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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Effect of hydrogen-peroxide-mediated oxidative stress on human dental pulp cells

Texto completo
Autor(es):
Soares, Diana Gabriela [1] ; Basso, Fernanda Goncalves [2] ; Hebling, Josimeri [3] ; de Souza Costa, Carlos Alberto [2]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] Univ Estadual Paulista, Araraquara Sch Dent, Dept Dent Mat & Prosthodont, BR-14801903 Araraquara, SP - Brazil
[2] Univ Estadual Paulista, Araraquara Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP - Brazil
[3] Univ Estadual Paulista, Araraquara Sch Dent, Dept Orthodont & Pediat Dent, BR-14801903 Araraquara, SP - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: Journal of Dentistry; v. 43, n. 6, p. 750-756, JUN 2015.
Citações Web of Science: 8
Resumo

Objectives: To evaluate the effect of the oxidative stress on human dental pulp cells (HDPCs) promoted by toxic concentrations of hydrogen peroxide (H2O2) on its odontoblastic differentiation capability through time. Methods: HDPCs were exposed to two different concentrations of H2O2 (0.1 and 0.3 mg/ml) for 30 min. Thereafter, cell viability (MTT assay) and oxidative stress generation (H(2)DCFDA fluorescence assay) were immediately evaluated. Data were compared with those for alkaline phosphatase (ALP) activity (thymolphthalein assay) and mineralized nodule deposition (alizarin red) by HDPCs cultured for 7 days in osteogenic medium. Results: A significant reduction in cell viability and oxidative stress generation occurred in the H2O2-treated cells when compared with negative controls (no treatment), in a concentration-dependent fashion. Seven days after H2O2 treatment, the cells showed significant reduction in ALP activity compared with negative control and no mineralized nodule deposition. Conclusion: Both concentrations of H2O2 were toxic to the cells, causing intense cellular oxidative stress, which interfered with the odontogenic differentiation capability of the HDPCs. Clinical significance: The intense oxidative stress on HDPCs mediated by H2O2 at toxic concentrations promotes intense reduction on odontoblastic differentiation capability in a 7-day evaluation period, which may alter the initial pulp healing capability in the in vivo situation. (C) 2014 Elsevier Ltd. All rights reserved. (AU)

Processo FAPESP: 13/23520-0 - Bioatividade de scaffolds experimentais a base de quitosana e colágeno sobre cultura de células pulpares humanas
Beneficiário:Diana Gabriela Soares dos Passos
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado