breakdown of the walls of the tiny air sacs (alveoli) at the end of the bronchial
tubes, in the “bottom” of your lung.
Drugs used are;
Bronchodilators (beta-adrenergic agonists)
xanthine derivatives,
Anticholinergics
and anti-inflammatory agents (glucocorticoids,others)
Beta-Adrenergic Agonists
 Respiratory smooth-muscle cells contain the beta-2 subtype of adrenergic receptors.
 Stimulation of these beta-2 receptors results in relaxation of bronchiole smooth muscle.
 Hence, drugs that stimulate these beta-2 adrenergic receptors (i.e., betaadrenergic agonists) produce
bronchodilation and can be used to prevent or inhibit airway obstruction in bronchospastic diseases
 Beta-adrenergic drugs can be administered orally, subcutaneously, or by inhalation.
 Another method of inhaling beta agonists is through a nebulizer. These devices mix the drug with air to form a
fine mist that is inhaled through a mask, thus reaching the lungs over a more prolonged period (10 minutes).
Beta-Adrenergic Agonists
Adverse Side Effects
 Prolonged use of beta-2 drugs may also cause tolerance; the dose must be increased to achieve
therapeutic effects when this occurs
 With prolonged or excessive use, inhaled adrenergic agonists may actually increase bronchial
responses to allergens and other irritants
 Adrenergic agonists that also stimulate beta-1 receptors may cause cardiac irregularities if they
reach the myocardium through the systemic circulation.
 Similarly, stimulation of CNS adrenergic receptors may produce symptoms of nervousness,
restlessness, and tremor.
Xanthine Derivatives
 These drugs may enhance bronchodilation by inhibiting the phosphodiesterase (PDE)
enzyme located in bronchial smooth-muscle cells.
 PDE breaks down cAMP; inhibiting this enzyme results in higher intracellular cAMP
concentrations.
 cAMP is the second messenger that brings about respiratory smooth-muscle relaxation and
subsequent bronchodilation.
 By inhibiting PDE, theophylline can prolong the effects of this second messenger and
increase bronchodilation.
Xanthine Derivatives
Theophylline may likewise help produce bronchodilation by other mechanisms, such as inhibition of intracellular calcium
release and stimulation of catecholamine release.
Adverse Side Effects
 nausea,
 confusion,
 irritability, and restlessness
 ardiac arrhythmias
 seizures
To prevent toxicity, the dosage should be individualized for each patient, using the lowest possible dose
Anticholinergic Drugs
 The lungs receive extensive parasympathetic innervation via the vagus nerve.
 The efferent fibers of the vagus nerve release acetylcholine onto respiratory smooth-muscle
cells, which contain muscarinic cholinergic receptors.
 When stimulated, these receptors mediate bronchoconstriction.
 Consequently, drugs that block muscarinic cholinergic receptors prevent acetylcholine-
induced bronchoconstriction, thus improving airflow in certain types of bronchospastic
disease.
Anticholinergic Drugs
Adverse Side Effects
 Systemic side effects associated with atropine include dry mouth, constipation, urinary
retention, tachycardia, blurred vision, and confusion
Glucocorticoids
Glucocorticoids (also known as corticosteroids) inhibit the inflammatory response in several
important ways.
These drugs directly affect the genes and transcription factors that produce inflammatory
components.
As a result, the drugs inhibit the production of proinflammatory products (cytokines
prostaglandins, leukotrienes, and so forth) while increasing the production of anti-inflammatory
proteins.
Glucocorticoids also reverse the increase in vascular permeability and inhibit the migration of
neutrophils and monocytes typically occurring during the inflammatory response
Glucocorticoids
Adverse Side Effects
 osteoporosis,
 skin breakdown,
 and muscle wasting
 retardation of growth in children,
 glaucoma,
 hyperglycemia,
 aggravation of diabetes mellitus, and hypertension
Thank You

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Respiratory Drugs final.pptx

  • 2. Respiratory Drugs  The respiratory agents presented here are divided into two primary categories.  The first group includes drugs that treat acute and relatively minor problems, such as  nasal congestion,  coughing,  and seasonal allergies.  The second category includes drugs that treat more chronic and serious airway obstructions, such as  bronchial asthma,  chronic bronchitis,  and emphysema
  • 3. Antitussives  Antitussive drugs are used to suppress coughing associated with the common cold and other minor throat irritations.  Antitussives are usually recommended for short-term use in relieving symptomatic coughing  Coughing is a type of defense mechanism that can help expel mucus and foreign material from the upper respiratory tract  Antitussives may be helpful in treating an annoying dry cough, but use of these drugs to treat an active and productive cough may not be justified
  • 4. Antitussives  codeine and similar opiate derivatives suppress the cough reflex by a central inhibitory effect  Other nonopioid antitussives work by inhibiting the irritant effects of histamine on the respiratory mucosa or by a local anesthetic action on the respiratory epithelium.
