Cyclosporine A – Induced gingival overgrowth and proliferating cell nuclear antigen expression in experimental periodontitis

Detalhes bibliográficos
Autor(a) principal: Ricardo, Lucilene Hernandes
Data de Publicação: 2019
Outros Autores: do Prado, Renata Falchete [UNESP], Carvalho, Yasmin Rodarte [UNESP], da Silva Peralta, Felipe, Pallos, Debora
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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spelling 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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