Viability and oxidative stress of dental pulp cells after indirect application of chemomechanical agents: An in vitro study

Author:

Lins‐Candeiro Caio Luiz1,Paranhos Luiz Renato2,de Oliveira Neto Nilson Ferreira1,Ribeiro Rafael Antônio Oliveira3,de‐Souza‐Costa Carlos Alberto4ORCID,Guedes Fernanda Rodrigues1,da Silva Washington Henrique Themoteo1,Turrioni Ana Paula5ORCID,Santos Filho Paulo César de Freitas6

Affiliation:

1. Post‐graduation Program in Dentistry, School of Dentistry Federal University of Uberlândia Uberlândia Minas Gerais Brazil

2. Division of Preventive and Community Dentistry, School of Dentistry Federal University of Uberlândia Minas Gerais Brazil

3. Department of Dental Materials and Prosthesis, School of Dentistry São Paulo State University Júlio de Mesquita Filho Araraquara São Paulo Brazil

4. Department of Physiology and Pathology, School of Dentistry São Paulo State University Júlio de Mesquita Filho Araraquara São Paulo Brazil

5. Division of Pediatric Dentistry and Orthodontics, School of Dentistry Federal University of Uberlândia Uberlândia Minas Gerais Brazil

6. Division of Restorative Dentistry and Dental Materials, School of Dentistry Federal University of Uberlândia Uberlândia Minas Gerais Brazil

Abstract

AbstractAimThis study evaluated the transdentinal cytotoxic effects of enzymatic agents (EA) for chemomechanical carious tissue removal on human dental pulp cells.MethodologyThe groups were based on the performed dentine treatments (n = 8): G1: Positive Control (PC ‐ no treatment); G2: Negative Control (NC ‐ 35% H2O2 for 2 min); G3: Brix 3000™ (BX) for 30 s; G4: BX for 2 min; G5: Papacarie Duo™ (PD) for 30 s; G6: PD for 2 min. The cells were evaluated for viability (VB; MTT assay) and production of reactive oxygen species (ROS; DCFH‐DA assay) and nitric oxide (NO; Griess reagent). A scanning electron microscope provided morphological chemical analyses and energy‐dispersive X‐ray spectroscopy. The data were submitted to the one‐way anova statistical test complemented by Tukey (p < .05).ResultsCell viability decreased by 21.1% and 58.4% in G5 and G6, respectively. ROS production in G3 and G4 maintained basal levels but increased by 171.2% and 75.1% in G5 and G6, respectively.ConclusionsThe Brix3000™ enzymatic agent did not cause indirect cytotoxic effects on pulp cells, regardless of the application time. Conversely, Papacarie Duo™ reduced viability and increased ROS production by pulp cells.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado de Minas Gerais

Publisher

Wiley

Subject

General Dentistry

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