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A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars
Introduction: Recent investigations have attempted to improve regenerative endodontics with the help of stem cell therapy. In vitro studies have shown the ability of different agents to stimulate the differentiation of dental pulp stem cells (DPSC) into odontoblast-like cells. A combination of dexam...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Center for Endodontic Research
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881302/ https://www.ncbi.nlm.nih.gov/pubmed/24396376 |
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author | Moazzami, Fariborz Ghahramani, Yasmin Tamaddon, Ali Mohammad Dehghani Nazhavani, Ali Adl, Alireza |
author_facet | Moazzami, Fariborz Ghahramani, Yasmin Tamaddon, Ali Mohammad Dehghani Nazhavani, Ali Adl, Alireza |
author_sort | Moazzami, Fariborz |
collection | PubMed |
description | Introduction: Recent investigations have attempted to improve regenerative endodontics with the help of stem cell therapy. In vitro studies have shown the ability of different agents to stimulate the differentiation of dental pulp stem cells (DPSC) into odontoblast-like cells. A combination of dexamethasone, β-glycerophosphate and Vitamin D has been proven to induce a successful differentiation. The aim of this animal study was to evaluate the effect of this combination, named odontoblastic differentiating material (ODM), on pulp tissue when used as a capping material. Materials and Methods: Sixty maxillary right and left molars of 30 Sprague-dawley rats were selected for this study. The teeth were exposed under sterile condition. Half of the teeth were capped with mineral trioxide aggregate (MTA) and the other half with ODM. All cavities were restored with glass ionomer. The rats were sacrificed at post-operative intervals of 2 weeks and 2 months. Samples were histologically evaluated for the degree of inflammation and reparative dentin formation. Finally the data was analyzed with Mann-Whitney and Chi-Square tests. Results: Reparative dentin formed in all groups within both time periods and there was no statistically significant difference between the groups in the mentioned time periods. The MTA group, however, showed a statistically significant reduction in inflammation at both time intervals (P<0.05). Compared to MTA, ODM samples showed a greater amount of inflammation in the pulp tissue. Conclusion: ODM, as a pulp capping material, can induce dentinal bridge formation. |
format | Online Article Text |
id | pubmed-3881302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Iranian Center for Endodontic Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-38813022014-01-06 A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars Moazzami, Fariborz Ghahramani, Yasmin Tamaddon, Ali Mohammad Dehghani Nazhavani, Ali Adl, Alireza Iran Endod J Original Article Introduction: Recent investigations have attempted to improve regenerative endodontics with the help of stem cell therapy. In vitro studies have shown the ability of different agents to stimulate the differentiation of dental pulp stem cells (DPSC) into odontoblast-like cells. A combination of dexamethasone, β-glycerophosphate and Vitamin D has been proven to induce a successful differentiation. The aim of this animal study was to evaluate the effect of this combination, named odontoblastic differentiating material (ODM), on pulp tissue when used as a capping material. Materials and Methods: Sixty maxillary right and left molars of 30 Sprague-dawley rats were selected for this study. The teeth were exposed under sterile condition. Half of the teeth were capped with mineral trioxide aggregate (MTA) and the other half with ODM. All cavities were restored with glass ionomer. The rats were sacrificed at post-operative intervals of 2 weeks and 2 months. Samples were histologically evaluated for the degree of inflammation and reparative dentin formation. Finally the data was analyzed with Mann-Whitney and Chi-Square tests. Results: Reparative dentin formed in all groups within both time periods and there was no statistically significant difference between the groups in the mentioned time periods. The MTA group, however, showed a statistically significant reduction in inflammation at both time intervals (P<0.05). Compared to MTA, ODM samples showed a greater amount of inflammation in the pulp tissue. Conclusion: ODM, as a pulp capping material, can induce dentinal bridge formation. Iranian Center for Endodontic Research 2014 2013-12-24 /pmc/articles/PMC3881302/ /pubmed/24396376 Text en © 2014, Iranian Center for Endodontic Research This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Moazzami, Fariborz Ghahramani, Yasmin Tamaddon, Ali Mohammad Dehghani Nazhavani, Ali Adl, Alireza A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars |
title | A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars |
title_full | A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars |
title_fullStr | A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars |
title_full_unstemmed | A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars |
title_short | A Histological Comparison of a New Pulp Capping Material and Mineral Trioxide Aggregate in Rat Molars |
title_sort | histological comparison of a new pulp capping material and mineral trioxide aggregate in rat molars |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881302/ https://www.ncbi.nlm.nih.gov/pubmed/24396376 |
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