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Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization
The objective of this study was to determine whether the use of the most commonly prescribed antibiotics and non-steroidal anti-inflammatory drugs in childhood could disturb enamel mineralization. Forty-two Swiss mice were divided into seven groups: controls; amoxicillin; amoxicillin/clavulanate; er...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841276/ https://www.ncbi.nlm.nih.gov/pubmed/29515175 http://dx.doi.org/10.1038/s41598-018-22607-z |
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author | Serna Muñoz, Clara Pérez Silva, Amparo Solano, Francisco Castells, María Teresa Vicente, Ascensión Ortiz Ruiz, Antonio José |
author_facet | Serna Muñoz, Clara Pérez Silva, Amparo Solano, Francisco Castells, María Teresa Vicente, Ascensión Ortiz Ruiz, Antonio José |
author_sort | Serna Muñoz, Clara |
collection | PubMed |
description | The objective of this study was to determine whether the use of the most commonly prescribed antibiotics and non-steroidal anti-inflammatory drugs in childhood could disturb enamel mineralization. Forty-two Swiss mice were divided into seven groups: controls; amoxicillin; amoxicillin/clavulanate; erythromycin; acetaminophen; ibuprofen and celecoxib, to inhibit cyclooxygenase 2 (COX2). SEM-EDX analysis was conducted on all cusps of the third molars. Calcium (Ca), phosphorus (P), aluminum, potassium, sodium, magnesium and chlorine were quantified. The stoichiometric Ca/P molar ratios were calculated. Immunohistochemical quantification of COX2 in incisors was carried out by image analysis using COX2-specific immunostaining. Groups treated with antibiotics showed no significant differences in the content of the chemical elements. Only acetaminophen and celecoxib showed a significant decrease in Ca and P compared with the control samples. Ca/P ratios showed no difference. Groups treated with amoxicillin, amoxicillin/clavulanate, erythromycin and acetaminophen showed significantly lower amounts of immunoreactive COX2 at the enamel organ maturation stage of the mouse incisors. Our results suggest that COX2 is involved in the maturation stage of the enamel organ and that its inhibition would appear to alter amelogenesis, producing hypomineralization. |
format | Online Article Text |
id | pubmed-5841276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58412762018-03-13 Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization Serna Muñoz, Clara Pérez Silva, Amparo Solano, Francisco Castells, María Teresa Vicente, Ascensión Ortiz Ruiz, Antonio José Sci Rep Article The objective of this study was to determine whether the use of the most commonly prescribed antibiotics and non-steroidal anti-inflammatory drugs in childhood could disturb enamel mineralization. Forty-two Swiss mice were divided into seven groups: controls; amoxicillin; amoxicillin/clavulanate; erythromycin; acetaminophen; ibuprofen and celecoxib, to inhibit cyclooxygenase 2 (COX2). SEM-EDX analysis was conducted on all cusps of the third molars. Calcium (Ca), phosphorus (P), aluminum, potassium, sodium, magnesium and chlorine were quantified. The stoichiometric Ca/P molar ratios were calculated. Immunohistochemical quantification of COX2 in incisors was carried out by image analysis using COX2-specific immunostaining. Groups treated with antibiotics showed no significant differences in the content of the chemical elements. Only acetaminophen and celecoxib showed a significant decrease in Ca and P compared with the control samples. Ca/P ratios showed no difference. Groups treated with amoxicillin, amoxicillin/clavulanate, erythromycin and acetaminophen showed significantly lower amounts of immunoreactive COX2 at the enamel organ maturation stage of the mouse incisors. Our results suggest that COX2 is involved in the maturation stage of the enamel organ and that its inhibition would appear to alter amelogenesis, producing hypomineralization. Nature Publishing Group UK 2018-03-07 /pmc/articles/PMC5841276/ /pubmed/29515175 http://dx.doi.org/10.1038/s41598-018-22607-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Serna Muñoz, Clara Pérez Silva, Amparo Solano, Francisco Castells, María Teresa Vicente, Ascensión Ortiz Ruiz, Antonio José Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization |
title | Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization |
title_full | Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization |
title_fullStr | Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization |
title_full_unstemmed | Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization |
title_short | Effect of antibiotics and NSAIDs on cyclooxygenase-2 in the enamel mineralization |
title_sort | effect of antibiotics and nsaids on cyclooxygenase-2 in the enamel mineralization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841276/ https://www.ncbi.nlm.nih.gov/pubmed/29515175 http://dx.doi.org/10.1038/s41598-018-22607-z |
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