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Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons

Primary afferents are responsible for transmitting signals produced by noxious stimuli from the periphery to the spinal cord. Mu and delta opioid receptors (MOP and DOP) have analgesic properties and are highly expressed in dorsal root ganglia (DRG) neurons. In humans, spinal DOP is almost exclusive...

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Autores principales: Quirion, Béatrice, Beaulieu, Claudie, Côté, Laurie, Parent, Jean‐Luc, Gendron, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543299/
https://www.ncbi.nlm.nih.gov/pubmed/35674691
http://dx.doi.org/10.1111/ejn.15733
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author Quirion, Béatrice
Beaulieu, Claudie
Côté, Laurie
Parent, Jean‐Luc
Gendron, Louis
author_facet Quirion, Béatrice
Beaulieu, Claudie
Côté, Laurie
Parent, Jean‐Luc
Gendron, Louis
author_sort Quirion, Béatrice
collection PubMed
description Primary afferents are responsible for transmitting signals produced by noxious stimuli from the periphery to the spinal cord. Mu and delta opioid receptors (MOP and DOP) have analgesic properties and are highly expressed in dorsal root ganglia (DRG) neurons. In humans, spinal DOP is almost exclusively located on central terminals of DRG neurons, whereas in rodents, it is expressed both on presynaptic terminals and spinal neurons. In this study, we aimed to assess the distribution of MOP and DOP in the DRGs of mice and rats. Using in situ hybridization and immunofluorescence, we visualized MOP and DOP mRNA together with various neuronal markers. In rats and mice, we show that both receptors are expressed, albeit to different extents, in all types of neurons, namely, large and medium myelinated neurons (NF200‐positive), small nonpeptidergic (IB4‐ or P2X3R‐positive) and peptidergic C fibres (Tac1‐positive). Overall, DOP mRNA was found to be mainly expressed in large and medium myelinated neurons, whereas MOP mRNA was mainly found in C fibres. The distribution of MOP and DOP, however, slightly differs between rats and mice, with a higher proportion of small nonpeptidergic C fibres expressing DOP mRNA in mice than in rats. We further found that neither morphine nor inflammation affected the distribution of the receptor mRNA. Because of their location, our results confirm that MOP and DOP have the potential to alleviate similar types of pain and that this effect could slightly differ between species.
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spelling pubmed-95432992022-10-14 Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons Quirion, Béatrice Beaulieu, Claudie Côté, Laurie Parent, Jean‐Luc Gendron, Louis Eur J Neurosci Molecular and Synaptic Mechanisms Primary afferents are responsible for transmitting signals produced by noxious stimuli from the periphery to the spinal cord. Mu and delta opioid receptors (MOP and DOP) have analgesic properties and are highly expressed in dorsal root ganglia (DRG) neurons. In humans, spinal DOP is almost exclusively located on central terminals of DRG neurons, whereas in rodents, it is expressed both on presynaptic terminals and spinal neurons. In this study, we aimed to assess the distribution of MOP and DOP in the DRGs of mice and rats. Using in situ hybridization and immunofluorescence, we visualized MOP and DOP mRNA together with various neuronal markers. In rats and mice, we show that both receptors are expressed, albeit to different extents, in all types of neurons, namely, large and medium myelinated neurons (NF200‐positive), small nonpeptidergic (IB4‐ or P2X3R‐positive) and peptidergic C fibres (Tac1‐positive). Overall, DOP mRNA was found to be mainly expressed in large and medium myelinated neurons, whereas MOP mRNA was mainly found in C fibres. The distribution of MOP and DOP, however, slightly differs between rats and mice, with a higher proportion of small nonpeptidergic C fibres expressing DOP mRNA in mice than in rats. We further found that neither morphine nor inflammation affected the distribution of the receptor mRNA. Because of their location, our results confirm that MOP and DOP have the potential to alleviate similar types of pain and that this effect could slightly differ between species. John Wiley and Sons Inc. 2022-06-14 2022-08 /pmc/articles/PMC9543299/ /pubmed/35674691 http://dx.doi.org/10.1111/ejn.15733 Text en © 2022 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Molecular and Synaptic Mechanisms
Quirion, Béatrice
Beaulieu, Claudie
Côté, Laurie
Parent, Jean‐Luc
Gendron, Louis
Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons
title Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons
title_full Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons
title_fullStr Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons
title_full_unstemmed Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons
title_short Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons
title_sort distribution of delta and mu opioid receptor mrna in rodent dorsal root ganglia neurons
topic Molecular and Synaptic Mechanisms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543299/
https://www.ncbi.nlm.nih.gov/pubmed/35674691
http://dx.doi.org/10.1111/ejn.15733
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