Stähli Alexandra, Feuz Sarah, Jutzi Anja Elisabeth, Berto Luciana Pisenti, Nietzsche Sandor, Sculean Anton, Eick Sigrun
Department of Periodontology, School of Dental Medicine, University of Bern, Bern, Switzerland.
Department of Restorative, Preventive and Pediatric Dentistry, School of Dental Medicine, University of Bern, Bern, Switzerland.
Clin Oral Investig. 2025 Apr 24;29(5):268. doi: 10.1007/s00784-025-06321-5.
To investigate in vitro the influence of instrumentation methods on the bacterial colonization of root dentine and pulpal cell behaviour seeded into the pulp cavum.
Extracted teeth underwent root canal treatment with sealing of apices. The teeth were subjected to periodontal instrumentation using manual, ultrasonic scalers, air polishing, or left untreated. The root surfaces were then incubated with a mixture of six bacterial species for 2 h, 24 h and 10 weeks, before dentine samples were taken and analyzed for bacterial colony forming units (cfu) counts. In an additional series, pulpal cells were seeded into the reopened pulp chambers after 10 weeks of incubation with the bacterial mixture and analysed for interleukin (IL)-8 and matrix metalloprotease (MMP)-3 expression.
After 2 and 24 h of incubation, instrumented dentine samples contained fewer bacteria than the controls (median (log10 cfu): 5.73 vs. 5.92; 7.71 vs. 8.01 (p = 0.007; p = 0.017)). At 24 h, among the instrumentation groups the highest cfu counts were observed in the ultrasonic group (p = 0.012 vs. manual scaler group; p = 0.002 vs. air polishing group). After 10 weeks, the number of viable bacteria (cfu) decreased in all groups with no difference between any group. Pulpal cells seeded in teeth, with or without prior instrumentation, but exposed to the bacterial mixture for 10 weeks, released higher levels of IL-8 and MMP-3 compared to those in uncontaminated and untreated controls.
Instrumentation initially inhibits bacterial colonisation. Prolonged exposure of the outer root surface to bacteria may increase the inflammatory response of pulpal cells.
Regular removal of bacteria from the root surface is supported by these in vitro data.
在体外研究器械操作方法对牙根牙本质细菌定植以及接种到髓腔中的牙髓细胞行为的影响。
对拔除的牙齿进行根管治疗并封闭根尖。使用手动器械、超声洁牙器、空气抛光对牙齿进行牙周器械操作,或不进行处理。然后将牙根表面与六种细菌的混合物孵育2小时、24小时和10周,之后采集牙本质样本并分析细菌集落形成单位(cfu)计数。在另一个系列中,在与细菌混合物孵育10周后,将牙髓细胞接种到重新打开的髓腔中,并分析白细胞介素(IL)-8和基质金属蛋白酶(MMP)-3的表达。
孵育2小时和24小时后,经过器械操作的牙本质样本中的细菌数量少于对照组(中位数(log10 cfu):5.73对5.92;7.71对8.01(p = 0.007;p = 0.017))。在24小时时,在器械操作组中,超声组的cfu计数最高(与手动器械组相比,p = 0.012;与空气抛光组相比,p = 0.002)。10周后,所有组中的活菌数量(cfu)均减少,各组之间无差异。与未受污染且未处理的对照组相比,接种到牙齿中的牙髓细胞,无论是否预先进行器械操作,但暴露于细菌混合物10周后,释放出更高水平的IL-8和MMP-3。
器械操作最初会抑制细菌定植。牙根外表面长期暴露于细菌可能会增加牙髓细胞的炎症反应。
这些体外数据支持定期从牙根表面清除细菌。