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GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability
BACKGROUND AND PURPOSE: TREK two‐pore‐domain potassium (K(2P)) channels play a critical role in regulating the excitability of somatosensory nociceptive neurons and are important mediators of pain perception. An understanding of the roles of TREK channels in pain perception and, indeed, in other pat...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980259/ https://www.ncbi.nlm.nih.gov/pubmed/29150838 http://dx.doi.org/10.1111/bph.14098 |
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author | Loucif, Alexandre J C Saintot, Pierre‐Philippe Liu, Jia Antonio, Brett M Zellmer, Shannon G Yoger, Katrina Veale, Emma L Wilbrey, Anna Omoto, Kiyoyuki Cao, Lishuang Gutteridge, Alex Castle, Neil A Stevens, Edward B Mathie, Alistair |
author_facet | Loucif, Alexandre J C Saintot, Pierre‐Philippe Liu, Jia Antonio, Brett M Zellmer, Shannon G Yoger, Katrina Veale, Emma L Wilbrey, Anna Omoto, Kiyoyuki Cao, Lishuang Gutteridge, Alex Castle, Neil A Stevens, Edward B Mathie, Alistair |
author_sort | Loucif, Alexandre J C |
collection | PubMed |
description | BACKGROUND AND PURPOSE: TREK two‐pore‐domain potassium (K(2P)) channels play a critical role in regulating the excitability of somatosensory nociceptive neurons and are important mediators of pain perception. An understanding of the roles of TREK channels in pain perception and, indeed, in other pathophysiological conditions, has been severely hampered by the lack of potent and/or selective activators and inhibitors. In this study, we describe a new, selective opener of TREK channels, GI‐530159. EXPERIMENTAL APPROACH: The effect of GI‐530159 on TREK channels was demonstrated using (86)Rb efflux assays, whole‐cell and single‐channel patch‐clamp recordings from recombinant TREK channels. The expression of K(2P)2.1 (TREK1), K(2P)10.1 (TREK2) and K(2P)4.1 (TRAAK) channels was determined using transcriptome analysis from single dorsal root ganglion (DRG) cells. Current‐clamp recordings from cultured rat DRG neurons were used to measure the effect of GI‐530159 on neuronal excitability. KEY RESULTS: For recombinant human TREK1 channels, GI‐530159 had similar low EC(50) values in Rb efflux experiments and electrophysiological recordings. It activated TREK2 channels, but it had no detectable action on TRAAK channels nor any significant effect on other K channels tested. Current‐clamp recordings from cultured rat DRG neurones showed that application of GI‐530159 at 1 μM resulted in a significant reduction in firing frequency and a small hyperpolarization of resting membrane potential. CONCLUSIONS AND IMPLICATIONS: This study provides pharmacological evidence for the presence of mechanosensitive TREK K(2P) channels in sensory neurones and suggests that development of selective K(2P) channel openers like GI‐530159 could aid in the development of novel analgesic agents. LINKED ARTICLES: This article is part of a themed section on Recent Advances in Targeting Ion Channels to Treat Chronic Pain. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.12/issuetoc |
format | Online Article Text |
id | pubmed-5980259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59802592018-06-06 GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability Loucif, Alexandre J C Saintot, Pierre‐Philippe Liu, Jia Antonio, Brett M Zellmer, Shannon G Yoger, Katrina Veale, Emma L Wilbrey, Anna Omoto, Kiyoyuki Cao, Lishuang Gutteridge, Alex Castle, Neil A Stevens, Edward B Mathie, Alistair Br J Pharmacol Themed Section: Research Papers BACKGROUND AND PURPOSE: TREK two‐pore‐domain potassium (K(2P)) channels play a critical role in regulating the excitability of somatosensory nociceptive neurons and are important mediators of pain perception. An understanding of the roles of TREK channels in pain perception and, indeed, in other pathophysiological conditions, has been severely hampered by the lack of potent and/or selective activators and inhibitors. In this study, we describe a new, selective opener of TREK channels, GI‐530159. EXPERIMENTAL APPROACH: The effect of GI‐530159 on TREK channels was demonstrated using (86)Rb efflux assays, whole‐cell and single‐channel patch‐clamp recordings from recombinant TREK channels. The expression of K(2P)2.1 (TREK1), K(2P)10.1 (TREK2) and K(2P)4.1 (TRAAK) channels was determined using transcriptome analysis from single dorsal root ganglion (DRG) cells. Current‐clamp recordings from cultured rat DRG neurons were used to measure the effect of GI‐530159 on neuronal excitability. KEY RESULTS: For recombinant human TREK1 channels, GI‐530159 had similar low EC(50) values in Rb efflux experiments and electrophysiological recordings. It activated TREK2 channels, but it had no detectable action on TRAAK channels nor any significant effect on other K channels tested. Current‐clamp recordings from cultured rat DRG neurones showed that application of GI‐530159 at 1 μM resulted in a significant reduction in firing frequency and a small hyperpolarization of resting membrane potential. CONCLUSIONS AND IMPLICATIONS: This study provides pharmacological evidence for the presence of mechanosensitive TREK K(2P) channels in sensory neurones and suggests that development of selective K(2P) channel openers like GI‐530159 could aid in the development of novel analgesic agents. LINKED ARTICLES: This article is part of a themed section on Recent Advances in Targeting Ion Channels to Treat Chronic Pain. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.12/issuetoc John Wiley and Sons Inc. 2017-12-29 2018-06 /pmc/articles/PMC5980259/ /pubmed/29150838 http://dx.doi.org/10.1111/bph.14098 Text en © 2017 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Themed Section: Research Papers Loucif, Alexandre J C Saintot, Pierre‐Philippe Liu, Jia Antonio, Brett M Zellmer, Shannon G Yoger, Katrina Veale, Emma L Wilbrey, Anna Omoto, Kiyoyuki Cao, Lishuang Gutteridge, Alex Castle, Neil A Stevens, Edward B Mathie, Alistair GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability |
title | GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability |
title_full | GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability |
title_fullStr | GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability |
title_full_unstemmed | GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability |
title_short | GI‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (K(2P)) channel opener, reduces rat dorsal root ganglion neuron excitability |
title_sort | gi‐530159, a novel, selective, mechanosensitive two‐pore‐domain potassium (k(2p)) channel opener, reduces rat dorsal root ganglion neuron excitability |
topic | Themed Section: Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980259/ https://www.ncbi.nlm.nih.gov/pubmed/29150838 http://dx.doi.org/10.1111/bph.14098 |
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