Indomethacin Abolishes the Potentiation Effect of Testosterone on the Relaxation Induced by Salbutamol and Theophylline by Directly Blocking the K+ Channels in Airway Smooth Muscle
Jorge Reyes-García, Abril Carbajal-García, Verónica Díaz-Hernández, María F. Casas-Hernández, Luis M. Montaño

TL;DR
Indomethacin blocks the muscle-relaxing effects of testosterone in airways by inhibiting potassium channels, which could worsen asthma symptoms in young males.
Contribution
Indomethacin uniquely inhibits both K+ channels and prostaglandin synthesis, unlike other NSAIDs.
Findings
Indomethacin fully abolishes testosterone-enhanced relaxation in airway smooth muscle.
Indomethacin inhibits KV and BKCa K+ currents potentiated by testosterone.
Indomethacin's dual mechanism may counteract testosterone's protective effects in asthma.
Abstract
Indomethacin, ibuprofen, and acetylsalicylic acid (ASA) are non-steroidal anti-inflammatory drugs (NSAIDs) that inhibit prostaglandin (PG) synthesis. Previous studies in airway smooth muscle demonstrated that chronic exposure to testosterone (TES, 40 nM) enhances the relaxation induced by salbutamol and theophylline due to K+ channel increment, without modifying cyclooxygenase expression. This study examines how indomethacin, ibuprofen, and ASA affect K+ currents and the relaxation response to these bronchodilators. In organ baths, tracheas from young male guinea pigs chronically (48 h) treated with 40 nM TES showed increased relaxation to salbutamol and theophylline, which was completely abolished by indomethacin. Patch-clamp recordings revealed that TES increased salbutamol- and theophylline-induced K+ currents, and only indomethacin fully inhibited this potentiation; ibuprofen and…
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Taxonomy
TopicsAsthma and respiratory diseases · Pharmacological Effects and Assays · Ion channel regulation and function
