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Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells
Type 1 cannabinoid receptors (CB1Rs) are widely expressed in the vertebrate retina, but the role of endocannabinoids in vision is not fully understood. Here, we identified a novel mechanism underlying a CB1R-mediated increase in retinal ganglion cell (RGC) intrinsic excitability acting through AMPK-...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987138/ https://www.ncbi.nlm.nih.gov/pubmed/27501334 http://dx.doi.org/10.7554/eLife.15932 |
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author | Miraucourt, Loïs S Tsui, Jennifer Gobert, Delphine Desjardins, Jean-François Schohl, Anne Sild, Mari Spratt, Perry Castonguay, Annie De Koninck, Yves Marsh-Armstrong, Nicholas Wiseman, Paul W Ruthazer, Edward S |
author_facet | Miraucourt, Loïs S Tsui, Jennifer Gobert, Delphine Desjardins, Jean-François Schohl, Anne Sild, Mari Spratt, Perry Castonguay, Annie De Koninck, Yves Marsh-Armstrong, Nicholas Wiseman, Paul W Ruthazer, Edward S |
author_sort | Miraucourt, Loïs S |
collection | PubMed |
description | Type 1 cannabinoid receptors (CB1Rs) are widely expressed in the vertebrate retina, but the role of endocannabinoids in vision is not fully understood. Here, we identified a novel mechanism underlying a CB1R-mediated increase in retinal ganglion cell (RGC) intrinsic excitability acting through AMPK-dependent inhibition of NKCC1 activity. Clomeleon imaging and patch clamp recordings revealed that inhibition of NKCC1 downstream of CB1R activation reduces intracellular Cl(−) levels in RGCs, hyperpolarizing the resting membrane potential. We confirmed that such hyperpolarization enhances RGC action potential firing in response to subsequent depolarization, consistent with the increased intrinsic excitability of RGCs observed with CB1R activation. Using a dot avoidance assay in freely swimming Xenopus tadpoles, we demonstrate that CB1R activation markedly improves visual contrast sensitivity under low-light conditions. These results highlight a role for endocannabinoids in vision and present a novel mechanism for cannabinoid modulation of neuronal activity through Cl(−) regulation. DOI: http://dx.doi.org/10.7554/eLife.15932.001 |
format | Online Article Text |
id | pubmed-4987138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49871382016-08-23 Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells Miraucourt, Loïs S Tsui, Jennifer Gobert, Delphine Desjardins, Jean-François Schohl, Anne Sild, Mari Spratt, Perry Castonguay, Annie De Koninck, Yves Marsh-Armstrong, Nicholas Wiseman, Paul W Ruthazer, Edward S eLife Neuroscience Type 1 cannabinoid receptors (CB1Rs) are widely expressed in the vertebrate retina, but the role of endocannabinoids in vision is not fully understood. Here, we identified a novel mechanism underlying a CB1R-mediated increase in retinal ganglion cell (RGC) intrinsic excitability acting through AMPK-dependent inhibition of NKCC1 activity. Clomeleon imaging and patch clamp recordings revealed that inhibition of NKCC1 downstream of CB1R activation reduces intracellular Cl(−) levels in RGCs, hyperpolarizing the resting membrane potential. We confirmed that such hyperpolarization enhances RGC action potential firing in response to subsequent depolarization, consistent with the increased intrinsic excitability of RGCs observed with CB1R activation. Using a dot avoidance assay in freely swimming Xenopus tadpoles, we demonstrate that CB1R activation markedly improves visual contrast sensitivity under low-light conditions. These results highlight a role for endocannabinoids in vision and present a novel mechanism for cannabinoid modulation of neuronal activity through Cl(−) regulation. DOI: http://dx.doi.org/10.7554/eLife.15932.001 eLife Sciences Publications, Ltd 2016-08-08 /pmc/articles/PMC4987138/ /pubmed/27501334 http://dx.doi.org/10.7554/eLife.15932 Text en © 2016, Miraucourt et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Miraucourt, Loïs S Tsui, Jennifer Gobert, Delphine Desjardins, Jean-François Schohl, Anne Sild, Mari Spratt, Perry Castonguay, Annie De Koninck, Yves Marsh-Armstrong, Nicholas Wiseman, Paul W Ruthazer, Edward S Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
title | Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
title_full | Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
title_fullStr | Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
title_full_unstemmed | Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
title_short | Endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
title_sort | endocannabinoid signaling enhances visual responses through modulation of intracellular chloride levels in retinal ganglion cells |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987138/ https://www.ncbi.nlm.nih.gov/pubmed/27501334 http://dx.doi.org/10.7554/eLife.15932 |
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