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Systemic effect of mineral aggregate-based cements: histopathological analysis in rats
OBJECTIVE: Several studies reported the local tissue reaction caused by mineral aggregate-based cements. However, few studies have investigated the systemic effects promoted by these cements on liver and kidney when directly applied to connective tissue. The purpose of this in vivo study was to inve...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculdade De Odontologia De Bauru - USP
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701532/ https://www.ncbi.nlm.nih.gov/pubmed/29211283 http://dx.doi.org/10.1590/1678-7757-2016-0634 |
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author | Garcia, Lucas da Fonseca Roberti Huck, Claudia Magalhães, Fernando Augusto Cintra de Souza, Pedro Paulo Chaves de Souza Costa, Carlos Alberto |
author_facet | Garcia, Lucas da Fonseca Roberti Huck, Claudia Magalhães, Fernando Augusto Cintra de Souza, Pedro Paulo Chaves de Souza Costa, Carlos Alberto |
author_sort | Garcia, Lucas da Fonseca Roberti |
collection | PubMed |
description | OBJECTIVE: Several studies reported the local tissue reaction caused by mineral aggregate-based cements. However, few studies have investigated the systemic effects promoted by these cements on liver and kidney when directly applied to connective tissue. The purpose of this in vivo study was to investigate the systemic effect of mineral aggregate-based cements on the livers and kidneys of rats. MATERIAL AND METHODS: Samples of Mineral Trioxide Aggregate (MTA) and a calcium aluminate-based cement (EndoBinder) containing different radiopacifiers were implanted into the dorsum of 40 rats. After 7 and 30 d, samples of subcutaneous, liver and kidney tissues were submitted to histopathological analysis. A score (0-3) was used to grade the inflammatory reaction. Blood samples were collected to evaluate changes in hepatic and renal functions of animals. RESULTS: The moderate inflammatory reaction (2) observed for 7 d in the subcutaneous tissue decreased with time for all cements. The thickness of inflammatory capsules also presented a significant decrease with time (P<.05). Systemically, all cements caused adverse inflammatory reactions in the liver and kidney, being more evident for MTA, persisting until the end of the analysis. Liver functions increased significantly for MTA during 30 d (P<.05). CONCLUSION: The different cements induced to a locally limited inflammatory reaction. However, from the systemic point of view, the cements promoted significant inflammatory reactions in the liver and kidney. For MTA, the reactions were more accentuated. |
format | Online Article Text |
id | pubmed-5701532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Faculdade De Odontologia De Bauru - USP |
record_format | MEDLINE/PubMed |
spelling | pubmed-57015322017-11-30 Systemic effect of mineral aggregate-based cements: histopathological analysis in rats Garcia, Lucas da Fonseca Roberti Huck, Claudia Magalhães, Fernando Augusto Cintra de Souza, Pedro Paulo Chaves de Souza Costa, Carlos Alberto J Appl Oral Sci Original Article OBJECTIVE: Several studies reported the local tissue reaction caused by mineral aggregate-based cements. However, few studies have investigated the systemic effects promoted by these cements on liver and kidney when directly applied to connective tissue. The purpose of this in vivo study was to investigate the systemic effect of mineral aggregate-based cements on the livers and kidneys of rats. MATERIAL AND METHODS: Samples of Mineral Trioxide Aggregate (MTA) and a calcium aluminate-based cement (EndoBinder) containing different radiopacifiers were implanted into the dorsum of 40 rats. After 7 and 30 d, samples of subcutaneous, liver and kidney tissues were submitted to histopathological analysis. A score (0-3) was used to grade the inflammatory reaction. Blood samples were collected to evaluate changes in hepatic and renal functions of animals. RESULTS: The moderate inflammatory reaction (2) observed for 7 d in the subcutaneous tissue decreased with time for all cements. The thickness of inflammatory capsules also presented a significant decrease with time (P<.05). Systemically, all cements caused adverse inflammatory reactions in the liver and kidney, being more evident for MTA, persisting until the end of the analysis. Liver functions increased significantly for MTA during 30 d (P<.05). CONCLUSION: The different cements induced to a locally limited inflammatory reaction. However, from the systemic point of view, the cements promoted significant inflammatory reactions in the liver and kidney. For MTA, the reactions were more accentuated. Faculdade De Odontologia De Bauru - USP 2017 /pmc/articles/PMC5701532/ /pubmed/29211283 http://dx.doi.org/10.1590/1678-7757-2016-0634 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Garcia, Lucas da Fonseca Roberti Huck, Claudia Magalhães, Fernando Augusto Cintra de Souza, Pedro Paulo Chaves de Souza Costa, Carlos Alberto Systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
title | Systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
title_full | Systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
title_fullStr | Systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
title_full_unstemmed | Systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
title_short | Systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
title_sort | systemic effect of mineral aggregate-based cements: histopathological analysis in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701532/ https://www.ncbi.nlm.nih.gov/pubmed/29211283 http://dx.doi.org/10.1590/1678-7757-2016-0634 |
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