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Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis
Treatment of acute pulpitis (AP) is beneficial for pain relief and pulp regeneration. The purinergic P2X7 receptor activation is responsible for the formation and maintenance of inflammation and pain. This study aims to determine the role of the pulp tissue P2X7 receptor to activate the mechanisms o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237923/ https://www.ncbi.nlm.nih.gov/pubmed/35748325 http://dx.doi.org/10.1177/17448069221106844 |
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author | Xiao, Zhi Xu, Min Lan, Lan Xu, Ke Zhang, Yue-Rong |
author_facet | Xiao, Zhi Xu, Min Lan, Lan Xu, Ke Zhang, Yue-Rong |
author_sort | Xiao, Zhi |
collection | PubMed |
description | Treatment of acute pulpitis (AP) is beneficial for pain relief and pulp regeneration. The purinergic P2X7 receptor activation is responsible for the formation and maintenance of inflammation and pain. This study aims to determine the role of the pulp tissue P2X7 receptor to activate the mechanisms of the AP in rats. The Sprague-Dawley rats were divided into groups, namely, normal, normal saline (NS), and lipopolysaccharide (LPS) groups. Alterations in pain behavior were detected through head-withdrawal thresholds (HWTs), and the pathological changes in pulp tissue were studied through hematoxylin and eosin staining. The expression of the P2X7 receptor in pulp tissue was observed through immunohistochemistry and Western Blotting. The effect of the P2X7 receptor antagonist A-740003 on HWTs was also observed. The levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in the pulp tissue of rats were analyzed through enzyme-linked immunosorbent assay. The HWTs were reduced in the rats with AP. Inflammation is formed but was found more severe in the LPS group than the NS group, and the expression levels of the P2X7 receptors in the NS and LPS groups were higher than in the normal group. The periodontal ligament injection of the A-740003 dose-dependant increases the HWTs in rats with AP. The IL-6 and TNF-α levels in the pulp in the NS and LPS groups were increased but reversed by A-740003 injection. In rats with AP, the expression level of the P2X7 receptor and IL-6/TNF-α release was upregulated. The A-740003 can relieve pain and reduce the inflammation progression in rats with AP. |
format | Online Article Text |
id | pubmed-9237923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-92379232022-06-29 Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis Xiao, Zhi Xu, Min Lan, Lan Xu, Ke Zhang, Yue-Rong Mol Pain Research Article Treatment of acute pulpitis (AP) is beneficial for pain relief and pulp regeneration. The purinergic P2X7 receptor activation is responsible for the formation and maintenance of inflammation and pain. This study aims to determine the role of the pulp tissue P2X7 receptor to activate the mechanisms of the AP in rats. The Sprague-Dawley rats were divided into groups, namely, normal, normal saline (NS), and lipopolysaccharide (LPS) groups. Alterations in pain behavior were detected through head-withdrawal thresholds (HWTs), and the pathological changes in pulp tissue were studied through hematoxylin and eosin staining. The expression of the P2X7 receptor in pulp tissue was observed through immunohistochemistry and Western Blotting. The effect of the P2X7 receptor antagonist A-740003 on HWTs was also observed. The levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in the pulp tissue of rats were analyzed through enzyme-linked immunosorbent assay. The HWTs were reduced in the rats with AP. Inflammation is formed but was found more severe in the LPS group than the NS group, and the expression levels of the P2X7 receptors in the NS and LPS groups were higher than in the normal group. The periodontal ligament injection of the A-740003 dose-dependant increases the HWTs in rats with AP. The IL-6 and TNF-α levels in the pulp in the NS and LPS groups were increased but reversed by A-740003 injection. In rats with AP, the expression level of the P2X7 receptor and IL-6/TNF-α release was upregulated. The A-740003 can relieve pain and reduce the inflammation progression in rats with AP. SAGE Publications 2022-06-24 /pmc/articles/PMC9237923/ /pubmed/35748325 http://dx.doi.org/10.1177/17448069221106844 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Xiao, Zhi Xu, Min Lan, Lan Xu, Ke Zhang, Yue-Rong Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
title | Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
title_full | Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
title_fullStr | Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
title_full_unstemmed | Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
title_short | Activation of the P2X7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
title_sort | activation of the p2x7 receptor in the dental pulp tissue contributes to the pain in rats with acute pulpitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237923/ https://www.ncbi.nlm.nih.gov/pubmed/35748325 http://dx.doi.org/10.1177/17448069221106844 |
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