In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts

Detalhes bibliográficos
Autor(a) principal: Basso, Fernanda G.
Data de Publicação: 2012
Outros Autores: Pansani, Taisa N. [UNESP], Turrioni, Ana Paula S. [UNESP], Bagnato, Vanderlei S., Hebling, Josimeri [UNESP], De Souza Costa, Carlos A. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1155/2012/719452
http://hdl.handle.net/11449/73492
Resumo: The aim of this study was to determine adequate energy doses using specific parameters of LLLT to produce biostimulatory effects on human gingival fibroblast culture. Cells (3 10 4 cells/cm 2) were seeded on 24-well acrylic plates using plain DMEM supplemented with 10 fetal bovine serum. After 48-hour incubation with 5 CO2 at 37C, cells were irradiated with a InGaAsP diode laser prototype (LASERTable; 780 3 nm; 40mW) with energy doses of 0.5, 1.5, 3, 5, and 7J/cm 2. Cells were irradiated every 24h totalizing 3 applications. Twenty-four hours after the last irradiation, cell metabolism was evaluated by the MTT assay and the two most effective doses (0.5 and 3J/cm 2) were selected to evaluate the cell number (trypan blue assay) and the cell migration capacity (wound healing assay; transwell migration assay). Data were analyzed by the Kruskal-Wallis and Mann-Whitney nonparametric tests with statistical significance of 5. Irradiation of the fibroblasts with 0.5 and 3J/cm 2 resulted in significant increase in cell metabolism compared with the nonrradiated group (P 0.05). Both energy doses promoted significant increase in the cell number as well as in cell migration (P 0.05). These results demonstrate that, under the tested conditions, LLLT promoted biostimulation of fibroblasts in vitro. Copyright © 2012 Fernanda G. Basso et al.
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spelling In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblastsThe aim of this study was to determine adequate energy doses using specific parameters of LLLT to produce biostimulatory effects on human gingival fibroblast culture. Cells (3 10 4 cells/cm 2) were seeded on 24-well acrylic plates using plain DMEM supplemented with 10 fetal bovine serum. After 48-hour incubation with 5 CO2 at 37C, cells were irradiated with a InGaAsP diode laser prototype (LASERTable; 780 3 nm; 40mW) with energy doses of 0.5, 1.5, 3, 5, and 7J/cm 2. Cells were irradiated every 24h totalizing 3 applications. Twenty-four hours after the last irradiation, cell metabolism was evaluated by the MTT assay and the two most effective doses (0.5 and 3J/cm 2) were selected to evaluate the cell number (trypan blue assay) and the cell migration capacity (wound healing assay; transwell migration assay). Data were analyzed by the Kruskal-Wallis and Mann-Whitney nonparametric tests with statistical significance of 5. Irradiation of the fibroblasts with 0.5 and 3J/cm 2 resulted in significant increase in cell metabolism compared with the nonrradiated group (P 0.05). Both energy doses promoted significant increase in the cell number as well as in cell migration (P 0.05). These results demonstrate that, under the tested conditions, LLLT promoted biostimulation of fibroblasts in vitro. Copyright © 2012 Fernanda G. Basso et al.Faculdade de Odontologia de Piracicaba Universidade Estadual de Campinas (UNICAMP), 13414-903 Piracicaba SPFaculdade de Odontologia de Araraquara Universidade de Estadual Paulista (UNESP), 14801-903 Araraquara, SPInstituto de Fsica de so Carlos Universidade de São Paulo (USP), 13560-970 São Carlos, SPDepartamento de Fisiologia e Patologia Faculdade de Odontologia de Araraquara Universidade Estadual Paulista, Rua Humait 1680, Centro Caixa Postal: 331, 14801903 Araraquara SPFaculdade de Odontologia de Araraquara Universidade de Estadual Paulista (UNESP), 14801-903 Araraquara, SPDepartamento de Fisiologia e Patologia Faculdade de Odontologia de Araraquara Universidade Estadual Paulista, Rua Humait 1680, Centro Caixa Postal: 331, 14801903 Araraquara SPUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Basso, Fernanda G.Pansani, Taisa N. [UNESP]Turrioni, Ana Paula S. [UNESP]Bagnato, Vanderlei S.Hebling, Josimeri [UNESP]De Souza Costa, Carlos A. [UNESP]2014-05-27T11:26:56Z2014-05-27T11:26:56Z2012-08-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1155/2012/719452International Journal of Dentistry.1687-87281687-8736http://hdl.handle.net/11449/7349210.1155/2012/7194522-s2.0-848649599752-s2.0-84864959975.pdf4517484241515548Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Dentistry0,6490,649info:eu-repo/semantics/openAccess2024-09-27T14:05:34Zoai:repositorio.unesp.br:11449/73492Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:05:34Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
title In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
spellingShingle In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
Basso, Fernanda G.
