Department of Endodontology, Maurice and Gabriela Goldschleger School of Dental Medicine, Tel Aviv University, P.O. Box 39040, 6997801, Tel Aviv, Israel.
Clin Oral Investig. 2018 Jan;22(1):267-274. doi: 10.1007/s00784-017-2107-1. Epub 2017 Mar 28.
The purpose of this study was to evaluate Enterococcus faecalis colonization at the apical part of root canals following root-end resection and filling using confocal laser scanning microscopy (CLSM).
The apical 3-mm root-ends of 55 extracted single rooted human teeth were resected, and 3-mm retrograde cavities were prepared and filled using either mineral trioxide aggregate (MTA), intermediate restorative material (IRM), or Biodentine (n = 10 each); 25 teeth served as controls. The roots were placed in an experimental model, sterilized, and coronally filled with E. faecalis bacterial suspension for 21 days. Then, the apical 3-mm segments were cut to get two slabs (coronal and apical). The slabs were stained using LIVE/DEAD BacLight Bacterial Viability Kit and evaluated using CLSM.
The fluorescence-stained areas were larger in the bucco-lingual directions compared with the mesio-distal directions (p < 0.05). The mean and maximal depths of bacterial colonization into the dentinal tubules were 755 and 1643 μm, respectively, with no differences between the root-end filling materials (p > 0.05). However, more live bacteria were found in the MTA group in comparison to IRM and Biodentine groups (p < 0.05).
CLSM can be used to histologically demonstrate bacterial root-end colonization following root-end filling. This colonization at the filling-dentine interfaces and deeper into the dentinal tubules may be inhomogeneous, favoring the bucco-lingual aspects of the root.
Following root-end resection and filling bacterial colonization may lead to inflammatory reactions at the periapical tissues; the viability of the colonized bacteria may be affected by the type of root-end filling material.
本研究旨在通过共聚焦激光扫描显微镜(CLSM)评估根尖切除和填充后粪肠球菌在根管根尖部的定植情况。
从 55 颗单根人牙中切除根尖 3mm,使用矿物三氧化物聚合体(MTA)、中间修复材料(IRM)或 Biodentine 制备并填充 3mm 逆行腔(每组 n=10);25 颗牙作为对照。将根放入实验模型中,消毒,并用粪肠球菌细菌悬浮液进行 21 天的冠向填充。然后,切除根尖 3mm 段,获得两个薄片(冠向和根尖向)。使用 LIVE/DEAD BacLight 细菌活力试剂盒对薄片进行染色,并使用 CLSM 进行评估。
与近远中方向相比,颊舌方向的荧光染色区域更大(p<0.05)。细菌进入牙本质小管的平均和最大深度分别为 755 和 1643μm,根端填充材料之间无差异(p>0.05)。然而,与 IRM 和 Biodentine 组相比,MTA 组中发现更多的活菌(p<0.05)。
CLSM 可用于组织学上显示根端填充后细菌根端定植。这种在填充-牙本质界面和牙本质小管内更深部位的定植可能不均匀,有利于根的颊舌面。
根尖切除和填充后细菌定植可能导致根尖周组织的炎症反应;定植细菌的活力可能受根端填充材料的类型影响。