Clinic of Operative Dentistry, Medical Faculty Carl Gustav Carus, TU Dresden, Fetscherstr.74, 01307, Dresden, Germany.
Vertriebsgesellschaft GmbH, Geistlich Biomaterials, Schneidweg 5, 76534, Baden-Baden, Germany.
Clin Oral Investig. 2019 Dec;23(12):4325-4334. doi: 10.1007/s00784-019-02865-5. Epub 2019 Mar 19.
The aim of the present vitro study was to examine the question whether devitalized Enterococcus faecalis (E. faecalis) cells can migrate into dentinal tubules and if that process takes place in a time-dependent manner.
Sixty bovine root canals were incubated with devitalized and vital streptomycin-resistant E. faecalis strains after root canal enlargement (size 80, taper .02) with 3% NaOCl solution. Incubation times 7, 14, 21, 28, 35, and 42 days. Samples were processed for analysis by scanning electron microscopy (SEM) and DAPI (4',6-diamidino-2-phenylindole) staining. The penetration depth was calculated with the measurement tool of the Axio Vision program (Zeiss, Jena, Germany). Statistical analysis was performed by Kruskal-Wallis (α = 0.05) and Mann-Whitney U test (p < 0.05).
Devitalized E. faecalis strains were able to migrate into dentinal tubules. The total number and penetration depth of devitalized E. faecalis cells was lower compared to the vital suspension of E. faecalis. It was noted, that bacterial penetration was not common to all of the dentinal tubules in the vital E. faecalis control and especially in the devitalized control. The migration took place in a time-dependent migration characteristic.
Devitalized E. faecalis cells are still able to migrate into the dentinal tubules due to possible electrokinetic and osmotic processes. Thereby, increased exposure times lead to a time-dependent penetration characteristic.
Since devitalized bacteria can migrate as well into dentinal tubules, the presence of bacteria within dentinal tubules cannot be interpreted as a failure of tested preparation regimens.
本体外研究旨在探讨失活粪肠球菌(E. faecalis)细胞是否能够迁移到牙本质小管中,以及该过程是否具有时间依赖性。
用 3%次氯酸钠溶液对 60 个牛牙根进行根管扩大(尺寸 80,锥度.02)后,将失活和有活力的链霉素耐药粪肠球菌菌株与失活和有活力的粪肠球菌菌株孵育。孵育时间分别为 7、14、21、28、35 和 42 天。通过扫描电子显微镜(SEM)和 DAPI(4',6-二脒基-2-苯基吲哚)染色对样本进行分析。使用 Axio Vision 程序(蔡司,耶拿,德国)的测量工具计算穿透深度。通过 Kruskal-Wallis(α=0.05)和 Mann-Whitney U 检验(p<0.05)进行统计分析。
失活的粪肠球菌菌株能够迁移到牙本质小管中。与有活力的粪肠球菌悬浮液相比,失活粪肠球菌菌株的总数和穿透深度较低。值得注意的是,在有活力的粪肠球菌对照组和失活对照组中,并非所有牙本质小管都存在细菌穿透,特别是失活对照组。这种迁移具有时间依赖性的迁移特征。
由于可能存在电动和渗透过程,失活的粪肠球菌细胞仍能够迁移到牙本质小管中。因此,增加暴露时间会导致时间依赖性穿透特征。
由于失活的细菌也可以迁移到牙本质小管中,因此牙本质小管内存在细菌不能被解释为测试的预备方案失败。