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Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice

We had recently reported that linalool odor exposure induced significant analgesic effects in mice and that the effects were disappeared in olfactory-deprived mice in which the olfactory epithelium was damaged, thus indicating that the effects were triggered by chemical senses evoked by linalool odo...

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Autores principales: Kashiwadani, Hideki, Higa, Yurina, Sugimura, Mitsutaka, Kuwaki, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077846/
https://www.ncbi.nlm.nih.gov/pubmed/33902628
http://dx.doi.org/10.1186/s12993-021-00176-y
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author Kashiwadani, Hideki
Higa, Yurina
Sugimura, Mitsutaka
Kuwaki, Tomoyuki
author_facet Kashiwadani, Hideki
Higa, Yurina
Sugimura, Mitsutaka
Kuwaki, Tomoyuki
author_sort Kashiwadani, Hideki
collection PubMed
description We had recently reported that linalool odor exposure induced significant analgesic effects in mice and that the effects were disappeared in olfactory-deprived mice in which the olfactory epithelium was damaged, thus indicating that the effects were triggered by chemical senses evoked by linalool odor exposure. However, the peripheral neuronal mechanisms, including linalool receptors that contribute toward triggering the linalool odor-induced analgesia, still remain unexplored. In vitro studies have shown that the transient receptor potential ankyrin 1 (TRPA1) responded to linalool, thus raising the possibility that TRPA1 expressed on the trigeminal nerve terminal detects linalool odor inhaled into the nostril and triggers the analgesic effects. To address this hypothesis, we measured the behavioral pain threshold for noxious mechanical stimulation in TRPA1-deficient mice. In contrast to our expectation, we found a significant increase in the threshold after linalool odor exposure in TRPA1-deficient mice, indicating the analgesic effects of linalool odor even in TRPA1-deficient mice. Furthermore, intranasal application of TRPA1 selective antagonist did not alter the analgesic effect of linalool odor. These results showed that the linalool odor-induced analgesia was triggered by a TRPA1-independent pathway in mice.
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spelling pubmed-80778462021-04-29 Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice Kashiwadani, Hideki Higa, Yurina Sugimura, Mitsutaka Kuwaki, Tomoyuki Behav Brain Funct Short Paper We had recently reported that linalool odor exposure induced significant analgesic effects in mice and that the effects were disappeared in olfactory-deprived mice in which the olfactory epithelium was damaged, thus indicating that the effects were triggered by chemical senses evoked by linalool odor exposure. However, the peripheral neuronal mechanisms, including linalool receptors that contribute toward triggering the linalool odor-induced analgesia, still remain unexplored. In vitro studies have shown that the transient receptor potential ankyrin 1 (TRPA1) responded to linalool, thus raising the possibility that TRPA1 expressed on the trigeminal nerve terminal detects linalool odor inhaled into the nostril and triggers the analgesic effects. To address this hypothesis, we measured the behavioral pain threshold for noxious mechanical stimulation in TRPA1-deficient mice. In contrast to our expectation, we found a significant increase in the threshold after linalool odor exposure in TRPA1-deficient mice, indicating the analgesic effects of linalool odor even in TRPA1-deficient mice. Furthermore, intranasal application of TRPA1 selective antagonist did not alter the analgesic effect of linalool odor. These results showed that the linalool odor-induced analgesia was triggered by a TRPA1-independent pathway in mice. BioMed Central 2021-04-26 /pmc/articles/PMC8077846/ /pubmed/33902628 http://dx.doi.org/10.1186/s12993-021-00176-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Paper
Kashiwadani, Hideki
Higa, Yurina
Sugimura, Mitsutaka
Kuwaki, Tomoyuki
Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice
title Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice
title_full Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice
title_fullStr Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice
title_full_unstemmed Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice
title_short Linalool odor‐induced analgesia is triggered by TRPA1-independent pathway in mice
title_sort linalool odor‐induced analgesia is triggered by trpa1-independent pathway in mice
topic Short Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077846/
https://www.ncbi.nlm.nih.gov/pubmed/33902628
http://dx.doi.org/10.1186/s12993-021-00176-y
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