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Low-Level Laser Effects on Simulated Orthodontic Tension Side Periodontal Ligament Cells

机译:低水平激光对正畸张力侧牙周膜细胞的影响

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摘要

>Objective: The purpose of this study was to analyze proliferation, inflammation, and osteogenic effects on periodontal ligament (PDL) cells after low-level laser therapy (LLLT) under simulated orthodontic tension conditions. >Background data: Low-level lasers affect fibroblast proliferation and collagen synthesis and reduce inflammation. Few studies have focused on the LLLT changes in the PDL caused by moving teeth. >Materials and methods: A human PDL cell line was cultured in a −100 kPa tension incubator. The PDL cells were treated with a 670 nm low-level diode laser, output power of 500 mW (continuous wave modus) for 2.5 or 5 sec, spot area 0.25 cm2, corresponding to 1.25 and 2.5 J at an energy density of 5 or 10 J/cm2, respectively. PDL cell viability was assayed by detecting the ability of the cells to cleave tetrazolium salt to formazan dye. Inflammation and osteogenic markers were analyzed by Western blot analysis. >Results: PDL cell viablity increased in the experimental group, based on the ability of the cells to cleave tetrazolium salt at day 7 (p<0.05). The experimental group showed no difference in PDL cellular morphology compared with the control group. The inflammation markers inducible NO synthase (iNOS), cyclooxygenase (COX)-2 and interleukin (IL)-1 showed stronger expression in 5 and 10 J/cm2 therapy at days 1 and 5, but decreased in expression at day 7. The osteogenic marker osteocalcin (OC) expression level was significantly higher at day 7 (p<0.05) than in the control cells. >Conclusions: LLLT significantly increased PDL cell proliferation, decreased PDL cell inflammation, and increased PDL OC activity under the tension conditions used in this study.
机译:>目的:本研究的目的是分析在模拟正畸张力条件下低水平激光治疗(LLLT)后对牙周膜(PDL)细胞的增殖,炎症和成骨作用。 >背景数据:低强度激光会影响成纤维细胞增殖和胶原蛋白合成并减少炎症。很少有研究关注因牙齿移动而引起的PDL的LLLT变化。 >材料和方法:将人PDL细胞系在−100 kPa张力培养箱中培养。用670 withnm的低级二极管激光器对PDL电池进行处理,输出功率为500 mW(连续波模式),持续2.5或5 sec,光斑面积为0.25 cm 2 ,分别为1.25和2.5 J能量密度分别为5或10 J / cm 2 。通过检测细胞将四唑盐裂解为甲for染料的能力来测定PDL细胞的活力。通过蛋白质印迹分析分析炎症和成骨标记。 >结果:基于第7天细胞裂解四唑盐的能力,实验组的PDL细胞存活率增加(p <0.05)。实验组与对照组相比,PDL细胞形态无差异。炎症标志物诱导型一氧化氮合酶(iNOS),环氧合酶(COX)-2和白介素(IL)-1在第1天和第5天的5和10 J / cm 2 治疗中表现出较强的表达,但下降在第7天的表达中成骨标志物骨钙素(OC)的表达水平在第7天时显着高于对照细胞(p <0.05)。 >结论:在这项研究中使用的张力条件下,LLLT显着增加了PDL细胞的增殖,减少了PDL细胞的炎症,并增加了PDL OC的活性。

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