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Autonomic fiber sprouting in the skin in chronic inflammation

Pain is a major symptom associated with chronic inflammation. In previous work from our laboratory, we have shown that in animal models of neuropathic pain there is a sprouting of sympathetic fibers into the upper dermis, a territory normally devoid of them. However, it is not known whether such sym...

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Autores principales: Almarestani, Lina, Longo, Geraldine, Ribeiro-da-Silva, Alfredo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637239/
https://www.ncbi.nlm.nih.gov/pubmed/19014600
http://dx.doi.org/10.1186/1744-8069-4-56
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author Almarestani, Lina
Longo, Geraldine
Ribeiro-da-Silva, Alfredo
author_facet Almarestani, Lina
Longo, Geraldine
Ribeiro-da-Silva, Alfredo
author_sort Almarestani, Lina
collection PubMed
description Pain is a major symptom associated with chronic inflammation. In previous work from our laboratory, we have shown that in animal models of neuropathic pain there is a sprouting of sympathetic fibers into the upper dermis, a territory normally devoid of them. However, it is not known whether such sympathetic spouting, which is likely trophic factor mediated, also occurs in chronic inflammation and arthritis. In the present study, we used a rat model of chronic inflammation in which a small single dose of complete Freund's adjuvant (CFA) was injected subcutaneously, unilaterally, into the plantar surface of the hindpaw. This led to a localized long-term skin inflammation and arthritis in all joints of the hindpaw. Animals were perfused with histological fixatives at 1, 2, 3 or 4 weeks after the injection. Experimental animals treated with CFA were compared to saline-injected animals. We then investigated the changes in the pattern of peripheral innervation of the peptidergic nociceptors and sympathetic fibers in rat glabrous hindpaw skin. Antibodies directed towards calcitonin gene-related peptide (CGRP) and dopamine beta-hydroxylase (DBH) were used for the staining of peptidergic and sympathetic fibers, respectively. Immunofluorescence was then used to analyze the different nerve fiber populations of the upper dermis. At 4 weeks following CFA treatment, DBH-immunoreactive (IR) fibers were found to sprout into the upper dermis, in a pattern similar to the one we had observed in animals with a chronic constriction injury of the sciatic nerve in a previous publication. There was also a significant increase in the density of CGRP-IR fibers in the upper dermis in CFA treated animals at 2, 3 and 4 weeks post-injection. The increased peptidergic fiber innervation and the ectopic autonomic fibers found in the upper dermis may have a role in the pain-related behavior displayed by these animals.
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spelling pubmed-26372392009-02-07 Autonomic fiber sprouting in the skin in chronic inflammation Almarestani, Lina Longo, Geraldine Ribeiro-da-Silva, Alfredo Mol Pain Short Report Pain is a major symptom associated with chronic inflammation. In previous work from our laboratory, we have shown that in animal models of neuropathic pain there is a sprouting of sympathetic fibers into the upper dermis, a territory normally devoid of them. However, it is not known whether such sympathetic spouting, which is likely trophic factor mediated, also occurs in chronic inflammation and arthritis. In the present study, we used a rat model of chronic inflammation in which a small single dose of complete Freund's adjuvant (CFA) was injected subcutaneously, unilaterally, into the plantar surface of the hindpaw. This led to a localized long-term skin inflammation and arthritis in all joints of the hindpaw. Animals were perfused with histological fixatives at 1, 2, 3 or 4 weeks after the injection. Experimental animals treated with CFA were compared to saline-injected animals. We then investigated the changes in the pattern of peripheral innervation of the peptidergic nociceptors and sympathetic fibers in rat glabrous hindpaw skin. Antibodies directed towards calcitonin gene-related peptide (CGRP) and dopamine beta-hydroxylase (DBH) were used for the staining of peptidergic and sympathetic fibers, respectively. Immunofluorescence was then used to analyze the different nerve fiber populations of the upper dermis. At 4 weeks following CFA treatment, DBH-immunoreactive (IR) fibers were found to sprout into the upper dermis, in a pattern similar to the one we had observed in animals with a chronic constriction injury of the sciatic nerve in a previous publication. There was also a significant increase in the density of CGRP-IR fibers in the upper dermis in CFA treated animals at 2, 3 and 4 weeks post-injection. The increased peptidergic fiber innervation and the ectopic autonomic fibers found in the upper dermis may have a role in the pain-related behavior displayed by these animals. BioMed Central 2008-11-14 /pmc/articles/PMC2637239/ /pubmed/19014600 http://dx.doi.org/10.1186/1744-8069-4-56 Text en Copyright © 2008 Almarestani 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 Short Report
Almarestani, Lina
Longo, Geraldine
Ribeiro-da-Silva, Alfredo
Autonomic fiber sprouting in the skin in chronic inflammation
title Autonomic fiber sprouting in the skin in chronic inflammation
title_full Autonomic fiber sprouting in the skin in chronic inflammation
title_fullStr Autonomic fiber sprouting in the skin in chronic inflammation
title_full_unstemmed Autonomic fiber sprouting in the skin in chronic inflammation
title_short Autonomic fiber sprouting in the skin in chronic inflammation
title_sort autonomic fiber sprouting in the skin in chronic inflammation
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637239/
https://www.ncbi.nlm.nih.gov/pubmed/19014600
http://dx.doi.org/10.1186/1744-8069-4-56
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