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Protective Effect of Alpha-Tocopherol Isomer from Vitamin E against the H(2)O(2) Induced Toxicity on Dental Pulp Cells

The aim of this study was to evaluate the protective effects of different concentrations of vitamin E alpha-tocopherol (α-T) isomer against the toxicity of hydrogen peroxide (H(2)O(2)) on dental pulp cells. The cells (MDPC-23) were seeded in 96-well plates for 72 hours, followed by treatment with 1,...

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Detalles Bibliográficos
Autores principales: Vargas, Fernanda da Silveira, Soares, Diana Gabriela, Ribeiro, Ana Paula Dias, Hebling, Josimeri, De Souza Costa, Carlos Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918697/
https://www.ncbi.nlm.nih.gov/pubmed/24587995
http://dx.doi.org/10.1155/2014/895049
Descripción
Sumario:The aim of this study was to evaluate the protective effects of different concentrations of vitamin E alpha-tocopherol (α-T) isomer against the toxicity of hydrogen peroxide (H(2)O(2)) on dental pulp cells. The cells (MDPC-23) were seeded in 96-well plates for 72 hours, followed by treatment with 1, 3, 5, or 10 mM α-T for 60 minutes. They were then exposed or not to H(2)O(2) for 30 minutes. In positive and negative control groups, the cells were exposed to culture medium with or without H(2)O(2) (0.018%), respectively. Cell viability was evaluated by MTT assay (Kruskal-Wallis and Mann-Whitney tests; α = 5%). Significant reduction of cell viability (58.5%) was observed in positive control compared with the negative control. Cells pretreated with α-T at 1, 3, 5, and 10 mM concentrations and exposed to H(2)O(2) had their viability decreased by 43%, 32%, 25%, and 27.5%, respectively. These values were significantly lower than those observed in the positive control, thereby showing a protective effect of α-T against the H(2)O(2) toxicity. Overall, the vitamin E α-T isomer protected the immortalized MDPC-23 pulp cells against the toxic effects of H(2)O(2). The most effective cell protection was provided by 5 and 10 mM concentrations of α-T.