Bronchodilators: Leukotriene antagonists and methylxanthines

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Bronchodilators: Leukotriene antagonists and methylxanthines

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Gastroesophageal reflux disease (GERD)
Gastroesophageal reflux disease (GERD): Clinical
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Asthma: Clinical
Asthma
Asthma: Information for patients and families (The Primary School)
Chronic kidney disease
Chronic kidney disease: Clinical
Anemia of chronic disease
Kidney stones
Acute kidney injury: Clinical
Anatomy of the abdominal viscera: Kidneys, ureters and suprarenal glands
Prerenal azotemia
Renal system anatomy and physiology
Renal azotemia
Postrenal azotemia
Renal failure: Pathology review
Taking a good patient history
Using an inhaler: Information for patients and families
Macrocytic anemia: Pathology review
Anemia: Clinical
Aplastic anemia
Extrinsic hemolytic normocytic anemia: Pathology review
Microcytic anemia: Pathology review
Autoimmune hemolytic anemia
Non-hemolytic normocytic anemia: Pathology review
Iron deficiency anemia
Intrinsic hemolytic normocytic anemia: Pathology review
Megaloblastic anemia
Obstructive lung diseases: Pathology review
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Cholinomimetics: Direct agonists
General anesthetics
Pulmonary corticosteroids and mast cell inhibitors
Isolated primary immunoglobulin M deficiency
Muscarinic antagonists
Cell-mediated immunity of CD4 cells
Adrenergic antagonists: Beta blockers
Non-steroidal anti-inflammatory drugs
Chronic obstructive pulmonary disease (COPD): Clinical
Clinical Skills: Using a metered-dose inhaler
Psychomotor stimulants
Tobacco use disorder
Cholinomimetics: Indirect agonists (anticholinesterases)
Sympathomimetics: Direct agonists
Jaundice
Neonatal jaundice: Clinical
Jaundice: Clinical
Jaundice: Pathology review
Cholestatic liver disease
Cirrhosis
Cirrhosis: Pathology review
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Cirrhosis: Clinical
Urinary tract infections: Clinical
Urinary incontinence
Urinary incontinence: Pathology review
Renal and urinary tract masses: Pathology review
Bladder exstrophy
Neurogenic bladder
Elimination disorders: Clinical
Cholinergic receptors
Inflammatory bowel disease: Pathology review
Inflammatory bowel disease: Clinical
Irritable bowel syndrome
Small bowel ischemia and infarction
Bowel obstruction: Clinical
Diarrhea: Clinical
Electrolyte disturbances: Pathology review
Laxatives and cathartics
Acetaminophen (Paracetamol)
Peptic ulcer
Peptic ulcers and stomach cancer: Clinical
Gastrointestinal bleeding: Pathology review
Ulcerative colitis
Liver histology
Alcohol-associated liver disease
Liver anatomy and physiology
Non-alcoholic fatty liver disease
Anatomy of the abdominal viscera: Liver, biliary ducts and gallbladder
Hepatic encephalopathy
Gastrointestinal system anatomy and physiology
Bowel obstruction
Enteric nervous system
Pulmonary hypertension
Pulmonary edema
Osteoarthritis
Rheumatoid arthritis and osteoarthritis: Pathology review
Joint pain: Clinical
Gout
Gout and pseudogout: Pathology review
Antigout medications
Glucocorticoids
Osmotic diuretics
Loop diuretics
Potassium sparing diuretics
Thiazide and thiazide-like diuretics
Diabetic nephropathy
Hyperkalemia: Clinical
Hypokalemia: Clinical
Metabolic and respiratory alkalosis: Clinical
Hyponatremia
Metabolic alkalosis
Hypernatremia: Clinical
Hypertension: Clinical
Hyperphosphatemia
Hypokalemia
Hyponatremia: Clinical
Hypernatremia
Hypermagnesemia
Hyperkalemia
Hypercalcemia
Portal hypertension
Rheumatoid arthritis: Clinical
Rheumatoid arthritis
Hypocalcemia
Hypoxia
Hypomagnesemia
Hypophosphatemia
Orthostatic hypotension

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Bronchodilators: Leukotriene antagonists and methylxanthines

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A 32-year-old woman is brought to the emergency department because of a generalized tonic-clonic seizure. She does not have a prior history of seizure disorder. Past medical history is significant for severe persistent asthma, hypertension, and hyperlipidemia. Five days ago, the patient was started on ciprofloxacin for a urinary tract infection. Her other medications include inhaled fluticasone/salmeterol combination, theophylline, lisinopril, and hydrochlorothiazide. Her BMI is 37 kg/m2. Her temperature is 37°C (98.6°F), pulse is 115/min, respirations are 15/min, and blood pressure is 110/65 mmHg. Physical examination is unremarkable. Which medications is the most likely cause of this patient’s presentation?

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In obstructive lung diseases like asthma, individuals suffer from reversible narrowing of the airways, medications like bronchodilators are helpful in keeping the airways open.

