Asthma
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Transcript of Asthma
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ASTHMADr.Zulcaif Ahmad
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• It is an episodic, reversible bronchoconstriction to tracheo-bronchial tree due to its hyperactivity towards a variety of stimuli which can be extrinsic or intrinsic.
• Asthma is a reversible condition while bronchoconstriction in COPD is irreversible.
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Early phase of bronchial asthma starts within 5-30mint upon exposure to allergen • APC-CD4 + Helper-T-Cell
Cytokinase B-lymphocyte Memory cell Plasma
cell
IgE
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• Upon Re-entry of antigen : dust particle directly bind to IgE
Degranulation
Bronchoconstirction Histamine (Mast cell Rupture)
Inc.mucous production release
White color sputum
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• Histamine is degraded within 60 minute by HISTAMINASE formed by macrophages.
• Anti histamine has no role in Rx of Bronchial asthma.
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ActivatesHistamine Phospholipase A2
Asachideonic acid metabolism (in cell membrane) Lipoxigenase cyclooxygenase Leukotrine A4 PG-G2 Leukorine B4 Leukotrine C4 D4 E4 PG-H2Chemotactic factor SRSA Tx-A2(platelet
agregate) For monocyte bronchoconstrictionPG-I2(inhb
agregation) lymphocyte inc. Bronchial glandother PG-
D2, E2, secreation F2 vasoconstrictionPain fever
HCL.scr
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C/F (YOUNG <35 yrs)• Episodic symptoms• Chest tightness• Dyspneae (due to bronchoconstriction of mucus
plug)• White sputum with cough• Wheze• 70% of hv Allergic Rhinitis• Sneezing• Post nasal drip• Rhinorrhea
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Classification:
Asthma
Bronchodilators
Methylxanthine Drugs
Antimuscarinic Agents
Corticosteroid
Cromolyn & Nedocromil
Leukotriene pathway inhibtors
Other Drugs
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Approach to Treatment:-• Prevention of the exposure to
antigen• Reduction of bronchial
inflammation and hyperactivity• Dilatation of the narrowed bronchi.
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Sympathomimetic Drugs/
Bronchodilators
Non-Selective
Epinephrine, Ephedrine,
Isoproternol
Beta selcetive
Beta 2 selective
Salbutamol, Terbutaline, Femoterol
Salbutamol, Terbutaline, Femoterol
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Bronchodilators
• Sympathomimetics (β2 receptor agonist), Xanthine derivatives, Anti-cholinergics / muscarinics.
• Sympathomimetic drugs• adrenalin is an agonist for the α1,
α2, β1, β2 receptors. Binding with the β2 receptor it causes bronchodilatation but binding on the β1 receptors it causes ↑ HR, ↑ BP, ↑ O2 demand.
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• Non-selective• Epinephrine, Ephedrine,
Isoproterenol {ephedrine causes tachyphylaxis / acute tolerance}
• β receptor selective drugs• Isopropanolol, Isoprenalin• β2 receptor selective• Salbutamol, Terbutaline, Femoterol• β receptors are also present in the
peripheral vasculature, so long term use may cause hypotension.
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Long-acting beta-agonists:• Long-acting beta-agonists(LABAs)
dilate the airway for up to 12 hours and are to be taken along with your inhaled steroids. Currently, researchers do not think that long-acting bronchodilators can reduce inflammation on their own, but they may help the inhaled steroids to work better.
• Examples:• Formoterol• Salmeterol
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The selective β2 agonists• They can be given orally or
inhalation• They act selectively on β2
receptors• They have long duration of action• Bronchodilatation is maximal in 30
min when given by inhalation and persists for 2-3 hours
• They produce less cardio-vascular side effects
• Orally they are given in doses of 4mg 3-4 times
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Mechanism of Action—it acts in the following ways:
• 1. Salbutamol → Stimulates β2 receptors of the bronchial smooth muscle → Stimulation of the Adenylate Cyclase enzyme → Increased intracellular cyclic-AMP (also reduction of the intracellular calcium) → Smooth muscle relaxation → Bronchodilatation occurs.
• 2. Salbutamol → Acts on the β2 receptor of the mast cell → ↑ c-AMP production → Stabilization of the mast cell membrane → No Histamine release → No bronchoconstriction.
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• 3. Salbutamol increases the muco-ciliary action of the lung.
• 4. Decreases micro-vascular permeability of the lung.
• Inihbit release of bronchoconstircting mediators from mast cell.
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Uses:Used in asthma.
Side effects of long-acting bronchodilators include:
• Increased heart rate• Headache• Anxiety• Tremor
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• Pharmacokinetics• Salbutamol is a direct-acting
sympathomimetic with β-adrenergic activity and selective action on β2 receptors, producing bronchodilating effects. It also decreases uterine contractility.
