Literature DB >> 28801810

Effects of PBM in different energy densities and irradiance on maintaining cell viability and proliferation of pulp fibroblasts from human primary teeth.

Nádia Carolina Teixeira Marques1, Natalino Lourenço Neto1, Mariel Tavares Oliveira Prado1, Luciana Lourenço Ribeiro Vitor1, Rodrigo Cardoso Oliveira2, Vivien Thiemy Sakai3, Carlos Ferreira Santos2, Maria Aparecida Andrade Moreira Machado1, Thais Marchini Oliveira4.   

Abstract

This study aimed to compare the effects of photobiomodulation (PBM) in different energy densities and irradiances on maintaining cell viability, and proliferation of pulp fibroblasts from human primary teeth (HPF) were cultured in DMEM and used between the fourth and eighth passages. Then, HPF were irradiated with the following different energy densities: 1.25 J/cm2 (a), 2.50 J/cm2 (b), 3.75 J/cm2 (c), 5.00 J/cm2 (d), and 6.25 J/cm2 (e); but varying either the time of irradiation (groups 1a-1e) or the output power (groups 2a-2e). Positive (groups 1f and 2f) and negative controls (groups 1g and 2g), respectively, comprised non-irradiated cells grown in regular nutritional conditions (10% fetal bovine serum [FBS]) and under nutritional deficit (1% FBS). Cell viability and proliferation were respectively assessed through MTT and crystal violet (CV) assays at 24, 48, and 72 h after irradiation. Statistical analysis was performed by two-way ANOVA, followed by Tukey test (P < 0.05). The negative controls showed significantly lower viability in relation to most of the corresponding subgroups, both for MTT and CV assays. For both assays, the intragroup comparison showed that the periods of 24 h exhibited lower viability than the periods of 48 and 72 h for most of the subgroups, except the negative controls with lower viability. The different irradiation protocols (equal energy densities applied with different irradiances) showed no statistically significant differences on cell viability and proliferation at the evaluated periods. The proposed PBM in different energy densities and irradiance did not affect the viability and proliferation of pulp fibroblasts from human primary teeth.

Entities:  

Keywords:  Cell proliferation; Cell survival; Culture techniques; Dental pulp; Low-level light therapy; Tooth, deciduous

Mesh:

Year:  2017        PMID: 28801810     DOI: 10.1007/s10103-017-2301-z

Source DB:  PubMed          Journal:  Lasers Med Sci        ISSN: 0268-8921            Impact factor:   3.161


  32 in total

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4.  Quantification of cells cultured on 96-well plates.

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5.  Clinical, radiographic and histologic analysis of the effects of pulp capping materials used in pulpotomies of human primary teeth.

Authors:  T M Oliveira; A B S Moretti; V T Sakai; N Lourenço Neto; C F Santos; M A A M Machado; R C C Abdo
Journal:  Eur Arch Paediatr Dent       Date:  2013-04-03

6.  Comparison of the low level laser therapy effects on cultured human gingival fibroblasts proliferation using different irradiance and same fluence.

Authors:  L Almeida-Lopes; J Rigau; R A Zângaro; J Guidugli-Neto; M M Jaeger
Journal:  Lasers Surg Med       Date:  2001       Impact factor: 4.025

7.  Effect of low-level Er:YAG laser irradiation on cultured human gingival fibroblasts.

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8.  Effect of low-power laser irradiation on protein synthesis and ultrastructure of human gingival fibroblasts.

Authors:  Márcia M Marques; Aymann N Pereira; Neusa A Fujihara; Fernando N Nogueira; Carlos P Eduardo
Journal:  Lasers Surg Med       Date:  2004       Impact factor: 4.025

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

Authors:  Fernanda G Basso; Taisa N Pansani; Ana Paula S Turrioni; Vanderlei S Bagnato; Josimeri Hebling; Carlos A de Souza Costa
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10.  CCL3 and CXCL12 production in vitro by dental pulp fibroblasts from permanent and deciduous teeth stimulated by Porphyromonas gingivalis LPS.

Authors:  Carla Renata Sipert; Ana Carolina de Faria Morandini; Karin Cristina da Silva Modena; Thiago José Dionísio; Maria Aparecida Andrade Moreira Machado; Sandra Helena Penha de Oliveira; Ana Paula Campanelli; Carlos Ferreira Santos
Journal:  J Appl Oral Sci       Date:  2013 Mar-Apr       Impact factor: 2.698

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1.  Does the application of GaAlAs laser and platelet-rich plasma induce cell proliferation and increase alkaline phosphatase activity in human dental pulp stem cells?

Authors:  Maryam Bidar; Aminmohammad Bahlakeh; Mahmoud Mahmoudi; Farzaneh Ahrari; Reza Shahmohammadi; Hamid Jafarzadeh
Journal:  Lasers Med Sci       Date:  2021-01-18       Impact factor: 3.161

2.  Effect of single and multiple doses of low-level laser therapy on viability and proliferation of stem cells from human exfoliated deciduous teeth (SHED).

Authors:  Luciano Aparecido Almeida-Junior; Nádia Carolina Teixeira Marques; Mariel Tavares de Oliveira Prado; Thais Marchini Oliveira; Vivien Thiemy Sakai
Journal:  Lasers Med Sci       Date:  2019-07-02       Impact factor: 3.161

3.  Could the photobiomodulation therapy induce angiogenic growth factors expression from dental pulp cells?

Authors:  Mariel Tavares Bergamo; Luciana Lourenço Ribeiro Vitor; Thiago José Dionísio; Nádia Carolina Teixeira Marques; Rodrigo Cardoso Oliveira; Eloá Cristina Passucci Ambrosio; Vivien Thiemy Sakai; Carlos Ferreira Santos; Natalino Lourenço Neto; Maria Aparecida Andrade Moreira Machado; Thais Marchini Oliveira
Journal:  Lasers Med Sci       Date:  2021-04-01       Impact factor: 3.161

4.  Laser treatment contributes to maintain membrane integrity in stem cells from human exfoliated deciduous teeth (shed) under nutritional deficit.

Authors:  Paula Corrêa Silveira da Silva; Nelson Pereira Marques; Marcella Tassi Farina; Thais Marchini Oliveira; Cristiane Duque; Nádia Carolina Teixeira Marques; Vivien Thiemy Sakai
Journal:  Lasers Med Sci       Date:  2018-07-06       Impact factor: 3.161

  4 in total

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