title_short In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
title_full In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
title_fullStr In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
title_full_unstemmed In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
title_sort In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
author Basso, Fernanda G.
author_facet Basso, Fernanda G.
Pansani, Taisa N. [UNESP]
Turrioni, Ana Paula S. [UNESP]
Bagnato, Vanderlei S.
Hebling, Josimeri [UNESP]
De Souza Costa, Carlos A. [UNESP]
author_role author
author2 Pansani, Taisa N. [UNESP]
Turrioni, Ana Paula S. [UNESP]
Bagnato, Vanderlei S.
Hebling, Josimeri [UNESP]
De Souza Costa, Carlos A. [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Basso, Fernanda G.
Pansani, Taisa N. [UNESP]
Turrioni, Ana Paula S. [UNESP]
Bagnato, Vanderlei S.
Hebling, Josimeri [UNESP]
De Souza Costa, Carlos A. [UNESP]
description The aim of this study was to determine adequate energy doses using specific parameters of LLLT to produce biostimulatory effects on human gingival fibroblast culture. Cells (3 10 4 cells/cm 2) were seeded on 24-well acrylic plates using plain DMEM supplemented with 10 fetal bovine serum. After 48-hour incubation with 5 CO2 at 37C, cells were irradiated with a InGaAsP diode laser prototype (LASERTable; 780 3 nm; 40mW) with energy doses of 0.5, 1.5, 3, 5, and 7J/cm 2. Cells were irradiated every 24h totalizing 3 applications. Twenty-four hours after the last irradiation, cell metabolism was evaluated by the MTT assay and the two most effective doses (0.5 and 3J/cm 2) were selected to evaluate the cell number (trypan blue assay) and the cell migration capacity (wound healing assay; transwell migration assay). Data were analyzed by the Kruskal-Wallis and Mann-Whitney nonparametric tests with statistical significance of 5. Irradiation of the fibroblasts with 0.5 and 3J/cm 2 resulted in significant increase in cell metabolism compared with the nonrradiated group (P 0.05). Both energy doses promoted significant increase in the cell number as well as in cell migration (P 0.05). These results demonstrate that, under the tested conditions, LLLT promoted biostimulation of fibroblasts in vitro. Copyright © 2012 Fernanda G. Basso et al.
publishDate 2012
dc.date.none.fl_str_mv 2012-08-17
2014-05-27T11:26:56Z
2014-05-27T11:26:56Z
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/10.1155/2012/719452
International Journal of Dentistry.
1687-8728
1687-8736
http://hdl.handle.net/11449/73492
10.1155/2012/719452
2-s2.0-84864959975
2-s2.0-84864959975.pdf
4517484241515548
url http://dx.doi.org/10.1155/2012/719452
http://hdl.handle.net/11449/73492
identifier_str_mv International Journal of Dentistry.
1687-8728
1687-8736
10.1155/2012/719452
2-s2.0-84864959975
2-s2.0-84864959975.pdf
4517484241515548
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Dentistry
0,649
0,649
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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 repositoriounesp@unesp.br
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