OnsetInhalation: 5-15 min; oral: 30 min.
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• DurationInhalation: 3-6 hr; oral: 8 hr; modified-release preparation: 12 hr.AbsorptionReadily absorbed from the GI tract.MetabolismHepatic and in the gut wall.ExcretionVia the urine as metabolites and unchanged drug. Some excretion in the faeces.
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Methyl Xanthine
Drugs
Theophylline
Theobromine
Caffine
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Xanthine derivatives:• Chemically they are purine having
similar chemical structure with adenine and uric acid. Wide spreads pharmacological action so, not used. These drugs have low therapeutic index. Increases intra-cellular cyclic-AMP concentration within the bronchial smooth muscle cell.
• Theophylline is the prototype, it is water insoluble but it’s salts are water soluble
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Mechanism of Action of Theophylline
• 1. Combines with the adenosine receptor (PI) and acts as antagonist of adenosine thus prevents it to cause contraction of the bronchial smooth muscle.
• 2. Combines and inactivates phospho-diesterase enzyme and degradation of the cyclic-AMP stops. C-AMP accumulates in the bronchial smooth muscle and causes bronchodilatation. C-AMP has negative effect on the release of the calcium from the endoplasmic reticulum.
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Pharmacological effects:• Lung: bronchodilatation• CNS: Cortical stimulation, excitement,
↓ mental exhaustion and fatigue. Loss of sleep. Stimulate medullary respiratory and vomiting center.
• CVS : Positive ionotropic and chronotropic effects. ↑ CO, ↑ HR, ↑ force of contraction. At large doses it causes cerebral vaso-constriction. In high level—toxicity—cardiac arrhythmia, tachycardia
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• Kidney: Diabetic action. ↑ renal blood supply and GFR. ↓ Na+ and other electrolyte absorption.
• Skeletal muscle: Diaphragmatic contraction is stimulated. ↓ fatigue of the skeletal muscle. Causes tremor.
• GIT : ↑ gastric acid secretion.
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Adverse effects of Theophylline• Therapeutic index is very low
• Nausea, vomiting• Therapeutic blood level is
0.2-2mg/100ml• Nausea, vomiting may appear in
<2mg/100ml• Convulsion in >4mg/100ml• Cardiac arrhythmia may occur• (total dose should be given at least in
20min)
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Points Salbutamol Aminophylline
Mechanism of Action
Selective stimulation of the β2 adrenoceptor of bronchial smooth muscle and causes bronchodilatation
Competitive inhibition of the bronchial adenosine receptors and causes bronchodilatation
Onset of action
Slower Rapid
Duration of action
Longer Shorter
Therapeutic index
Larger Narrow
In acute asthma
Suitable in inhaler form
Suitable in IV form
Drug of choice
Mildest asthmatic with intermittent attack
Severe acute asthma and chronic asthma
Side effects Tremor, headache, cardiac arrhythmia
Headache, vomiting
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Antimuscarinic Agents
Ipratropium bromide
Tiotropium(selective
antimuscarinic)Atropine
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Anticholinergic drugs• Atropine is the prototype, cheap,
causes bronchodilatation.Mechanism of Action:• Vagal nerve innervation→ acetyle
choline→ muscarinic receptor→ bronchoconstriction
• Anticholinergics act here by inhibiting the muscarinic receptors ↑
• Uses:• Used in asthma
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Adverse effects of Atropine• Can cross the BBB and go to the CNS.• Mouth dryness.• Destroy the cilia of the respiratory tract
—prone to infection.• an allergic reaction (swelling of your
lips, tongue, or face, difficulty breathing, closing of your throat, or hives);
• an irregular or fast heart rate;• rash or flushing; or• eye pain.
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Corticosteroid
Beclomethasone
Budesonide
Mometasone
Ciclesonide
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Corticosteroids (MOA)• They: inhibit chemical mediators,
whether these are performed, like histamine, or newly formed, like arachidonic acid metabolites (prostaglandins and leukotrienes) or the platelet-activating factor (PAF); restore the sensitivity of beta-adrenergic receptors to sympathomimetic drugs; exert a powerful anti-inflammatory effect, notably reducing bronchial mucus secretion; reduce bronchial hyperreactivity and modify the bronchial response to bronchoconstrictors; act on respiratory function and gas exchanges.
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• Many effects of corticosteroids in asthma involve the synthesis of proteins, such as lipomodulin (or macrocortin) which inhibits phospholipase A2, a key-enzyme in the synthesis of numerous chemical mediators derived from membrane phospholipids. The multiple effects of corticosteroids account for their broad spectrum of activity and their effectiveness against both acute and chronic manifestations of asthma.
