Department of Restorative Dentistry, Discipline of Endodontics, Dental School of Araraquara, São Paulo State University-UNESP, Rua Humaitá, 1680, PO 331, CEP 14.801-903, Araraquara, SP, Brazil.
Lasers Med Sci. 2011 Nov;26(6):741-7. doi: 10.1007/s10103-010-0797-6. Epub 2010 Jun 12.
Low-level laser therapy (LLLT) accelerates tissue repair. Mast cells induce the proliferation of fibroblasts and the development of local fibrosis. The objective of this study was to quantify fibrosis rate and mast cells in connective tissue after endodontic sealer zinc oxide and eugenol (ZOE) was implanted and submitted to LLLT, immediately after implant and again 24 h later. Sixty mice were distributed into three groups: GI, GII, and GIII (n = 20). In GI, the tubes filled with Endofill were implanted in the animals and were not irradiated with LLLT. In GII, the tubes containing Endofill were implanted in the animals and then irradiated with red LLLT (InGaAIP) 685-nm wavelength, D = 72 J/Cm(2), E = 2 J, T = 58 s, P = 35 mW, and in GIII, the tubes with Endofill were implanted and irradiated with infrared LLLT (AsGaAl) 830-nm wavelength, D = 70 J/Cm(2), E = 2 J, T = 40 s, P = 50 mW. After 7 days and 30 days, the animals were killed. A series of 6-µm-thick sections were obtained and stained with Toluidine Blue and Picrosirius and analyzed under a standard light microscope using a polarized light filter for the quantification of fibrosis. The statistics were qualitative and quantitative with a significance of 5%. The irradiation with LLLT did not offer improvement in the fibrosis rate, however, it provided a significant decrease in the concentration of independent mast cells for the period studied.
低水平激光疗法(LLLT)可加速组织修复。肥大细胞诱导成纤维细胞增殖和局部纤维化的发展。本研究的目的是量化根管封闭剂氧化锌丁香酚(ZOE)植入后,经 LLLT 即刻和 24 小时后,在结缔组织中的纤维化率和肥大细胞。60 只小鼠随机分为三组:GI、GII 和 GIII(n = 20)。在 GI 组,将充满 Endofill 的管植入动物体内,并用 LLLT 照射。在 GII 组,将含有 Endofill 的管植入动物体内,然后用红色 LLLT(InGaAIP)685nm 波长照射,D = 72J/Cm(2),E = 2J,T = 58s,P = 35mW;在 GIII 组,将含有 Endofill 的管植入并用红外 LLLT(AsGaAl)830nm 波长照射,D = 70J/Cm(2),E = 2J,T = 40s,P = 50mW。7 天后和 30 天后处死动物。获得一系列 6μm 厚的切片,用甲苯胺蓝和苦味酸染色,并在标准光显微镜下用偏光滤光片分析,以定量纤维化。统计学采用定性和定量分析,显著性水平为 5%。LLLT 照射并未提高纤维化率,但在研究期间显著降低了独立肥大细胞的浓度。