Related Experiment Video
Updated: May 28, 2026

Absorption of Nasal and Bronchial Fluids: Precision Sampling of the Human Respiratory Mucosa and Laboratory Processing of Samples
Published on: January 21, 2018
Nasopharyngeal prostaglandin E(2) in infant bronchiolitis
Kim M Griggs1, Kevin D Forsyth, Dani-Louise Dixon
1Department of Critical Care Medicine, Flinders University, Adelaide, Australia.
Prostaglandin E(2) in infant bronchiolitis airways did not predict disease severity or recurrent wheeze. Further research is needed to determine if Prostaglandin E(2) is a viable therapeutic target for bronchiolitis.
Area of Science:
- Pediatric Respiratory Medicine
- Immunology
- Molecular Medicine
Background:
- Severe bronchiolitis can lead to recurrent childhood wheeze, with mucosal inflammation and immune activation implicated.
- Prostaglandin E(2) (PGE(2)) is a potential therapeutic target for bronchiolitis treatment and prevention of airway hyperresponsiveness.
Purpose of the Study:
- To investigate the role of PGE(2) in the airways of infants hospitalized with bronchiolitis.
- To assess the relationship between airway PGE(2) levels and disease severity, clinical course, and long-term outcomes.
Main Methods:
- Nasopharyngeal aspirates (NPA) were collected from 18 infants within 12 hours of admission.
- Enzyme immunoassays were used to measure PGE(2), interleukin-10 (IL-10), and IL-12, and cyclooxygenase (COX) 1 and 2 activity.
Main Results:
- NPA PGE(2) concentration correlated with preadmission illness duration but not with disease severity, viral cause, or IL-10 levels.
- NPA COX 1 and 2 activity and IL-12 levels were below detection limits.
- Neither NPA PGE(2) nor disease severity predicted the development of recurrent wheeze over 3 years post-bronchiolitis.
Conclusions:
- Nasopharyngeal PGE(2) at hospital admission does not appear to be a direct cause, diagnostic marker for severity, or prognostic indicator for recurrent wheeze in infant bronchiolitis.
- Larger cohort studies are necessary to definitively evaluate PGE(2) as a therapeutic target for bronchiolitis.
Related Concept Videos
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
Respiratory Syncytial Virus Disease
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Upper Respiratory Drugs: Antitussives, Expectorants, and Mucolytics
Antitussives include codeine, dextromethorphan (Robitussin), and benzonatate (Tessalon). Codeine and dextromethorphan exert their effects centrally by suppressing the cough reflex center in the medulla. Benzonatate operates peripherally within the respiratory tract by anesthetizing...
Breathing
Epistaxis
Etiology
Possible causes of this condition include high blood pressure, trauma, low humidity, upper respiratory tract infections, allergies, foreign bodies, nasal inhalation of corticosteroids or illicit drugs, excessive use of decongestant nasal sprays, facial or nasal surgery, anatomic malformation, tumors, or systemic...