  • 5. Antitussives Adverse effects The primary adverse effect associated with most antitussives is sedation. Dizziness and gastrointestinal upset may also occur.
  • 6. Decongestants  Congestion within and mucous discharge from the upper respiratory tract are familiar symptoms of many conditions.  Allergies, the common cold, and various respiratory infections often produce a runny nose and a stuffy head sensation  Decongestants used to treat these symptoms are usually alpha-1–adrenergic agonists  MOA: These agents bind to alpha-1 receptors located on the blood vessels of the nasal mucosa and stimulate vasoconstriction, thus effectively drying up the mucosal vasculature and decreasing local congestion in the nasal passages
  • 7. Decongestants  Depending on the preparation, these agents may be taken systemically or applied locally to the nasal mucosa via aerosol sprays Adverse effects  The primary adverse effects associated with decongestants are headache, dizziness, nervousness, nausea, and cardiovascular irregularities (increased blood pressure, palpitations).
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  • 9. Antihistamines Histamine is an endogenous chemical that is involved in the normal regulation of certain physiologic functions (gastric secretion, CNS neural modulation), as well as various hypersensitivity (allergic reactions). Histamine exerts its effects on various cells through four primary receptor subtypes:  H1,  H2,  H3,  and H4 receptors
  • 10. Antihistamines H1-receptor blockers Antihistamines are drugs that specifically block the H1 subtype of histamine receptors; that is, the effects of histamine during allergic reactions, respiratory infections, and so forth are mediated primarily through the H1 receptor located on vascular, respiratory, and other tissues. H2-receptor blockers H2 receptors are involved primarily in the regulation of gastric acid secretion. Drugs that selectively block the H2 receptor (referred to simply as H2 antagonists) may help control gastric secretion in conditions such as peptic ulcer;
  • 11. Antihistamines H3-receptor blockers A third receptor subtype, the H3 receptor, has been identified, and this subtype may be involved in the local regulation of histamine release from CNS nerve terminals H4-receptors ► a new H4 receptor has been identified on blood cells or cells derived from blood cells. ► The clinical and pharmacologic significance of H3 and H4 receptors remains to be determined.
  • 12. Antihistamines Therapeutic indications of Antihistamines  By blocking the effects of histamine on the upper respiratory tissues, these drugs help decrease;  Nasal congestion, mucosal irritation and discharge (rhinitis, sinusitis), and conjunctivitis that are caused by inhaled allergens.  Similarly, antihistamines may decrease the coughing and sneezing associated with the common cold.  Antihistamines may be used as an adjunct in patients with asthma to help control rhinitis and sinusitis
  • 13. Antihistamines Adverse effects  The primary adverse effects associated with antihistamines are sedation, fatigue, dizziness, blurred vision, and incoordination.  Gastrointestinal distress (nausea, vomiting) is also quite common. Certain side effects, however, are related directly to each drug’s ability to cross the blood-brain barrier First-generation antihistamines  The original or “first-generation” antihistamines readily cross the blood-brain barrier and enter the brain, thus causing CNS-related side effects such as sedation and psychomotor slowing Second-generation antihistamines  Do not easily cross the blood brain barrier, and the risk of sedation and other CNS side effects is reduced
  • 14. Antihistamines  Newer “second-generation” antihistamines, also known as nonsedating antihistamines, include cetirizine, loratadine, desloratidine and fexofenadine
  • 15. Mucolytics and Expectorants  Mucolytic drugs attempt to decrease the viscosity of respiratory secretions  Expectorant drugs facilitate the production and ejection of mucus.  These drugs are used to prevent the accumulation of thick, viscous secretions that can clog respiratory passages and lead to pulmonary problems.
  • 16. Acetylcysteine  The primary mucolytic drug currently in use is acetylcysteine.  This drug is thought to work by splitting the disulfide bonds of respiratory mucoproteins, thus forming a less viscous secretion.  Acetylcysteine is usually administered directly to the respiratory mucosa by inhalation or intratracheal instillation (through a tracheostomy) Adverse effects  The primary adverse effects associated with this drug include nausea, vomiting, inflammation of the oral mucosa (stomatitis), and rhinorrhea. However, serious adverse effects are relatively rare.
