Detalhes do Documento

Rat tissue reaction and cytokine production induced by antimicrobial photodynamic therapy

Autor(es): Sivieri-Araujo, Gustavo [UNESP] ; Queiroz, Índia Olinta de Azevedo [UNESP] ; Dal Fabbro, Renan [UNESP] ; Esteves, Fernanda [UNESP] ; Cintra, Luciano Tavares Angelo [UNESP] ; Duarte, Paulo Carvalho Tobias [UNESP] ; Bagnato, Vanderlei Salvador ; Oliveira, Sandra Helena Penha [UNESP] ; Gomes Filho, João Eduardo [UNESP]

Data: 2018

Identificador Persistente: http://hdl.handle.net/11449/178837

Origem: Oasisbr

Assunto(s): Antimicrobial photodynamic therapy; Biocompatibility; Cytokine; Endodontic treatment; Root canal irrigants; Antimicrobial photodynamic therapy; Antimicrobial photodynamic therapy; Biocompatibility; Biocompatibility; Cytokine; Cytokine; Endodontic treatment; Endodontic treatment; Root canal irrigants; Root canal irrigants


Descrição

Made available in DSpace on 2018-12-11T17:32:18Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-06-01

Background The antimicrobial photodynamic therapy (aPDT) inactivates the target cell via reactions among the photosensitizer (PS), Laser or Led and O2. The aim of this study was to evaluate the tissue reaction and cytokine production promoted by aPDT with curcumin photosensitizer. Methods Polyethylene tubes containing saline solution (control), 5% sodium hypochlorite (NaOCl) and aPDT with curcumin PS 500 mg/L, were implanted into dorsal connective tissue of Wistar rats. After 7, 15, 30, 60 and 90 days of implantation, the animals were euthanized and the tubes with surrounding tissues were removed. The specimens were divided in two part, one half was processed, fixed and prepared for histological analysis by staining with hematoxylin and eosin. The other half was collected for IL-1β and IL-6 cytokine production using ELISA assay. The results were statistically analyzed by Kruskal-Wallis test followed by Dunn test (p < 0.05) for tissue reaction and ANOVA followed by Bonferroni's correction (p < 0.05) for ELISA. Results All groups showed severe tissue reactions at 7 days, whilst a significantly decrease by time was observed. Regarding to cytokine production, aPDT increases the IL-1β levels in all periods of time (p < 0.05). However, for IL-6 levels, the highest value was observed with aPDT on the 90th day (p < 0.05). Conclusions aPDT with curcumin PS 500 mg/L demonstrated biocompatibility similar to saline solution and induced the IL-1β and IL-6 cytokines production.

Department of Restorative Dentistry Discipline of EndodonticsDiscipline of Endodontics São Paulo State University (Unesp) School of Dentistry

Optics Group Physics Institute of São Carlos University of São Paulo

Department of Basic Science Discipline of PharmacologyDiscipline of Pharmacology São Paulo State University (Unesp) School of Dentistry

Department of Restorative Dentistry Discipline of EndodonticsDiscipline of Endodontics São Paulo State University (Unesp) School of Dentistry

Department of Basic Science Discipline of PharmacologyDiscipline of Pharmacology São Paulo State University (Unesp) School of Dentistry

Tipo de Documento Artigo científico
Idioma Inglês
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