In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , |
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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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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1813546484386234368 |