  • 17. Guaifenesin  Several expectorant agents have been used in the past, but guaifenesin is the only drug currently acknowledged by the FDA to have evidence of therapeutic effects  This drug is administered to increase the production of respiratory secretions, thus encouraging ejection of phlegm and sputum Adverse effects  The primary adverse effect associated with guaifenesin is gastrointestinal upset, which is exacerbated if excessive doses are taken or if this drug is taken on an empty stomach.
  • 18. Chronic Obstructive Pulmonary Disease Chronic obstructive pulmonary disease, or COPD, refers to a group of diseases that cause airflow blockage and breathing-related problems Chronic bronchitis Chronic bronchitis irritates your bronchial tubes, which carry air to and from your lungs. In response, the tubes swell and mucus (phlegm) builds up along the lining. The buildup narrows the tube’s opening, making it hard to get air into and out of your lungs
  • 19. Chronic Obstructive Pulmonary Disease Emphysema Emphysema is the breakdown of the walls of the tiny air sacs (alveoli) at the end of the bronchial tubes, in the “bottom” of your lung. Drugs used are; Bronchodilators (beta-adrenergic agonists) xanthine derivatives, Anticholinergics and anti-inflammatory agents (glucocorticoids,others)
  • 20. Beta-Adrenergic Agonists  Respiratory smooth-muscle cells contain the beta-2 subtype of adrenergic receptors.  Stimulation of these beta-2 receptors results in relaxation of bronchiole smooth muscle.  Hence, drugs that stimulate these beta-2 adrenergic receptors (i.e., betaadrenergic agonists) produce bronchodilation and can be used to prevent or inhibit airway obstruction in bronchospastic diseases  Beta-adrenergic drugs can be administered orally, subcutaneously, or by inhalation.  Another method of inhaling beta agonists is through a nebulizer. These devices mix the drug with air to form a fine mist that is inhaled through a mask, thus reaching the lungs over a more prolonged period (10 minutes).
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  • 23. Beta-Adrenergic Agonists Adverse Side Effects  Prolonged use of beta-2 drugs may also cause tolerance; the dose must be increased to achieve therapeutic effects when this occurs  With prolonged or excessive use, inhaled adrenergic agonists may actually increase bronchial responses to allergens and other irritants  Adrenergic agonists that also stimulate beta-1 receptors may cause cardiac irregularities if they reach the myocardium through the systemic circulation.  Similarly, stimulation of CNS adrenergic receptors may produce symptoms of nervousness, restlessness, and tremor.
  • 24. Xanthine Derivatives  These drugs may enhance bronchodilation by inhibiting the phosphodiesterase (PDE) enzyme located in bronchial smooth-muscle cells.  PDE breaks down cAMP; inhibiting this enzyme results in higher intracellular cAMP concentrations.  cAMP is the second messenger that brings about respiratory smooth-muscle relaxation and subsequent bronchodilation.  By inhibiting PDE, theophylline can prolong the effects of this second messenger and increase bronchodilation.
  • 25. Xanthine Derivatives Theophylline may likewise help produce bronchodilation by other mechanisms, such as inhibition of intracellular calcium release and stimulation of catecholamine release. Adverse Side Effects  nausea,  confusion,  irritability, and restlessness  ardiac arrhythmias  seizures To prevent toxicity, the dosage should be individualized for each patient, using the lowest possible dose
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  • 27. Anticholinergic Drugs  The lungs receive extensive parasympathetic innervation via the vagus nerve.  The efferent fibers of the vagus nerve release acetylcholine onto respiratory smooth-muscle cells, which contain muscarinic cholinergic receptors.  When stimulated, these receptors mediate bronchoconstriction.  Consequently, drugs that block muscarinic cholinergic receptors prevent acetylcholine- induced bronchoconstriction, thus improving airflow in certain types of bronchospastic disease.
  • 28. Anticholinergic Drugs Adverse Side Effects  Systemic side effects associated with atropine include dry mouth, constipation, urinary retention, tachycardia, blurred vision, and confusion
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  • 30. Glucocorticoids Glucocorticoids (also known as corticosteroids) inhibit the inflammatory response in several important ways. These drugs directly affect the genes and transcription factors that produce inflammatory components. As a result, the drugs inhibit the production of proinflammatory products (cytokines prostaglandins, leukotrienes, and so forth) while increasing the production of anti-inflammatory proteins. Glucocorticoids also reverse the increase in vascular permeability and inhibit the migration of neutrophils and monocytes typically occurring during the inflammatory response
  • 31. Glucocorticoids Adverse Side Effects  osteoporosis,  skin breakdown,  and muscle wasting  retardation of growth in children,  glaucoma,  hyperglycemia,  aggravation of diabetes mellitus, and hypertension
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