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Concentrated MTA Repair HP reduced biofilm and can cause reparative action at a distance.
Silva, Poliana Amanda Oliveira; Lima, Stella Maris de Freitas; Martins, Danilo César Mota; Amorim, Ingrid Aquino; Lacorte, Cristiano; de Almeida, Jeesser Alves; Franco, Octávio Luiz; Rezende, Taia Maria Berto.
Afiliação
  • Silva PAO; Programa de Pós-graduação em Ciências da Saúde, Universidade de Brasília, Brasília, Brazil.
  • Lima SMF; Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, Brasília, Brazil.
  • Martins DCM; Curso de Odontologia, Universidade Católica de Brasília, Brasília, Brazil.
  • Amorim IA; Programa de Pós-graduação em Ciências da Saúde, Universidade de Brasília, Brasília, Brazil.
  • Lacorte C; Curso de Odontologia, Centro Universitário ICESP, Brasília, Brazil.
  • de Almeida JA; Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, Brasília, Brazil.
  • Franco OL; Curso de Odontologia, Centro Universitário UNIEURO, Brasília, Brazil.
  • Rezende TMB; Laboratório de Biologia Sintética, Embrapa Recursos Genéticos e Biotecnologia, Brasília, Brazil.
Int Endod J ; 54(10): 1925-1936, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34164821
AIM: To evaluate in vitro whether MTA Repair HP can induce repair processes at a distance, including its effects on biofilm, cell viability, migration, production of TGF-ß, phosphate and ALP, evaluated through MTA diluted extracts. METHODOLOGY: Initially, antibacterial tests were performed with the bacterium Streptococcus mutans (ATCC 25175) in the presence of MTA extracts (dilutions of 1:1, 1:2 and 1:4). Growth inhibition assay by microdilution in broth, antibiofilm plate assay of young biofilm and antibiofilm assay in confocal microscopy of mature biofilm were carried out. Then, pulp cells were stimulated in the presence of several MTA dilutions, and cell viability (MTT assay), proliferation and migration capacity (scratch assay) were evaluated. To evaluate the capacity of 1:1, 1:2 and 1:4 dilutions of MTA Repair HP to promote the production of important agents of odontogenic differentiation and mineralization, ALP activity, TGF-ß secretion and phosphate quantification were measured. Statistical differences were verified using one-way and two-way anova and Tukey's post-tests. RESULTS: The test dilutions of MTA Repair HP did not inhibit planktonic S. mutans growth but were able to reduce young and mature S. mutans biofilm (p < 0.001). In addition, none of the MTA Repair HP dilutions was cytotoxic for pulp cells. The 1:2 and 1:4 dilutions of MTA Repair HP induced migration and proliferation of pulp cells (p < 0.05). ALP activity and TGF-ß secretion were independent of the tested dilution (p < 0.001). Diluted 1:4 MTA Repair HP produced less phosphate than the more concentrated 1:1 and 1:2 MTA dilutions (p < 0.001). CONCLUSIONS: Undiluted MTA Repair HP reduced S. mutans biofilm, when compared to 1:2 and 1:4 MTA dilutions. Furthermore, none of the tested dilutions was cytotoxic to pulp cells. MTA Repair HP promoted cell migration and proliferation at a distance, assessed through the dilution of the MTA. Even from a distance, MTA Repair HP has the ability to participate in some events related to repair, such as migration, proliferation and TGF production.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Materiais Restauradores do Canal Radicular / Compostos de Cálcio Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Materiais Restauradores do Canal Radicular / Compostos de Cálcio Idioma: En Ano de publicação: 2021 Tipo de documento: Article