Cargando…

Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds

BACKGROUND: A small proportion of lamina I neurons of the spinal cord project upon the hindbrain and are thought to engage descending pathways that modulate the behavioural response to peripheral injury. Early postnatal development of nociception in rats is associated with exaggerated and diffuse cu...

Descripción completa

Detalles Bibliográficos
Autores principales: Man, Sharon HW, Géranton, Sandrine M, Hunt, Stephen P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528436/
https://www.ncbi.nlm.nih.gov/pubmed/22540287
http://dx.doi.org/10.1186/1744-8069-8-35
_version_ 1782253824824573952
author Man, Sharon HW
Géranton, Sandrine M
Hunt, Stephen P
author_facet Man, Sharon HW
Géranton, Sandrine M
Hunt, Stephen P
author_sort Man, Sharon HW
collection PubMed
description BACKGROUND: A small proportion of lamina I neurons of the spinal cord project upon the hindbrain and are thought to engage descending pathways that modulate the behavioural response to peripheral injury. Early postnatal development of nociception in rats is associated with exaggerated and diffuse cutaneous reflexes with a gradual refinement of responses over the first postnatal weeks related to increased participation of inhibitory networks. This study examined the postnatal development of lamina I projection neurons from postnatal day 3 (P3) until P48. RESULTS: At P3, a subset of lamina I neurons were found to express the neurokinin 1 (NK1) receptor. Using fluorogold retrograde tracing, we found that the NK1 positive neurons projected upon the parabrachial nucleus (PB) within the hindbrain. Using c-fos immunohistochemistry, we showed that lamina I and PB neurons in P3 rats responded to noxious stimulation of the periphery. Finally, ablation of lamina I neurons with substance-P saporin conjugates at P3 resulted in increased mechanical sensitivity from P45 onwards compared to control animals of the same age. CONCLUSIONS: These results suggest that the lamina I pathway is present and functional at least from P3 and required for establishing and fine-tuning mechanical sensitivity in adult rats.
format Online
Article
Text
id pubmed-3528436
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-35284362013-01-03 Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds Man, Sharon HW Géranton, Sandrine M Hunt, Stephen P Mol Pain Research BACKGROUND: A small proportion of lamina I neurons of the spinal cord project upon the hindbrain and are thought to engage descending pathways that modulate the behavioural response to peripheral injury. Early postnatal development of nociception in rats is associated with exaggerated and diffuse cutaneous reflexes with a gradual refinement of responses over the first postnatal weeks related to increased participation of inhibitory networks. This study examined the postnatal development of lamina I projection neurons from postnatal day 3 (P3) until P48. RESULTS: At P3, a subset of lamina I neurons were found to express the neurokinin 1 (NK1) receptor. Using fluorogold retrograde tracing, we found that the NK1 positive neurons projected upon the parabrachial nucleus (PB) within the hindbrain. Using c-fos immunohistochemistry, we showed that lamina I and PB neurons in P3 rats responded to noxious stimulation of the periphery. Finally, ablation of lamina I neurons with substance-P saporin conjugates at P3 resulted in increased mechanical sensitivity from P45 onwards compared to control animals of the same age. CONCLUSIONS: These results suggest that the lamina I pathway is present and functional at least from P3 and required for establishing and fine-tuning mechanical sensitivity in adult rats. BioMed Central 2012-04-27 /pmc/articles/PMC3528436/ /pubmed/22540287 http://dx.doi.org/10.1186/1744-8069-8-35 Text en Copyright ©2012 Man et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Man, Sharon HW
Géranton, Sandrine M
Hunt, Stephen P
Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
title Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
title_full Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
title_fullStr Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
title_full_unstemmed Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
title_short Lamina I NK1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
title_sort lamina i nk1 expressing projection neurones are functional in early postnatal rats and contribute to the setting up of adult mechanical sensory thresholds
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528436/
https://www.ncbi.nlm.nih.gov/pubmed/22540287
http://dx.doi.org/10.1186/1744-8069-8-35
work_keys_str_mv AT mansharonhw laminaink1expressingprojectionneuronesarefunctionalinearlypostnatalratsandcontributetothesettingupofadultmechanicalsensorythresholds
AT gerantonsandrinem laminaink1expressingprojectionneuronesarefunctionalinearlypostnatalratsandcontributetothesettingupofadultmechanicalsensorythresholds
AT huntstephenp laminaink1expressingprojectionneuronesarefunctionalinearlypostnatalratsandcontributetothesettingupofadultmechanicalsensorythresholds