Kaku Masato, Sumi Hiromi, Shikata Hanaka, Kojima Shunichi, Motokawa Masahide, Fujita Tadashi, Tanimoto Kotaro, Tanne Kazuo
Department of Orthodontics and Craniofacial Developmental Biology, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan.
Department of Orthodontics and Craniofacial Developmental Biology, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan.
J Endod. 2014 Mar;40(3):372-8. doi: 10.1016/j.joen.2013.11.027. Epub 2014 Jan 8.
Previous studies have revealed that orthodontic force affects dental pulp via the rupture of blood vessels and vacuolization of pulp tissues. We hypothesized that pulp tissues express inflammatory cytokines and regulators of odontoclast differentiation after excess orthodontic force. The purpose of this study was to investigate the effects of tensile force in human pulp cells and to measure inflammatory root resorption during tooth movement in pulpless rat teeth.
After cyclic tensile force application in human pulp cells, gene expression and protein concentration of macrophage colony-stimulating factor, receptor activator of nuclear factor kappa-B ligand, interleukin-1 beta, and tumor necrosis factor alpha were determined by real-time polymerase chain reaction and enzyme-linked immunoassay. Moreover, the role of the stretch-activated channel was evaluated by gadolinium (Gd(3+)) treatment. The upper right first molars of 7-week Wistar rats were subjected to pulpectomy and root canal filling followed by mesial movement for 6 months.
The expression of cytokine messenger RNAs and proteins in the experimental group peaked with loading at 10-kPa tensile force after 48 hours (P < .01). Gd(3+) reduced the expression of these cytokine messenger RNAs and protein concentrations (P < .01). The amount of inflammatory root resorption was significantly larger in the control teeth than the pulpectomized teeth (P < .05).
This study shows that tensile forces in the pulp cells enhance the expression of various cytokines via the S-A channel, which may lead to inflammatory root resorption during tooth movement. It also suggests that root canal treatment is effective for progressive severe inflammatory root resorption during tooth movement.
先前的研究表明,正畸力通过血管破裂和牙髓组织空泡化影响牙髓。我们推测,正畸力过大后,牙髓组织会表达炎性细胞因子和破骨细胞分化调节因子。本研究的目的是研究拉伸力对人牙髓细胞的影响,并测量无牙髓大鼠牙齿移动过程中的炎性牙根吸收情况。
对人牙髓细胞施加周期性拉伸力后,通过实时聚合酶链反应和酶联免疫吸附测定法测定巨噬细胞集落刺激因子、核因子κB受体激活剂配体、白细胞介素-1β和肿瘤坏死因子α的基因表达和蛋白浓度。此外,通过钆(Gd(3+))处理评估牵张激活通道的作用。对7周龄Wistar大鼠的右上第一磨牙进行牙髓摘除和根管充填,然后向近中移动6个月。
实验组细胞因子信使核糖核酸和蛋白质的表达在48小时后,在10kPa拉伸力加载时达到峰值(P <.01)。Gd(3+)降低了这些细胞因子信使核糖核酸的表达和蛋白质浓度(P <.01)。对照牙齿的炎性牙根吸收量明显大于牙髓摘除的牙齿(P <.05)。
本研究表明,牙髓细胞中的拉伸力通过S-A通道增强了各种细胞因子的表达,这可能导致牙齿移动过程中的炎性牙根吸收。这也表明根管治疗对牙齿移动过程中进行性严重炎性牙根吸收有效。