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Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve

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 res...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578445/
https://www.ncbi.nlm.nih.gov/pubmed/36239534
http://dx.doi.org/10.1080/19336950.2022.2122309
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author 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.
author_facet 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.
author_sort Klein, Rebecca M.
collection PubMed
description 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.
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spelling pubmed-95784452022-10-19 Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve 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. Channels (Austin) Research Paper 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. Taylor & Francis 2022-10-14 /pmc/articles/PMC9578445/ /pubmed/36239534 http://dx.doi.org/10.1080/19336950.2022.2122309 Text en © 2022 Merck & Co, Inc. Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
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.
Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve
title Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve
title_full Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve
title_fullStr Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve
title_full_unstemmed Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve
title_short Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve
title_sort association of respiratory failure with inhibition of nav1.6 in the phrenic nerve
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578445/
https://www.ncbi.nlm.nih.gov/pubmed/36239534
http://dx.doi.org/10.1080/19336950.2022.2122309
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