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Uses:• Inhaled glucocorticoids are the
second-line treatment for asthma.• Glucocorticoids may be used in low
doses in adrenal insufficiency. In much higher doses, oral or inhaled glucocorticoids are used to suppress various allergic, inflammatory, and autoimmune disorders
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Side effects• Growth failure, delayed puberty• Increased plasma amino acids,
increased urea formation, negative nitrogen balance
• Excitatory effect on central nervous system (euphoria, psychosis)
• Glaucoma due to increased cranial pressure
• Cataracts
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Possible side effects of long-term oral corticosteroid use include:
• Water retention• Bruising• Puffy face• Increased appetite• Weight gain• Stomach irritation• Mood changes• Fractures
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Leukotriene pathway inhibitors
Montelukast
Zileuton
Zafirlukast
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Leukotriene:• The leukotriene receptor
antagonists are among the most prescribed drugs for the management of asthma, used both for treatment and prevention of acute asthmatic attacks. This class of drugs acts by binding to cysteinyl leukotriene receptors (CysLT1 and CysLT2) and blocking their activation and the subsequent inflammatory cascade which cause the symptoms commonly associated with asthma and allergic rhinitis.
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Mchanism of Action: • Leukotrienes are synthesized in response to
many triggers, including receptor activation, antigen-antibody interaction, physical stimuli such as cold, and any stimulation that increases intercellular calcium.These potent inflammatory mediators promote neutrophil-endothelial interactions, inducing bronchoconstriction and enhancing airway hyperresponsiveness. They also stimulate smooth muscle hypertrophy, mucus hypersecretion, and the influx of eosinophils into airway tissues therefore, inhibition of leukotrienes potentially plays an important role in the treatment of asthma and other allergic conditions such as allergic rhinitis, atopic dermatitis, and chronic urticaria
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• Leukotriene receptor antagonists, called LTRAs for short, are a class of oral medication that is non-steroidal. They may also be referred to as anti-inflammatory bronchoconstriction preventors. LTRAs work by blocking a chemical reaction that can lead to inflammation in the airways. Although not preferred first choice therapy, LTRAs can be tried when an inhaled steroid can not, or will not, be used, or if the dose cannot be increased
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Uses:• It is used in Asthama.
• Side Effects:• Elevation in serum hepatic enzyme• Nausea• Headache• Inhibitors of cytochrome P450.
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Cromolyn
Nedocromil
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Mechanism of action:• Alter the function of delayed
chloride channels in cell membrane.
• Inhibiting cell activation • This action thought to mediate
inhibition of cough.• Inhibit the function of cells other
then mast cell degranulation and release of histamine.
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Clinical uses:• Used for non seasonal asthma• Particularly used in children and
pragnant woman.Side effects:• Throat irritation • Cough• Mouth dryness• Chest tightness• Wheezing
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Other DrugsAnti-IgE
Monoclonal Antibodies
Omalizumab
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Anti Immunoglobulin E (Anti-IgE) Therapy
• Anti-IgE treatment might be recommended if you have allergic asthma and you keep experiencing persistent symptoms despite taking your controller medications.
• If you have allergic asthma (about 60% of asthma is caused by allergy), your symptoms are triggered when you inhale certain allergens in the air.
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MOA:• These allergens cause a chain
reaction that leads to inflammation in the lungs.
• While inhaled steroids work by treating and reducing the inflammation, anti-IgE therapy works by keeping inflammation from developing in the first place. It does so by blocking immunoglobulin E, a substance in the body that is one of the underlying causes of inflammation in allergic asthma.
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• Anti-IgE therapy is only available by prescription. Unlike other asthma medications, it is not administered by pill or by inhaler. It needs to be injected once every two or four weeks by a doctor or other trained healthcare professional.
• The only anti-IgE therapy available in Canada is omalizumab.
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Side Effects:• Skin irritation • Reaction at the site of the injection • Respiratory tract infections (e.g.,
common cold).
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Combination Medications• Some pharmaceutical
manufacturers have combined two controller medications into one inhaler. These inhalers are referred to as "Combination Medications".
• Combination medications contain both an inhaled long-acting bronchodilator (LABA) and an inhaled corticosteroid.
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Combination Medications
Corticosteroids Long-Acting Bronchodilators
Symbicort® Budesonide (Pumicort®)
Formoterol (Oxeze®)
Advair® Fluticasone (Flovent®)
Salmeterol (Severent®)
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• This means that two areas of asthma can be effectively treated at the same time the bronchodilator works by widening your airways, making it easier for you to breathe, and the inhaled steroid reduces and prevents inflammation of your airways.
• Recent studies show that many people with asthma find that combination medications give them better control and are convenient to use.
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Possible side effects of combination medications include:• Rapid heart beat
• Tremor or nervousness• Cough, throat irritation or
hoarseness