Ozan Fatih, Polat Zübeyde Akin, Tepe Bektaş, Er Kürşat
Department of Oral and Maxillofacial Surgery, Cumhuriyet University, Sivas, Turkey.
J Contemp Dent Pract. 2008 Sep 1;9(6):17-24.
The purpose of this study was to determine the ability of Salvia officinalis (S. officinalis) extracts to serve as a storage medium for the maintenance of periodontal ligament (PDL) cell viability of avulsed teeth.
PDL cells were obtained from healthy third molars and cultured in Dulbecco's Modi?ed Eagle's Medium (DMEM). Cultures were subjected to 4, 2.5, 1.5, and 0.5% S. officinalis solutions, Hank's balanced salt solution (HBSS), phosphate buffered saline (PBS), and tap water. Tissue culture plates were incubated with experimental media at 37 masculineC for 1, 3, 6, 12 or 24 hours. PDL cell viability was assessed by trypan blue exclusion. Statistical analysis of the data was performed by one-way analysis of variance (ANOVA) complemented by the Tukey's test. The level of significance was 5% (p< 0.05).
The results showed 2.5% S. officinalis was a more effective storage medium than the other experimental solutions (p<0.05). Only at 1 hour and 3 hours was there found similar effect between 2.5% S. officinalis and HBSS. At 24 hours, 2.5% S. officinalis was found to be significantly better than the other solutions tested.
S. officinalis can be recommended as a suitable transport medium for avulsed teeth.
The findings of this study support the use of S. officinalis as another option for clinicians to use to store and transport avulsed teeth until reimplantation procedures can be done.
本研究旨在确定鼠尾草提取物作为储存介质维持离体牙牙周膜(PDL)细胞活力的能力。
从健康的第三磨牙获取PDL细胞,并在杜氏改良 Eagle 培养基(DMEM)中培养。培养物分别置于4%、2.5%、1.5%和0.5%的鼠尾草溶液、汉克平衡盐溶液(HBSS)、磷酸盐缓冲盐水(PBS)和自来水中。将组织培养板与实验培养基在37℃孵育1、3、6、12或24小时。通过台盼蓝排斥法评估PDL细胞活力。数据的统计分析采用单因素方差分析(ANOVA)并辅以 Tukey 检验。显著性水平为5%(p<0.05)。
结果表明,2.5%的鼠尾草溶液是比其他实验溶液更有效的储存介质(p<0.05)。仅在1小时和3小时时,发现2.5%的鼠尾草溶液与HBSS之间有相似的效果。在24小时时,发现2.5%的鼠尾草溶液明显优于其他测试溶液。
鼠尾草可被推荐为离体牙合适的运输介质。
本研究结果支持将鼠尾草作为临床医生在进行再植手术前储存和运输离体牙的另一种选择。