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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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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. |
format | Online Article Text |
id | pubmed-9578445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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