Gorduysus Melahat, Avcu Nihal, Gorduysus Omer, Pekel Aysel, Baran Yusuf, Avcu Ferit, Ural Ali Ugur
Department of Endodontics, Hacettepe University, Ankara, Turkey.
J Endod. 2007 Dec;33(12):1450-4. doi: 10.1016/j.joen.2007.08.017. Epub 2007 Oct 22.
The purpose of this study was to compare the cytotoxicity, induced apoptosis and/or necrosis, and apoptotic mechanisms in human periodontal ligament (PDL) fibroblasts treated with four different endodontic materials: White ProRoot mineral trioxide aggregate (MTA) (MTA/Dentsply; Tulsa Dental, Memphis, TN), Diaket (ESPE, Seefeld, Germany), Endion (VOCO, Cuxhaven, Germany), and CYMED 8410 (NANO, Kaohsiung, Taiwan). The effects of these four materials on the viability of PDL fibroblasts were determined by MTT (3-(4,5-dimethyl-thiazoyl)-2,5-diphenyl-SH-tetrazolium bromide) assay. Apoptotic pathways were evaluated via several mechanisms. Exposure to MTA for 24, 48, and 72 hours resulted in no significant differences in MTT reduction and viable cell number compared with controls. However, treatment of PDL fibroblasts with Diaket, Endion, and CYMED 8410 for 24, 48, and 72 hours resulted in cytotoxicity with MTT and a reduction of viable cell number with trypan blue dye exclusion test compared with controls (from p < 0.05 to p < 0.001). Annexin V-FITC/PI staining showed that Diaket, Endion, and CYMED 8410 induced higher percentages of apoptosis and/or necrosis than in controls (45.6%, 25.5%, and 6.3%, respectively). Results of cell-cycle analyses were concordant with annexin V-FITC/PI staining findings. These results suggest that MTA is a very biocompatible filling material. However, Diaket, Endion, and CYMED 8410 are toxic to PDL fibroblasts in vitro. The main form of cell death induced by these filling materials was determined to be apoptosis and/or necrosis.
本研究的目的是比较用四种不同的根管治疗材料处理的人牙周膜(PDL)成纤维细胞的细胞毒性、诱导的凋亡和/或坏死以及凋亡机制:白色ProRoot三氧化矿物凝聚体(MTA)(MTA/登士柏;塔尔萨牙科,田纳西州孟菲斯)、Diaket(贺利氏古莎,德国塞费尔德)、Endion(VOCO,德国库克斯港)和CYMED 8410(纳米,台湾高雄)。通过MTT(3-(4,5-二甲基噻唑基)-2,5-二苯基-SH-溴化四氮唑)试验测定这四种材料对PDL成纤维细胞活力的影响。通过多种机制评估凋亡途径。与对照组相比,暴露于MTA 24、48和72小时导致MTT还原和活细胞数量无显著差异。然而,用Diaket、Endion和CYMED 8410处理PDL成纤维细胞24、48和72小时,与对照组相比,MTT检测显示细胞毒性,台盼蓝染料排除试验显示活细胞数量减少(从p<0.05至p<0.001)。膜联蛋白V-FITC/PI染色显示,Diaket、Endion和CYMED 8410诱导的凋亡和/或坏死百分比高于对照组(分别为45.6%、25.5%和6.3%)。细胞周期分析结果与膜联蛋白V-FITC/PI染色结果一致。这些结果表明,MTA是一种生物相容性非常好的填充材料。然而,Diaket、Endion和CYMED 8410在体外对PDL成纤维细胞有毒性。这些填充材料诱导的细胞死亡主要形式被确定为凋亡和/或坏死。