Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve. Issue 1 (31st December 2022)

• Record Type: Journal Article
• Authors: Klein, Rebecca M.; Layton, Mark E.; Regan, Hillary; Regan, Christopher P.; Li, Yuxing; Filzen, Tracey; Cato, Matt; Clements, Michelle K.; Wang, Jixin; Sanoja, Raul; Greshock, Thomas J.; Roecker, Anthony J.; Pero, Joseph E.; Kim, Ron; Burgey, Christopher; John, Christopher T.; Wang, Ying-Hong; Bhandari, Neetesh; Struyk, Arie; Kraus, Richard L.; Henze, Darrell A.; Houghton, Andrea K.
• Is Part Of: Channels. Volume 16:Issue 1(2022)
• Page Start: 230
• Page End: 243
• Publication Date: 2022-12-31
• Subjects: Sodium channel inhibitor -- respiration -- selectivity -- phrenic nerve; Ion channels -- Periodicals; 572.3
• DOI: 10.1080/19336950.2022.2122309
• Languages: English
• ISSNs: 1933-6950

Abstract

ABSTRACT: As part of a drug discovery effort to identify potent inhibitors of NaV1.7 for the treatment of pain, we observed that inhibitors produced unexpected cardiovascular and respiratory effects in vivo. Specifically, inhibitors administered to rodents produced changes in cardiovascular parameters and respiratory cessation. We sought to determine the mechanism of the in vivo adverse effects by studying the selectivity of the compounds on NaV1.5, NaV1.4, and NaV1.6 in in vitro and ex vivo assays. Inhibitors lacking sufficient NaV1.7 selectivity over NaV1.6 were associated with respiratory cessation after in vivo administration to rodents. Effects on respiratory rate in rats were consistent with effects in an ex vivo hemisected rat diaphragm model and in vitro NaV1.6 potency. Furthermore, direct blockade of the phrenic nerve signaling was observed at exposures known to cause respiratory cessation in rats. Collectively, these results support a significant role for NaV1.6 in phrenic nerve signaling and respiratory function.