Abstract

The present study aimed to evaluate in vitro whether the low-level laser (LLL) delivering fractionated total energy (multiple irradiation) or single irradiation stimulates regeneration-associated events (viability and proliferation) in stem cells from human exfoliated deciduous teeth (SHED). Cells received LLL irradiation (InGaAlP-660nm), according to the following experimental groups: G1 (single irradiation 2.5J/cm2, 10mW, 10s, 0.10J), G2 (single irradiation 5.0J/cm2, 10mW, 20s, 0.20J), G3 (single irradiation 7.5J/cm2, 10mW, 30s, 0.30J), G4 (twoirradiations 2.5J/cm2, 10mW, 10s; total energy 0.20J), G5 (threeirradiations 2.5J/cm2, 10mW, 10s; total energy 0.30J), and G6 (non-irradiated). Cell viability was assessed by MTT and trypan blue exclusion (TBE) methods, while cell proliferation was evaluated by crystal violet (CV) and sulforhodamine B (SRB) assays after 24, 48, and 72h after the first irradiation. By MTT, there was no difference between groups at 24 and 72h. At 48h, the groups subjected to multiple irradiation (G4 and G5) presented higher cell viability rates. The average percentages of viable cells for all groups by TBE method were 91.04%, 96.63%, and 97.48% at 24, 48, and 72h, respectively. By CV, there was no significant difference between groups at 24 and 48h; at 72h, G2, G3, and G4 presented higher cell proliferation. By SRB, G1 and G4 presented lower proliferation rates in all the periods. When the groups presenting the same total energy were compared, G2 (0.20J) presented lower cell viability rates and higher cell proliferation rates in comparison with G4; G3 (0.30J) presented similar results to those of G5, with higher cell viability and proliferation. The application of laser delivering fractionated total energy (two or three applications of 2.5J/cm2) induced higher cell viability at 48h, while the single irradiation with 2.5J/cm2 did not stimulate metabolic activity in such period and the proliferation over time. The 5.0 and 7.5J/cm2 single doses and the threeapplications of 2.5J/cm2 maintained cell viability and stimulated proliferation of SHED at 72h.

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