Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.jobcr.2018.10.004 http://hdl.handle.net/11449/228604 |
Resumo: | The most important microscopic characteristic of Cyclosporine A-induced gingival overgrowth is fibroepithelial hyperplasia. Objective: The objective was to investigate the influence of previous exposure to Cyclosporine A over gingival epithelium in experimental periodontitis in rats. Methods: Twenty Wistar rats with 12 weeks-old were divided into four groups with 5 animals each: Control Group (CG); Cyclosporine Group (CsAG); Ligature group (LG) and Cyclosporine and Ligature Group (CsALG). Daily doses of CsA (10 mg/kg) were applied to CsAG and CsALG during 60 days since the beginning of the experiment and, a ligature was placed in LG and CsALG 30 days after the beginning of the experiment. After 60 days, animals were euthanized and gingival tissue was processed to histomorphometric analysis of epithelial thickness (mm2), immunohistochemical expression of PCNA (%) and inflammatory response. Data were analyzed by Kruskal-Wallis and Mann Whitney at 0.05 significance level. Results: Considering epithelial thickness, CG was thinner than all groups, CsALG was the largest and CsAG and LG were similar between each other. Regarding the PCNA expression CG (16.46 ± 9.26) was similar to CsAG (34.47 ± 19.75) and, LG (59.02 ± 10.33) was similar to CsALG (40.59 ± 18.25). Significant difference (p < 0.05) occurred only in inflammation presence comparing CG/LG and CsAG/CsALG. A weak positive correlation between the number of PCNA+ and inflammatory cells (p = 0.001; r = 0.611) was observed. Conclusion: Based on these results it was concluded that the enlargement of gingival epithelium observed in experimental periodontitis can be increased by previous exposition to CsA and inflammatory conditions enhanced proliferative activity of the keratinocytes. |
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Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitisCyclosporine AEpithelial hyperplasiaGingival overgrowthImmunohistochemical analysisInflammationPCNAProliferative indexThe most important microscopic characteristic of Cyclosporine A-induced gingival overgrowth is fibroepithelial hyperplasia. Objective: The objective was to investigate the influence of previous exposure to Cyclosporine A over gingival epithelium in experimental periodontitis in rats. Methods: Twenty Wistar rats with 12 weeks-old were divided into four groups with 5 animals each: Control Group (CG); Cyclosporine Group (CsAG); Ligature group (LG) and Cyclosporine and Ligature Group (CsALG). Daily doses of CsA (10 mg/kg) were applied to CsAG and CsALG during 60 days since the beginning of the experiment and, a ligature was placed in LG and CsALG 30 days after the beginning of the experiment. After 60 days, animals were euthanized and gingival tissue was processed to histomorphometric analysis of epithelial thickness (mm2), immunohistochemical expression of PCNA (%) and inflammatory response. Data were analyzed by Kruskal-Wallis and Mann Whitney at 0.05 significance level. Results: Considering epithelial thickness, CG was thinner than all groups, CsALG was the largest and CsAG and LG were similar between each other. Regarding the PCNA expression CG (16.46 ± 9.26) was similar to CsAG (34.47 ± 19.75) and, LG (59.02 ± 10.33) was similar to CsALG (40.59 ± 18.25). Significant difference (p < 0.05) occurred only in inflammation presence comparing CG/LG and CsAG/CsALG. A weak positive correlation between the number of PCNA+ and inflammatory cells (p = 0.001; r = 0.611) was observed. Conclusion: Based on these results it was concluded that the enlargement of gingival epithelium observed in experimental periodontitis can be increased by previous exposition to CsA and inflammatory conditions enhanced proliferative activity of the keratinocytes.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Periodontics Department Department of Dentistry of Universiy of TaubatéDepartament of Oral Biopathology of Institute of Science and Tecnology São Paulo State University, São José Dos CamposUNISA - Santo Amaro UniversityDepartament of Oral Biopathology of Institute of Science and Tecnology São Paulo State University, São José Dos CamposFAPESP: 08/54784-4Periodontics DepartmentUniversidade Estadual Paulista (UNESP)UNISA - Santo Amaro UniversityRicardo, Lucilene Hernandesdo Prado, Renata Falchete [UNESP]Carvalho, Yasmin Rodarte [UNESP]da Silva Peralta, FelipePallos, Debora2022-04-29T08:27:45Z2022-04-29T08:27:45Z2019-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article86-90http://dx.doi.org/10.1016/j.jobcr.2018.10.004Journal of Oral Biology and Craniofacial Research, v. 9, n. 1, p. 86-90, 2019.2212-4268http://hdl.handle.net/11449/22860410.1016/j.jobcr.2018.10.0042-s2.0-85055334491Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Oral Biology and Craniofacial Researchinfo:eu-repo/semantics/openAccess2022-04-29T08:27:45Zoai:repositorio.unesp.br:11449/228604Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:34:40.542545Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
