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低强度激光疗法对人牙髓干细胞活力的影响。

The Effect of Low-Level Laser Therapy on the Viability of Human Dental Pulp Stem Cells.

作者信息

Asnaashari Mohamad, Shojaeian Shiva, Mesgharani Ali, Mehrabinia Pegah

机构信息

Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Endodontics, Dental School, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

J Lasers Med Sci. 2022 Dec 8;13:e60. doi: 10.34172/jlms.2022.60. eCollection 2022.

Abstract

This study assessed the effect of low-level laser (LLL) irradiation on the viability of dental pulp stem cells (DPSCs). In this in vitro experimental study, human DPSCs were purchased from the cell bank of Iranian Genetic Resources and cultured in flasks containing Dulbecco's modified Eagle's medium supplemented with 20% fetal bovine serum (FBS) at 37°C, 5% CO2, and 95% humidity. The cells were stored in semi-confluent form, and the culture medium was refreshed every two days. The cells in the control group were not laser-irradiated, but the cells in the experimental groups were irradiated with 660-nm and 808-nm diode lasers with 4.1 J/cm energy density. Cell viability was assessed at baseline and after 24, 48, and 72 hours using the methyl thiazolyl tetrazolium (MTT) assay. The effects of laser irradiation, laser wavelength, and time on the percentage of cell viability were analyzed by two-way ANOVA and Tukey's test. The effects of laser irradiation and its wavelength (=0.04), time of assessment (<0.001), and the interaction effect of group and time (=0.02) on cell viability were significant. Cell viability in 660-nm and 808-nm laser groups at 48 and 72 hours was higher than that of the control group; however, only the difference in cell viability between the 660-nm laser group and the control group at 72 hours was statistically significant (=0.03). Considering the optimal effect of diode laser irradiation (particularly 660 nm) on the viability of DPSCs, we conclude that it may be suitable for relevant clinical applications.

摘要

本研究评估了低强度激光(LLL)照射对牙髓干细胞(DPSC)活力的影响。在这项体外实验研究中,从伊朗遗传资源细胞库购买人DPSC,并在含有补充20%胎牛血清(FBS)的杜尔贝科改良伊格尔培养基的培养瓶中,于37°C、5%二氧化碳和95%湿度条件下培养。细胞以半汇合形式保存,每两天更换一次培养基。对照组细胞未进行激光照射,而实验组细胞用能量密度为4.1 J/cm的660 nm和808 nm二极管激光照射。使用甲基噻唑基四氮唑(MTT)法在基线以及24、48和72小时后评估细胞活力。通过双向方差分析和图基检验分析激光照射、激光波长和时间对细胞活力百分比的影响。激光照射及其波长(=0.04)、评估时间(<0.001)以及组与时间的交互作用(=0.02)对细胞活力的影响具有显著性。660 nm和808 nm激光组在48和72小时时的细胞活力高于对照组;然而,仅660 nm激光组与对照组在72小时时的细胞活力差异具有统计学意义(=0.03)。考虑到二极管激光照射(特别是660 nm)对DPSC活力的最佳效果,我们得出结论,其可能适用于相关临床应用。

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