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Cytotoxicity of dimethyl sulfoxide (DMSO) in direct contact with odontoblast-like cells.
Hebling, J; Bianchi, L; Basso, F G; Scheffel, D L; Soares, D G; Carrilho, M R O; Pashley, D H; Tjäderhane, L; de Souza Costa, C A.
Afiliación
  • Hebling J; UNESP - Univ Estadual Paulista, Araraquara School of Dentistry, Department of Pediatric Dentistry and Orthodontics, Araraquara, SP, Brazil. Electronic address: jhebling@foar.unesp.br.
  • Bianchi L; UNESP - Univ Estadual Paulista, Araraquara School of Dentistry, Department of Pediatric Dentistry and Orthodontics, Araraquara, SP, Brazil.
  • Basso FG; UNESP - Univ Estadual Paulista, Araraquara School of Dentistry, Department of Pediatric Dentistry and Orthodontics, Araraquara, SP, Brazil.
  • Scheffel DL; UNESP - Univ Estadual Paulista, Araraquara School of Dentistry, Department of Pediatric Dentistry and Orthodontics, Araraquara, SP, Brazil.
  • Soares DG; UNESP - Univ Estadual Paulista, Araraquara School of Dentistry, Department of Pediatric Dentistry and Orthodontics, Araraquara, SP, Brazil.
  • Carrilho MR; Anhanguera University of São Paulo (UNIAN), São Paulo, Brazil.
  • Pashley DH; Georgia Regents University, College of Dental Medicine, Department of Oral Biology, Augusta, GA, USA.
  • Tjäderhane L; Institute of Dentistry, University of Oulu, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • de Souza Costa CA; UNESP - Univ Estadual Paulista, Araraquara School of Dentistry, Departament of Physiology and Pathology, Araraquara, SP, Brazil.
Dent Mater ; 31(4): 399-405, 2015 Apr.
Article en En | MEDLINE | ID: mdl-25681221
ABSTRACT

OBJECTIVES:

To evaluate the cytotoxicity of dimethyl sulfoxide (DMSO) on the repair-related activity of cultured odontoblast-like MDPC-23 cells.

METHODS:

Solutions with different concentrations of DMSO (0.05, 0.1, 0.3, 0.5 and 1.0 mM), diluted in culture medium (DMEM), were placed in contact with MDPC-23 cells (5 × 104 cells/cm(2)) for 24 h. Eight replicates (n = 8) were prepared for each solutions for the following methods of

analysis:

violet crystal dye for cell adhesion (CA), quantification of total protein (TP), alizarin red for mineralization nodules formation (MN) and cell death by necrosis (flow cytometry); while twelve replicates (n = 12) were prepared for viable cell number (Trypan Blue) and cell viability (MTT assay). Data were analyzed by ANOVA and Tukey or Kruskal-Wallis and Mann-Whitney's tests (p < 0.05).

RESULTS:

Cell viability, adhesion and percentage of cell death by necrosis were not affected by DMSO at any concentration, with no statistical significant difference among the groups. A significant reduction in total protein production was observed for 0.5 and 1.0 mM of DMSO compared to the control while increased mineralized nodules formation was seen only for 1.0 mM DMSO.

SIGNIFICANCE:

DMSO caused no or minor cytotoxic effects on the pulp tissue repair-related activity of odontoblast-like cells.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dimetilsulfóxido / Depuradores de Radicales Libres / Odontoblastos Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dimetilsulfóxido / Depuradores de Radicales Libres / Odontoblastos Idioma: En Año: 2015 Tipo del documento: Article