title |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
spellingShingle |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis Ricardo, Lucilene Hernandes Cyclosporine A Epithelial hyperplasia Gingival overgrowth Immunohistochemical analysis Inflammation PCNA Proliferative index |
title_short |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
title_full |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
title_fullStr |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
title_full_unstemmed |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
title_sort |
Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis |
author |
Ricardo, Lucilene Hernandes |
author_facet |
Ricardo, Lucilene Hernandes do Prado, Renata Falchete [UNESP] Carvalho, Yasmin Rodarte [UNESP] da Silva Peralta, Felipe Pallos, Debora |
author_role |
author |
author2 |
do Prado, Renata Falchete [UNESP] Carvalho, Yasmin Rodarte [UNESP] da Silva Peralta, Felipe Pallos, Debora |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Periodontics Department Universidade Estadual Paulista (UNESP) UNISA - Santo Amaro University |
dc.contributor.author.fl_str_mv |
Ricardo, Lucilene Hernandes do Prado, Renata Falchete [UNESP] Carvalho, Yasmin Rodarte [UNESP] da Silva Peralta, Felipe Pallos, Debora |
dc.subject.por.fl_str_mv |
Cyclosporine A Epithelial hyperplasia Gingival overgrowth Immunohistochemical analysis Inflammation PCNA Proliferative index |
topic |
Cyclosporine A Epithelial hyperplasia Gingival overgrowth Immunohistochemical analysis Inflammation PCNA Proliferative index |
description |
The most important microscopic characteristic of Cyclosporine A-induced gingival overgrowth is fibroepithelial hyperplasia. Objective: The objective was to investigate the influence of previous exposure to Cyclosporine A over gingival epithelium in experimental periodontitis in rats. Methods: Twenty Wistar rats with 12 weeks-old were divided into four groups with 5 animals each: Control Group (CG); Cyclosporine Group (CsAG); Ligature group (LG) and Cyclosporine and Ligature Group (CsALG). Daily doses of CsA (10 mg/kg) were applied to CsAG and CsALG during 60 days since the beginning of the experiment and, a ligature was placed in LG and CsALG 30 days after the beginning of the experiment. After 60 days, animals were euthanized and gingival tissue was processed to histomorphometric analysis of epithelial thickness (mm2), immunohistochemical expression of PCNA (%) and inflammatory response. Data were analyzed by Kruskal-Wallis and Mann Whitney at 0.05 significance level. Results: Considering epithelial thickness, CG was thinner than all groups, CsALG was the largest and CsAG and LG were similar between each other. Regarding the PCNA expression CG (16.46 ± 9.26) was similar to CsAG (34.47 ± 19.75) and, LG (59.02 ± 10.33) was similar to CsALG (40.59 ± 18.25). Significant difference (p < 0.05) occurred only in inflammation presence comparing CG/LG and CsAG/CsALG. A weak positive correlation between the number of PCNA+ and inflammatory cells (p = 0.001; r = 0.611) was observed. Conclusion: Based on these results it was concluded that the enlargement of gingival epithelium observed in experimental periodontitis can be increased by previous exposition to CsA and inflammatory conditions enhanced proliferative activity of the keratinocytes. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-01-01 2022-04-29T08:27:45Z 2022-04-29T08:27:45Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.jobcr.2018.10.004 Journal of Oral Biology and Craniofacial Research, v. 9, n. 1, p. 86-90, 2019. 2212-4268 http://hdl.handle.net/11449/228604 10.1016/j.jobcr.2018.10.004 2-s2.0-85055334491 |
url |
http://dx.doi.org/10.1016/j.jobcr.2018.10.004 http://hdl.handle.net/11449/228604 |
identifier_str_mv |
Journal of Oral Biology and Craniofacial Research, v. 9, n. 1, p. 86-90, 2019. 2212-4268 10.1016/j.jobcr.2018.10.004 2-s2.0-85055334491 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Oral Biology and Craniofacial Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
86-90 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1808129440177192960 |