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低强度砷化镓铝激光照射对人牙周膜成纤维细胞增殖率的影响:一项体外研究。

Effect of low-level GaAlAs laser irradiation on the proliferation rate of human periodontal ligament fibroblasts: an in vitro study.

作者信息

Kreisler Matthias, Christoffers Ann B, Willershausen Britta, d'Hoedt Bernd

机构信息

Department of Oral Surgery, Johannes Gutenberg-University, Augustusplatz 2, 55131 Mainz, Germany.

出版信息

J Clin Periodontol. 2003 Apr;30(4):353-8. doi: 10.1034/j.1600-051x.2003.00001.x.

Abstract

AIM

The aim of this in vitro study was to evaluate a potential stimulatory effect of low-level laser irradiation on the proliferation of human periodontal ligament fibroblasts (PDLF).

MATERIALS AND METHODS

PDLF obtained from third molar periodontal ligaments were cultured under standard conditions and spread on 96-well tissue culture plates. Subconfluent monolayers were irradiated with an 809-nm diode laser operated at a power output of 10 mW in the continuous wave (cw) mode at energy fluences of 1.96-7.84 Jcm-2. The variable irradiation parameters were the time of exposure (75-300 s per well) and the number of irradiations (1-3). After laser treatment, the cultures were incubated for 24 h. The proliferation rate of the lased and control cultures was determined by means of fluorescence activity of a reduction-oxidation (REDOX) indicator (Alamar Blue Assay) added to the cell culture. Proliferation, expressed in relative fluorescence units (RFU), was determined 24, 48 and 72 h after irradiation.

RESULTS

The irradiated cells revealed a considerably higher proliferation activity than the controls. The differences were significant up to 72 h after irradiation (Mann-Whitney U-test, p<0.05).

CONCLUSION

A cellular effect of the soft laser application is clearly discernible. Clinical studies are needed to evaluate whether the application of low-level laser therapy might be beneficial in regenerative periodontal therapy.

摘要

目的

本体外研究旨在评估低强度激光照射对人牙周膜成纤维细胞(PDLF)增殖的潜在刺激作用。

材料与方法

从第三磨牙牙周膜获取的PDLF在标准条件下培养,并铺于96孔组织培养板上。用809纳米二极管激光以连续波(cw)模式、10毫瓦的输出功率、1.96 - 7.84焦/平方厘米的能量通量照射亚汇合单层细胞。可变的照射参数为照射时间(每孔75 - 300秒)和照射次数(1 - 3次)。激光处理后,将培养物孵育24小时。通过向细胞培养物中添加还原 - 氧化(REDOX)指示剂(alamar蓝测定法)的荧光活性来测定激光照射组和对照组培养物的增殖率。在照射后24、48和72小时测定以相对荧光单位(RFU)表示的增殖情况。

结果

照射后的细胞显示出比对照组明显更高的增殖活性。照射后72小时内差异显著(曼 - 惠特尼U检验,p < 0.05)。

结论

软激光应用的细胞效应清晰可见。需要进行临床研究以评估低强度激光治疗在牙周再生治疗中是否有益。

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