Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla 9-75, Bauru, SP, 17012-901, Brazil.
Lasers Med Sci. 2021 Apr;36(3):541-553. doi: 10.1007/s10103-020-03056-5. Epub 2020 Jun 8.
The purposes of this study are to evaluate the effects of photobiomodulation (PBM) with laser and LED on rat calvaria osteoblasts (rGO lineage), cultured in osteogenic (OST) or regular (REG) medium, after induction of a quiescent state and to test if PBM is capable of osteogenic induction and if there is a sum of effects when combining OST medium with PBM. Before irradiation, the cells were put in a quiescent state (1% FBS) 24 h, when red (AlGaInP-660 nm) and infrared laser (GaAlAs-808 nm) and LED (637 ± 15 nm) were applied. The groups were as follows: red laser (RL3-5 J/cm, 3 s and RL5-8.3 J/cm, 5 s, 1.66 W/cm); infrared laser (IrL3-5 J/cm, 3 s and IrL5-8.3 J/cm, 5 s); LED (LED3-3 s and LED5-5 s, 0.02 J/cm, 0.885 W/cm); positive (C+, 10% FBS) and negative control (C-, 1% FBS). For alkaline phosphatase (ALP) and mineralization assays, the cells were cultured in REG (DMEM 10% FBS) and OST medium (DMEM 10% FBS, 50 μg/mL ascorbic acid, 10 mM β-glycerophosphate). Statistical analysis was performed using ANOVA and Tukey's tests (p < 0.05). RL5 and LED5 increased proliferation, in vitro wound closure, ALP, and mineralization in rGO cells (p < 0.05). PBM with red laser and LED induced mineralization by itself, without osteogenic medium, not observed for infrared laser (p < 0.05). A sum of effects was observed in osteogenic medium and PBM by infrared, red laser, and LED (5 s). Red laser and LED increased proliferation, migration, and secretory phases in rGO cells in a dose-dependent manner. PBM with red laser and LED promotes osteogenic induction by itself. PBM with infrared laser and osteogenic medium potentializes mineralization.
本研究旨在评估光生物调节(PBM)对激光和 LED 照射静止状态下培养于成骨(OST)或常规(REG)培养基中的大鼠颅骨成骨细胞(rGO 系)的影响,并测试 PBM 是否具有成骨诱导能力,以及将 OST 培养基与 PBM 联合使用是否会产生累加效应。照射前,细胞在静止状态下(1% FBS)孵育 24 小时,然后施加红光(AlGaInP-660nm)和红外激光(GaAlAs-808nm)和 LED(637±15nm)。分组如下:红光激光(RL3-5J/cm,3s 和 RL5-8.3J/cm,5s,1.66W/cm);红外激光(IrL3-5J/cm,3s 和 IrL5-8.3J/cm,5s);LED(LED3-3s 和 LED5-5s,0.02J/cm,0.885W/cm);阳性对照(C+,10% FBS)和阴性对照(C-,1% FBS)。用于碱性磷酸酶(ALP)和矿化测定的细胞在 REG(DMEM 10% FBS)和 OST 培养基(DMEM 10% FBS、50μg/mL 抗坏血酸、10mM β-甘油磷酸)中培养。使用方差分析和 Tukey 检验进行统计学分析(p<0.05)。RL5 和 LED5 增加了 rGO 细胞的增殖、体外伤口闭合、ALP 和矿化(p<0.05)。PBM 用红光激光和 LED 诱导矿化本身,而无需成骨培养基,而红外激光则没有观察到(p<0.05)。在成骨培养基和 PBM 中观察到了红外、红光激光和 LED 的累加效应(5s)。红光激光和 LED 以剂量依赖的方式增加 rGO 细胞的增殖、迁移和分泌阶段。PBM 用红光激光和 LED 本身可促进成骨诱导。PBM 用红外激光和成骨培养基可增强矿化。