Effect of a novel bioceramic root canal sealer on the angiogenesis-enhancing potential of assorted human odontogenic stem cells compared with principal tricalcium silicate-based cements

Abstract Objective: This study evaluated the angiogenesis-enhancing potential of a tricalcium silicate-based mineral trioxide aggregate (ProRoot MTA), Biodentine, and a novel bioceramic root canal sealer (Well-Root ST) in human dental pulp stem cells (hDPSCs), human periodontal ligament stem cells (hPLSCs), and human tooth germ stem cells (hTGSCs). Methodology: Dulbecco's modified Eagle's medium was conditioned for 24 h by exposure to ProRoot MTA, Biodentine, or Well-Root ST specimens (prepared according to the manufacturers' instructions). The cells were cultured in these conditioned media and their viability was assessed with 3-(4,5-dimethyl-thiazol-2-yl)-5-(3-carboxy-methoxy-phenyl)-2-(4-sulfo-phenyl)-2H tetrazolium (MTS) on days 1, 3, 7, 10, and 14. Angiogenic growth factors [platelet-derived growth factor (PDGF), basic fibroblast growth factor (FGF-2), and vascular endothelial growth factor (VEGF)] were assayed by sandwich enzyme-linked immunosorbent assay (ELISA) on days 1, 7, and 14. Human umbilical vein endothelial cell (HUVEC) migration assays were used to evaluate the vascular effects of the tested materials at 6-8 h. Statistical analyses included Kruskal-Wallis, Mann-Whitney U, and Friedman and Wilcoxon signed rank tests. Results: None of tricalcium silicate-based materials were cytotoxic and all induced a similar release of angiogenic growth factors (PDGF, FGF-2, and VEGF) (p>0.05). The best cell viability was observed for hDPSCs (p<0.05) with all tricalcium silicate-based materials at day 14. Tube formation by HUVECs showed a significant increase with all tested materials (p<0.05). Conclusion: The tricalcium silicate-based materials showed potential for angiogenic stimulation of all stem cell types and significantly enhanced tube formation by HUVECs.

Comparative evaluation of postoperative pain intensity after single-visit and multiple-visit retreatment cases: a prospective randomized clinical trial / Avaliação comparativa da intensidade da dor pos-operatoria após casos de retratamento em sessao unica ou multipla: estudo clínico randomizado prospectivo

Objectives: This study was designed to evaluate postoperative pain after endodontic retreatment. Material and Methods: Asymptomatic, multirooted molar & premolar teeth requiring retreatment with 2­5 mm periapical lesions were included. Seventy-eight teeth were randomly placed in four groups (n=20): single-visit (control, group 1), Ledermix (group 2), metronidazole, ciprofloxacin, minocycline mixture (group 3), calcium hydroxide (group 4). The postoperative pain was recorded using a VAS at 6, 12, 24, and 48 h after retreatment. Statistical evaluation was performed using TwoWay Repeated Measures ANOVA and Tukey test. Results: Mild pain occurred in 67.5%, moderate in 30%, and flare-ups in 2.5%, and there was a significant difference between the groups (p <0.01). Significantly lower postoperative pain was observed in TAP and CaOH2 groups (p <0.05). In the 6, 12, and 24 h intervals, there was a significant difference in the pain levels (p <0.05). Conclusion: TAP and CaOH2 are effective for reducing postoperative pain after retreatment. (AU)

