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Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling
Astrocytes are critical regulators of neuronal function in the central nervous system (CNS). We have previously shown that astrocytes in the spinal dorsal horn (SDH) have increased intracellular Ca(2+) levels following intraplantar injection of the noxious irritant, formalin. However, the underlying...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108464/ https://www.ncbi.nlm.nih.gov/pubmed/33971918 http://dx.doi.org/10.1186/s13041-021-00788-5 |
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author | Kawanabe, Riku Yoshihara, Kohei Hatada, Izuho Tsuda, Makoto |
author_facet | Kawanabe, Riku Yoshihara, Kohei Hatada, Izuho Tsuda, Makoto |
author_sort | Kawanabe, Riku |
collection | PubMed |
description | Astrocytes are critical regulators of neuronal function in the central nervous system (CNS). We have previously shown that astrocytes in the spinal dorsal horn (SDH) have increased intracellular Ca(2+) levels following intraplantar injection of the noxious irritant, formalin. However, the underlying mechanisms remain unknown. We investigated these mechanisms by focusing on the role of descending noradrenergic (NAergic) signaling because our recent study revealed the essential role of the astrocytic Ca(2+) responses evoked by intraplantar capsaicin. Using in vivo SDH imaging, we found that the Ca(2+) level increase in SDH astrocytes induced by intraplantar formalin injection was suppressed by ablation of SDH-projecting locus coeruleus (LC)-NAergic neurons. Furthermore, the formalin-induced Ca(2+) response was dramatically decreased by the loss of α(1A)-adrenaline receptors (ARs) in astrocytes located in the superficial laminae of the SDH. Moreover, similar inhibition was observed in mice pretreated intrathecally with an α(1A)-AR-specific antagonist. Therefore, activation of α(1A)-ARs via descending LC-NAergic signals may be a common mechanism underlying astrocytic Ca(2+) responses in the SDH evoked by noxious stimuli, including chemical irritants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00788-5. |
format | Online Article Text |
id | pubmed-8108464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81084642021-05-11 Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling Kawanabe, Riku Yoshihara, Kohei Hatada, Izuho Tsuda, Makoto Mol Brain Micro Report Astrocytes are critical regulators of neuronal function in the central nervous system (CNS). We have previously shown that astrocytes in the spinal dorsal horn (SDH) have increased intracellular Ca(2+) levels following intraplantar injection of the noxious irritant, formalin. However, the underlying mechanisms remain unknown. We investigated these mechanisms by focusing on the role of descending noradrenergic (NAergic) signaling because our recent study revealed the essential role of the astrocytic Ca(2+) responses evoked by intraplantar capsaicin. Using in vivo SDH imaging, we found that the Ca(2+) level increase in SDH astrocytes induced by intraplantar formalin injection was suppressed by ablation of SDH-projecting locus coeruleus (LC)-NAergic neurons. Furthermore, the formalin-induced Ca(2+) response was dramatically decreased by the loss of α(1A)-adrenaline receptors (ARs) in astrocytes located in the superficial laminae of the SDH. Moreover, similar inhibition was observed in mice pretreated intrathecally with an α(1A)-AR-specific antagonist. Therefore, activation of α(1A)-ARs via descending LC-NAergic signals may be a common mechanism underlying astrocytic Ca(2+) responses in the SDH evoked by noxious stimuli, including chemical irritants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00788-5. BioMed Central 2021-05-10 /pmc/articles/PMC8108464/ /pubmed/33971918 http://dx.doi.org/10.1186/s13041-021-00788-5 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 | Micro Report Kawanabe, Riku Yoshihara, Kohei Hatada, Izuho Tsuda, Makoto Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
title | Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
title_full | Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
title_fullStr | Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
title_full_unstemmed | Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
title_short | Activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
title_sort | activation of spinal dorsal horn astrocytes by noxious stimuli involves descending noradrenergic signaling |
topic | Micro Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108464/ https://www.ncbi.nlm.nih.gov/pubmed/33971918 http://dx.doi.org/10.1186/s13041-021-00788-5 |
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