Now, based on their mechanism of action, bronchodilators can be broadly divided into four main groups; β2-agonists, muscarinic antagonists, leukotrienes antagonist and methylxanthines.

In this video, we’ll focus on the leukotriene modifying agents and methylxanthines.

So, if we take a look at the lungs, you’ve got the trachea, which branches off into right and left bronchi, and then continues to branch into thousands of bronchioles.

In the bronchioles you’ve got the lumen, the mucosa, which includes the inner lining of epithelial cells, as well as the lamina propria which contains many cells like the type 2 helper T cells, B cells, and mast cells.

Surrounding the lamina propria, there is a layer of smooth muscles and submucosa.

The submucosal layer contains mucus-secreting glands and blood vessels.

Now, the molecular pathway that leads to asthma is actually pretty complex but it is often initiated by an environmental trigger.

Allergens from environmental triggers, like air pollutants or cigarette smoke, are picked up by dendritic cells which present them to a type 2 helper T cell or Th2 cell in the lamina propria. These cells then produce cytokines like IL-4 and IL-5 which causes the inflammatory response.

IL-4 is especially important because it leads to the production of IgE antibodies by B cells, and these antibodies bind to FcεR1 receptors on mast cells to activate them.

These mast cells use an enzyme called phospholipase A2 to take membrane phospholipids and make a 20 carbon polyunsaturated fatty acid called arachidonic acid.

Arachidonic acid is then metabolized by two important enzymes: one is cyclooxygenase-2 or COX-2, which makes prostaglandins, another one is 5-lipoxygenase or 5-LOX, which makes leukotrienes.

Now, IL-5 on the other hand, activates eosinophils, which promote an immune response by releasing more cytokines and leukotrienes.

Minutes after exposure to the allergen, phospholipase A2 gets activated inside the mast cells, which results in the synthesis and release of leukotrienes and the prostaglandins.

Leukotrienes bind with the leukotriene receptors on the bronchial smooth muscles and cause them to contract. They also bind to receptors on the mucous glands to increase mucus secretion.

Similarly, prostaglandins also bind to their receptors in smooth muscles and mucus glands to cause a similar effect. These mediators also increase the vascular permeability in the airways and attract more immune cells to the area.

The combination of inflammation and bronchospasm cause obstruction of the airway which leads to symptoms like coughing, chest tightness, dyspnea, or difficulty breathing, and wheezing, which is a high-pitched whistling sound during exhalation.

Chronic inflammation also makes the respiratory tract more sensitive to allergens, so these symptoms become easier to trigger.

In this video, we’ll focus on the management of smooth muscle spasms, as relieving the spasms will help in opening up the narrowed airways. Now, to do that, the role of bronchodilators like leukotriene modifying agents and methylxanthines is very important.

Let’s start with the leukotriene modifying agents. These medications can be divided into two broad groups. One is leukotriene receptor antagonists, also known as “cysteinyl leukotriene receptor antagonists”. The other group is leukotriene synthesis inhibitors, which are also known as 5-lipoxygenase inhibitor.

Leukotriene receptor antagonists like montelukast and zafirlukast are peroral medications that bind to the leukotriene receptors in the smooth muscles of the respiratory airways and prevent leukotriene from binding. This weakens smooth muscle contraction in the respiratory tract, decreases mucus secretion, and reduces inflammation.

Since they are taken peroral, they have a slower onset of action compared to inhaled bronchodilators like albuterol, which is why they are used for asthma prophylaxis and not during an acute asthma attack.

They are especially effective in preventing exercise or aspirin induced asthma.

Since leukotriene receptor antagonists have mild, nonspecific side effects like headache and rash, they are given in combination with other asthma medications like corticosteroids, which can cause immunosuppression, and long acting beta agonists, which can cause arrhythmias.

This will lower the necessary dose of these more dangerous medications, which makes montelukast and zafirlukast great supportive medications.

Next, let’s move on to the leukotriene synthesis inhibitors like zileuton, which is also peroral.

After absorption, it enters immune cells like mast cells and inhibits the enzyme 5-lipoxygenase, which stops the synthesis of leukotriene from arachidonic acid.

Sources

  1. "Katzung & Trevor's Pharmacology Examination and Board Review,12th Edition" McGraw-Hill Education / Medical (2018)
  2. "Rang and Dale's Pharmacology" Elsevier (2019)
  3. "Goodman and Gilman's The Pharmacological Basis of Therapeutics, 13th Edition" McGraw-Hill Education / Medical (2017)
  4. "Triple therapy (ICS/LABA/LAMA) in COPD: time for a reappraisal" International Journal of Chronic Obstructive Pulmonary Disease (2018)
  5. "Exacerbations of COPD" International Journal of Chronic Obstructive Pulmonary Disease (2016)
  6. "Medication Regimens for Managing Acute Asthma" Respiratory Care (2018)