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Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions

Infection-induced chronic pain is an under-studied pain condition. One example is apical periodontitis, which evokes considerable mechanical allodynia that persists after treatment in 7% to 12% of patients. Available analgesics often provide incomplete relief. However, a preclinical model to study p...

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Autores principales: Mohaved, Saeed B, Shilpa, Ganatra, Li, Qun, Austah, Obadah, Bendele, Michelle, Brock, Robert, Ruparel, Nikita B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977224/
https://www.ncbi.nlm.nih.gov/pubmed/31902318
http://dx.doi.org/10.1177/1744806919900725
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author Mohaved, Saeed B
Shilpa, Ganatra
Li, Qun
Austah, Obadah
Bendele, Michelle
Brock, Robert
Ruparel, Nikita B
author_facet Mohaved, Saeed B
Shilpa, Ganatra
Li, Qun
Austah, Obadah
Bendele, Michelle
Brock, Robert
Ruparel, Nikita B
author_sort Mohaved, Saeed B
collection PubMed
description Infection-induced chronic pain is an under-studied pain condition. One example is apical periodontitis, which evokes considerable mechanical allodynia that persists after treatment in 7% to 12% of patients. Available analgesics often provide incomplete relief. However, a preclinical model to study pain mechanisms associated with apical periodontitis is not available. Here, we report a mouse model of apical periodontitis to facilitate studies determining mechanisms mediating persistent infection-induced pain. Mice were anesthetized and the left first molar was exposed to the oral environment for six weeks. Bone resorption, as an indicator of apical periodontitis, was quantified using microcomputed tomography. Mechanical allodynia was determined using extraoral von-Frey filaments in both male and female mice. The expression of c-fos in the medullary dorsal horn was assessed using immunohistochemistry. Mice with apical periodontitis developed significant mechanical allodynia by day 7 that was maintained for 42 days. Mechanical thresholds were significantly lower in females compared to males. Administration of ibuprofen, morphine, or MK-801 reversed mechanical allodynia. Finally, apical periodontitis triggered an upregulation of c-fos in the medullary dorsal horn. Collectively, this model simulates signs of clinical pain experienced by patients with apical periodontitis, detects sex differences in allodynia, and permits the study of peripheral and central trigeminal pain mechanisms.
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spelling pubmed-69772242020-02-06 Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions Mohaved, Saeed B Shilpa, Ganatra Li, Qun Austah, Obadah Bendele, Michelle Brock, Robert Ruparel, Nikita B Mol Pain Methodology Infection-induced chronic pain is an under-studied pain condition. One example is apical periodontitis, which evokes considerable mechanical allodynia that persists after treatment in 7% to 12% of patients. Available analgesics often provide incomplete relief. However, a preclinical model to study pain mechanisms associated with apical periodontitis is not available. Here, we report a mouse model of apical periodontitis to facilitate studies determining mechanisms mediating persistent infection-induced pain. Mice were anesthetized and the left first molar was exposed to the oral environment for six weeks. Bone resorption, as an indicator of apical periodontitis, was quantified using microcomputed tomography. Mechanical allodynia was determined using extraoral von-Frey filaments in both male and female mice. The expression of c-fos in the medullary dorsal horn was assessed using immunohistochemistry. Mice with apical periodontitis developed significant mechanical allodynia by day 7 that was maintained for 42 days. Mechanical thresholds were significantly lower in females compared to males. Administration of ibuprofen, morphine, or MK-801 reversed mechanical allodynia. Finally, apical periodontitis triggered an upregulation of c-fos in the medullary dorsal horn. Collectively, this model simulates signs of clinical pain experienced by patients with apical periodontitis, detects sex differences in allodynia, and permits the study of peripheral and central trigeminal pain mechanisms. SAGE Publications 2020-01-21 /pmc/articles/PMC6977224/ /pubmed/31902318 http://dx.doi.org/10.1177/1744806919900725 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: 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 Methodology
Mohaved, Saeed B
Shilpa, Ganatra
Li, Qun
Austah, Obadah
Bendele, Michelle
Brock, Robert
Ruparel, Nikita B
Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions
title Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions
title_full Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions
title_fullStr Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions
title_full_unstemmed Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions
title_short Apical periodontitis-induced mechanical allodynia: A mouse model to study infection-induced chronic pain conditions
title_sort apical periodontitis-induced mechanical allodynia: a mouse model to study infection-induced chronic pain conditions
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977224/
https://www.ncbi.nlm.nih.gov/pubmed/31902318
http://dx.doi.org/10.1177/1744806919900725
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