Objetivo: Este estudo foi projetado para avaliar a dor pós-operatória após o retratamento endodôntico. Material e Métodos: Foram incluídos dentes molares e pré-molares multirradiculados e assintomáticos que necessitavam de retratamento com lesões periapicais de 2-5 mm. Setenta e oito dentes foram distribuídos aleatoriamente em quatro grupos (n = 20): sessão única (controle, grupo I), Ledermix (grupo II), metronidazol, ciprofloxacina, mistura de minociclina (grupo III), hidróxido de cálcio (grupo IV). A dor pós-operatória foi registrada usando um VAS às 6, 12, 24 e 48 h após o retratamento. A análise estatística foi realizada utilizando ANOVA de dois fatores para medidas repetidas e teste de Tukey. Resultados: Ocorreu dor leve em 67,5%, moderada em 30% e agudizações 2,5%, e houve diferença significativa entre os grupos (p <0,01). Foi observada dor pós-operatória significativamente menor nos grupos TAP e hidróxido de cálcio (p <0,05). Nos intervalos de 6, 12 e 24 h, houve diferença significativa nos níveis de dor (p <0,05). Conclusão: TAP e hidróxido de cálcio são eficazes para reduzir a dor pós-operatória após o retratamento.(AU)

Effects of intracanal medicaments and the remaining cavity wall on fracture strength of endodontically treated molars / Efeitos dos medicamentos intracanais e do muro de cavidade remanescente na força de fratura dos molares endodonticamente tratados

Objective: The aim of this study was to investigate the effects of the short-term intracanal application of two medicaments on the fracture strength of root-filled molar teeth with different levels of tooth structure loss. Material and Methods: Standard access cavities of totally 84 intact maxillary molar teeth were prepared in 72 teeth and were divided into 3 main groups. Standard access cavities were kept in the first group, while mesio-occlusal-distal cavities (MOD) were prepared in the second and third groups. One-half of the palatinal walls were removed in the third group. Twelve sound teeth were used in the fourth group as control. Each group was then assigned into two subgroups according to the medicament used (n=12): 2% chlorhexidine gel and calcium hydroxide. Samples were stored at 37°C and 100% humidity for 1 week. Then the teeth were inserted into a universal testing machine and vertically loaded (5 mm/min) from the occlusal surface. The data was recorded in Newtons and statistically evaluated using a Univariate ANOVA and a Tukey as post hoc test. Results: A significant difference was found among the test groups (p <0.01). No significant difference was found according to the medicament used (p>0.05), however the number of remaining walls significantly affected the fracture strength (p <0.01). The first group with access cavity showed mostly repairable fractures (60%­80%) whereas the others showed mostly nonrepairable fracture patterns s (60%­90%). Conclusion: In conclusion, the fracture strength of endodontically treated teeth is related to the structure loss rather than the intracanal medicament used. (AU)

Objetivo: O objetivo deste estudo foi investigar os efeitos da aplicação intracanal de curto prazo de dois medicamentos sobre a resistência à fratura de dentes molares preenchidos com raízes com diferentes níveis de perda de estrutura dentária. Material e Métodos: cavidades de acesso padrão de totalmente 84 dentes molar maxilares intactos foram preparadas em 72, dentes e foram divididas em 3 grupos principais. As cavidades de acesso padrão foram mantidas no primeiro grupo, enquanto as cavidades mesooclusais-distal (MOD) foram preparadas no segundo e terceiro grupos. A metade das paredes palatinas foi removida no terceiro grupo. Doze dentes de som foram utilizados no quarto grupo como controle. Cada grupo foi então atribuído em dois subgrupos de acordo com o medicamento utilizado (n = 12): 2% de gel de clorhexidina e hidróxido de cálcio. As amostras foram armazenadas a 37 ° C e 100% de umidade por 1 semana. Em seguida, os dentes foram inseridos em uma máquina de teste universal e carregados verticalmente (5 mm / min) da superfície oclusal. Os dados foram registrados em Newtons e avaliados estatisticamente usando uma ANOVA Univariada e um Tukey como teste post hoc. Resultados: uma diferença significativa foi encontrada entre os grupos de teste (p <0,01), no entanto, o número de paredes restantes afetou significativamente a resistência à fratura (p <0,01). O primeiro grupo com cavidade de acesso apresentou fracturas principalmente reparáveis (60% -80%), enquanto as demais apresentaram padrões de fratura não reparáveis (60% -90%). Conclusão: Em conclusão, a resistência à fratura dos dentes tratados endodonticamente está relacionada à perda da estrutura em vez do medicamento intracanal utilizado.(AU)