Vijaykumar Sagare Shweta, Patil Anand, Patıl Pranav, Kumar R Susheel, Gangishetti Sairam, Ingale Priya
Department of Conservative Dentistry and Endodontics, Bharati Vidyapeeth (Deemed To Be University) Dental College and Hospital, Sangli, IND.
Department of Conservative Dentistry and Endodontics, KLE Vishwanath Katti Institute of Dental Sciences and Hospital, KLE Academy of Higher Education and Research, Belagavi, IND.
Cureus. 2023 Mar 29;15(3):e36837. doi: 10.7759/cureus.36837. eCollection 2023 Mar.
Aim This study aimed to evaluate the protective effects of extract and juice on human periodontal ligament (PDL) cells after the reimplantation of avulsed teeth using a collagenase-dispase test. Materials and methods Sixty-five human premolars, all of which would eventually need to be extracted, were split into three experimental groups: one treated with Hanks Balanced Salt Solution, another with Morinda citrifolia juice and Ocimum sanctum extract, and two control groups (positive and negative).There were 10 teeth in each control group and 15 teeth each were used in the experimental groups, with the first 30 minutes spent dry before being submerged in one of three experimental media for 45 minutes, followed by 30 minutes of treatment with collagenase and dispase II. The cells' vitality was measured by the trypsin dye exclusion technique. To determine how many PDL cells were still alive, An optical microscope and a hemocytometer were used. The data were analyzed using Kruskal-Wallis one-way ANOVA and Mann-Whitney U tests. Results The percentage of viable PDL cells was greatest in juice (85.18%), followed by HBSS (84.3%), and finally by extract (68.04%). There was no significant difference in the number of viable PDL cells in juice and HBSS. Conclusion The results of this research suggest that juice has potential as a storage medium and as an alternative to HBSS, within the study's constraints, considering its availability as well as economic feasibility.
目的 本研究旨在通过胶原酶- dispase试验评估阿育吠陀草药提取物和诺丽果汁对脱位牙再植后人牙周膜(PDL)细胞的保护作用。材料与方法 65颗最终均需拔除的人类前磨牙被分为三个实验组:一组用汉克斯平衡盐溶液处理,另一组用诺丽果汁和神圣罗勒提取物处理,还有两个对照组(阳性和阴性)。每个对照组有10颗牙,实验组每组各用15颗牙,在浸入三种实验培养基之一前先干燥30分钟,然后在其中浸泡45分钟,接着用胶原酶和dispase II处理30分钟。通过胰蛋白酶染料排除技术测量细胞活力。使用光学显微镜和血细胞计数器来确定仍存活的PDL细胞数量。数据采用Kruskal-Wallis单因素方差分析和Mann-Whitney U检验进行分析。结果 诺丽果汁中存活的PDL细胞百分比最高(85.18%),其次是汉克斯平衡盐溶液(84.3%),最后是神圣罗勒提取物(68.04%)。诺丽果汁和汉克斯平衡盐溶液中存活的PDL细胞数量无显著差异。结论 本研究结果表明,在本研究的限制范围内,考虑到诺丽果汁的可得性以及经济可行性,诺丽果汁有作为储存介质和替代汉克斯平衡盐溶液的潜力。