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Root canal dressings for revascularization influence in vitro mineralization of apical papilla cells
Rahhal, Juliana Garuba; Rovai, Emanuel da Silva; Holzhausen, Marinella; Caldeira, Celso Luiz; Santos, Carlos Ferreira dos; Sipert, Carla Renata.
  • Rahhal, Juliana Garuba; Universidade de São Paulo. Faculdade de Odontologia. Departamento de Dentística. São Paulo. BR
  • Rovai, Emanuel da Silva; Universidade de São Paulo. Faculdade de Odontologia. Departamento de Estomatologia. São Paulo. BR
  • Holzhausen, Marinella; Universidade de São Paulo. Faculdade de Odontologia. Departamento de Estomatologia. São Paulo. BR
  • Caldeira, Celso Luiz; Universidade de São Paulo. Faculdade de Odontologia. Departamento de Dentística. São Paulo. BR
  • Santos, Carlos Ferreira dos; Universidade de São Paulo. Faculdade de Odontologia de Bauru. Departamento de Ciências Biológicas. Bauru. BR
  • Sipert, Carla Renata; Universidade de São Paulo. Faculdade de Odontologia. Departamento de Dentística. São Paulo. BR
J. appl. oral sci ; 27: e20180396, 2019. graf
Article in English | LILACS, BBO | ID: biblio-1002404
ABSTRACT
Abstract Endodontic revascularization is based on cell recruitment into the necrotic root canal of immature teeth after chemical disinfection. The clinical outcome depends on the ability of surviving cells from the apical tissue to differentiate and promote hard tissue deposition inside the dentinal walls. Objective To investigate the effect of calcium hydroxide (CH) and modified triple antibiotic paste (mTAP - ciprofloxacin, metronidazole and cefaclor) on the viability and mineralization potential of apical papilla cells (APC) in vitro . Material and Methods APC cultures were kept in contact with CH or mTAP (250-1000 µg/mL) for 5 days, after which cell viability was assessed using 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Next, APCs were subjected to CH or mTAP at 250 µg/mL for 5 days before inducing the differentiation assay. After 14 and 21 days, calcium deposition was assessed by the Alizarin Red S staining method, followed by elution and quantification using spectrophotometry. Data were analyzed using ANOVA followed by Tukey post hoc test. Results CH induced cell proliferation, whereas mTAP showed significant cytotoxicity at all concentrations tested. APC treated with CH demonstrated improved mineralization capacity at 14 days, while, for mTAP, significant reduction on the mineralization rate was observed for both experimental periods (14 and 21 days). Conclusion Our findings showed that CH induces cell proliferation and improves early mineralization, whereas mTAP was found cytotoxic and reduced the mineralization potential in vitro of APCs.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Root Canal Irrigants / Calcium Hydroxide / Dental Papilla / Anti-Bacterial Agents Type of study: Evaluation studies Limits: Humans Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2019 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Root Canal Irrigants / Calcium Hydroxide / Dental Papilla / Anti-Bacterial Agents Type of study: Evaluation studies Limits: Humans Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2019 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR