RESUMO
Multiple side effects related to bleaching were found to occur in the dental pulp tissue, including decreased cell metabolism and viability. In this work we evaluated the in vitro diffusion capacity, cytotoxicity and biocompatibility of four commercial bleaching products on stem cells from human dental pulp (hDPSCs). Two commercial bleaching gels hydrogen peroxide-based (HP), Norblanc Office 37.5% (Nor-HP) and Opalescence Boost 40% (Opal-HP) were applied for 30 min to enamel/dentine discs. Another two gels from the same manufacturers, 16% carbamide peroxide-based (CP), Norblanc Home (Nor-CP) and Opalescence CP 16% (Opal-CP), were applied for 90 min. The diffusion of HP was analysed by fluorometry. Cytotoxicity was determined using the MTT assays, the determination of apoptosis, immunofluorescence assays and intracellular reactive oxygen species (ROS) level. Tissue inflammatory reactions were evaluated histopathologically in rats. Statistical differences were performed by one-way ANOVA and Bonferroni post-test (α < 0.05). Normon products showed lower cytotoxicity and diffusion capacity than the Ultradent products. A high intracellular ROS level was measured in hDPSCs after exposure to Opal-HP. Finally, a severe necrosis of both coronal and radicular pulp was observed with Opal-HP. Similar concentrations of hydrogen peroxide and carbamide peroxide in a variety of bleaching products exhibited different responses in cells and dental pulp tissue, suggesting that bleaching products contain unknown agents that could influence their toxicity.
Assuntos
Polpa Dentária/efeitos dos fármacos , Células-Tronco/efeitos dos fármacos , Clareadores Dentários/toxicidade , Adulto , Animais , Anti-Infecciosos , Peróxido de Carbamida/toxicidade , Difusão , Feminino , Humanos , Peróxido de Hidrogênio/toxicidade , Inflamação , Masculino , Microscopia Eletrônica de Varredura , Peróxidos/toxicidade , Ratos , Ratos Wistar , Clareamento Dental/métodos , Adulto JovemRESUMO
Previous studies have demonstrated the side effects of tooth whiteners on the gastric mucosa. However, the impact of dental bleaching products on the liver, kidney, and heart remains obscure. The present study investigated the toxic potential of 35% carbamide peroxide (CPO) containing tooth whitening product (TWP) on the liver, kidney, heart, and stomach of mice, pointing to the role of oxidative stress and inflammation. Mice received 250 or 500 mg/kg body weight CPO-TWP orally for 3 weeks and samples were collected for analyses. Both doses of CPO-TWP induced a significant increase in circulating liver, kidney, and heart function markers. CPO-TWP-administered mice showed several histological alterations and a significant increase in liver, kidney, heart, and stomach lipid peroxidation levels along with diminished glutathione, superoxide dismutase, and catalase. In addition, administration of CPO-TWP provoked anemia, leukocytosis, and a significant increase in circulating levels of pro-inflammatory cytokines. In conclusion, exposure to 35% CPO-TWP induced functional, histological, and hematological alterations, oxidative stress, and inflammation in mice. Therefore, the frequent use of tooth bleaching agents should be monitored very carefully to avoid the application of excess amounts as well as the intake.