Background. The growth and proliferation of gingival fibroblasts are important in the process of oral wound healing, and photobiomodulation (PBM) might be able to modify this process. Objectives. The aim of the current study was to evaluate the biomodulatory effect of a single session of laser PBM by means of 810 nm and 940 nm diode lasers alone and their combined application with different fluencies on human gingival fibroblasts (HGFs). Material and methods. Cells were provided by the Pasteur Institute, the National Cell Bank of Iran (NCBI) (C-165). Laser irradiation was carried out using 810 nm, 940 nm and 810 nm + 940 nm in the continuous wave (CW) mode, 100 mW, and energy densities of 0.5, 1.5 and 2.5 J/cm(2). Cell viability was evaluated at 24 h with the MTT assay. Trypan blue staining was used to evaluate proliferation 24, 48 and 72 h after laser therapy. Propidium iodine was used to stain DNA and the cell nucleus. Results. Laser irradiation (810 nm, 0.5 J/cm(2)) increased the viability of gingival fibroblasts, while this dose had an inhibitory effect with 940 nm. No positive effect on cell viability was found with other settings at 24 h. The viability results were not statistically different from those of the control in the dual wavelength group. At all single-laser irradiation doses, the cell proliferation results were lower as compared to the control at 48 and 72 h. The dual wavelength group results were significantly better than those of the control for the 1.5 J/cm(2) and 2.5 J/cm(2) energy densities (p < 0.001). Propidium iodine staining showed no negative effect of laser irradiation on the cell nucleus in any of the groups. Conclusions. Although a single irradiation dose of 810 nm, 0.5 J/cm(2), resulted in a positive effect on cell viability at 24 h, no statistically significant stimulatory effect on viability and proliferation was observed for the other single wavelength group. When a combination of the 2 wavelengths was used, better results were observed as compared to the control, which needs to be further investigated in future studies.

Introduction: The final goal of root canal therapy is to remove of the most bacteria from the root canal. This study aimed at comparing the antibacterial effects of a diode laser with a wavelength of 940nm and silver nanoparticles and the synergic effects of both techniques on Enterococcus faecalis. Methods: Ninety single-rooted human teeth were decoronated and prepared with rotary files. The samples were irrigated with sodium hypochlorite and EDTA17%. Then they were autoclaved and contaminated with E. faecalis suspension (1.5 × 108 CFU/mL) for 21 days. The samples were fixed in a microtube and were randomly divided into 4 experimental (n=20) groups and a negative control group (n=10) as follows: Group 1: hypochlorite sodium 5%, Group 2: silver nanoparticle, Group 3: diode laser, and Group 4: diode laser and silver nanoparticle. The samples were obtained from dentin chips before and after the intervention. The data were analysed using the Kruskal-Wallis nonparametric test. Furthermore, alterations in bacterial colonies were entered using the Wilcoxon signed ranks test (α=0.05). Results: There was a significant decrease in colony counts for all groups after interventions (P value<0.05). Also, all groups showed more reductions in colony counts compared with the negative control group (P value <0.004). There was a significant reduction for group 1 in comparison with other groups (P value <0.001) and this group had an extreme decrease of colony counts (RCC=100%). There was an important differential between silver nanoparticles and diode laser groups in bacterial counts (P value<0.001) and silver nanoparticles (RCC=83.15%) had more efficiency than the diode laser (RCC=41/33%). RCC of group 4 was 68/52%. Conclusion: Followed by sodium hypochlorite 5%, silver nanoparticles were the most effective antibacterial substances. The 940 nm laser diode had less antibacterial effect compared to its use with silver nanoparticles.

Background and Aim: Dental caries is a communicable and the most prevalent infectious disease worldwide. Salivary oxidative stress and antioxidants may play a pivotal role in caries prevention, progression and pathogenesis. In this study, salivary superoxide dismutase, peroxidase, glutathione peroxidase, catalase and uric acid levels were evaluated in dental caries. Material and Method: One hundred male and female students in two groups (n=50) were subdivided into caries-active and caries-free (25) groups. Whole saliva samples were collected in the morning, and the salivary antioxidant levels were measured by a spectrophotometric assay. The data were analyzed using SPSS. Results: The caries-active group had higher peroxidase, uric acid, catalase and glutathione peroxidase levels, and lower superoxide dismutase level as compared to the caries-free group. The comparison between males and females showed lower peroxidase, catalase and uric acid levels and higher glutathione peroxidase levels in the female group. Conclusion: The caries-active group had altered salivary antioxidant levels. Therefore, it was concluded that salivary antioxidants have significant effects on oral and dental health.

This in vitro study compared the apical sealing ability of three common root end filling materials namely mineral trioxide aggregate (MTA), intermediate restorative material (IRM) and calcium-enriched mixture (CEM) cement using a bacterial leakage model. The study was conducted on 83 single-rooted human teeth. Tooth crowns were cut and root canals were prepared using the step-back technique. Apical 3 mm of the roots were cut and a three-mm-deep cavity was prepared using an ultrasonic instrument. The samples were divided into three groups (n=25) according to the root-end filling material including MTA, IRM and CEM cement. The roots were inserted into cut-end microtubes. After sterilization with ethylene oxide, microtubes were placed in sterile vials containing 10 mL of Brain Heart Infusion (BHI) broth and incubated at 37°C and 0.1 mL of Enterococcus faecalis suspension compatible with 0.5 McFarland standard (1.5×108 cell/ ml), which was refreshed daily. This procedure was continued for 70 days. The data were analyzed using the chi-square, Kruskal-Wallis and log rank tests. The level of significance was set at 0.05. No significant difference was found in bacterial microleakage among three groups; MTA showed slightly (but not significantly) less microleakage than IRM and CEM. However, the difference in the mean time of microleakage was significant among the groups (P<0.04) and in MTA samples leakage occurred in a longer time than CEM (P<0.012). The three tested root end filling materials had equal sealing efficacy for preventing bacterial leakage.