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The organisation of spinoparabrachial neurons in the mouse
The anterolateral tract (ALT), which originates from neurons in lamina I and the deep dorsal horn, represents a major ascending output through which nociceptive information is transmitted to brain areas involved in pain perception. Although there is detailed quantitative information concerning the A...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770364/ https://www.ncbi.nlm.nih.gov/pubmed/26101837 http://dx.doi.org/10.1097/j.pain.0000000000000270 |
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author | Cameron, Darren Polgár, Erika Gutierrez-Mecinas, Maria Gomez-Lima, Maria Watanabe, Masahiko Todd, Andrew J. |
author_facet | Cameron, Darren Polgár, Erika Gutierrez-Mecinas, Maria Gomez-Lima, Maria Watanabe, Masahiko Todd, Andrew J. |
author_sort | Cameron, Darren |
collection | PubMed |
description | The anterolateral tract (ALT), which originates from neurons in lamina I and the deep dorsal horn, represents a major ascending output through which nociceptive information is transmitted to brain areas involved in pain perception. Although there is detailed quantitative information concerning the ALT in the rat, much less is known about this system in the mouse, which is increasingly being used for studies of spinal pain mechanisms because of the availability of genetically modified lines. The aim of this study was therefore to determine the extent to which information about the ALT in the rat can be extrapolated to the mouse. Our results suggest that as in the rat, most lamina I ALT projection neurons in the lumbar enlargement can be retrogradely labelled from the lateral parabrachial area, that the majority of these cells (∼90%) express the neurokinin 1 receptor (NK1r), and that these are larger than other NK1r-expressing neurons in this lamina. This means that many lamina I spinoparabrachial cells can be identified in NK1r-immunostained sections from animals that have not received retrograde tracer injections. However, we also observed certain species differences, in particular we found that many spinoparabrachial cells in laminae III and IV lack the NK1r, meaning that they cannot be identified based solely on the expression of this receptor. We also provide evidence that the majority of spinoparabrachial cells are glutamatergic and that some express substance P. These findings will be important for studies designed to unravel the complex neuronal circuitry that underlies spinal pain processing. |
format | Online Article Text |
id | pubmed-4770364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-47703642016-03-19 The organisation of spinoparabrachial neurons in the mouse Cameron, Darren Polgár, Erika Gutierrez-Mecinas, Maria Gomez-Lima, Maria Watanabe, Masahiko Todd, Andrew J. Pain Research Paper The anterolateral tract (ALT), which originates from neurons in lamina I and the deep dorsal horn, represents a major ascending output through which nociceptive information is transmitted to brain areas involved in pain perception. Although there is detailed quantitative information concerning the ALT in the rat, much less is known about this system in the mouse, which is increasingly being used for studies of spinal pain mechanisms because of the availability of genetically modified lines. The aim of this study was therefore to determine the extent to which information about the ALT in the rat can be extrapolated to the mouse. Our results suggest that as in the rat, most lamina I ALT projection neurons in the lumbar enlargement can be retrogradely labelled from the lateral parabrachial area, that the majority of these cells (∼90%) express the neurokinin 1 receptor (NK1r), and that these are larger than other NK1r-expressing neurons in this lamina. This means that many lamina I spinoparabrachial cells can be identified in NK1r-immunostained sections from animals that have not received retrograde tracer injections. However, we also observed certain species differences, in particular we found that many spinoparabrachial cells in laminae III and IV lack the NK1r, meaning that they cannot be identified based solely on the expression of this receptor. We also provide evidence that the majority of spinoparabrachial cells are glutamatergic and that some express substance P. These findings will be important for studies designed to unravel the complex neuronal circuitry that underlies spinal pain processing. Wolters Kluwer 2015-06-22 2015-10 /pmc/articles/PMC4770364/ /pubmed/26101837 http://dx.doi.org/10.1097/j.pain.0000000000000270 Text en © 2015 International Association for the Study of Pain This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Cameron, Darren Polgár, Erika Gutierrez-Mecinas, Maria Gomez-Lima, Maria Watanabe, Masahiko Todd, Andrew J. The organisation of spinoparabrachial neurons in the mouse |
title | The organisation of spinoparabrachial neurons in the mouse |
title_full | The organisation of spinoparabrachial neurons in the mouse |
title_fullStr | The organisation of spinoparabrachial neurons in the mouse |
title_full_unstemmed | The organisation of spinoparabrachial neurons in the mouse |
title_short | The organisation of spinoparabrachial neurons in the mouse |
title_sort | organisation of spinoparabrachial neurons in the mouse |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770364/ https://www.ncbi.nlm.nih.gov/pubmed/26101837 http://dx.doi.org/10.1097/j.pain.0000000000000270 |
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