Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2530105 | Current Opinion in Pharmacology | 2011 | 10 Pages |
Inhalation or aspiration of acid solution evokes airway defense responses such as cough and reflex bronchoconstriction, resulting from activation of vagal bronchopulmonary C-fibers and Aδ afferents. The stimulatory effect of hydrogen ion on these sensory nerves is generated by activation of two major types of ion channels expressed in these neurons: a rapidly activating and inactivating current mediated through ASICs, and a slow sustaining current via activation of TRPV1. Recent studies have shown that these acid-evoked responses are elevated during airway inflammatory reaction, revealing the potential convergence of a wide array of inflammatory signaling on these ion channels. Since pH in the airway fluid drops substantially in patients with inflammatory airway diseases, these heightened stimulatory effects of acid on airway sensory nerves may play a part in the manifestation of airway irritation and excessive cough under those pathophysiological conditions.
► Acid stimulates airway C-fibers and Aδ afferents, and causes airway irritation. ► This stimulatory effect is generated by activation of both ASIC and TRPV1 channels. ► Acid-evoked airway irritation is enhanced during airway inflammatory reaction.