Background And Purpose: The purpose of this study was to determine the role of Na 1.7 in action potential conduction in C-fibres in the bronchial branches of the human vagus nerve.
Experimental Approach: Bronchial branches of the vagus nerve were dissected from human donor tissue. The C-wave of the electrically evoked compound action potential was quantified in the absence and presence of increasing concentrations of the selective Na 1.7 blocking drugs, PF-05089771 and ST-2262, as well as the Na 1.1, 1.2, and 1.3 blocking drug ICA121-431. The efficacy and potency of these inhibitors were compared to the standard Na 1 blocker, tetrodotoxin. We then compared the relative potencies of the Na 1 blockers in inhibiting the C-wave of the compound action potential, with their ability to inhibit parasympathetic cholinergic contraction of human isolated bronchi, a response previously shown to be strictly dependent on Na 1.7 channels.
Key Results: The selective Na 1.7 blockers inhibited the C-wave of the compound action potential with potencies similar to that observed in the Na 1.7 bronchial contractions assay. Using rt-PCR, we noted that Na 1.7 mRNA was strongly expressed and transported down the vagus nerve bundles.
Conclusions And Implications: Na 1.7 blockers can prevent action potential conduction in the majority of vagal C-fibres arising from human bronchi. Blockers of Na 1.7 channels may therefore have value in inhibiting the responses to excessive airway C-fibre activation in inflammatory airway disease, responses that include coughing as well as reflex bronchoconstriction and secretions.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1111/bph.15686 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!