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Effects of pulpectomy on the amount of root resorption during orthodontic tooth movement

机译:拔髓对正畸牙齿移动过程中牙根吸收量的影响

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Introduction 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. Methods 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 (Gd3+) 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. Results 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). Gd3+ 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). Conclusions 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.
机译:前言先前的研究表明,正畸力会通过血管破裂和牙髓组织空泡影响牙髓。我们假设过大的正畸力后,牙髓组织会表达炎症细胞因子和牙本质细胞分化的调节因子。这项研究的目的是研究张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炎症性根吸收。方法在人牙髓细胞上施加循环张力后,通过实时聚合酶法测定巨噬细胞集落刺激因子,核因子κB配体的受体激活剂,白介素-1β和肿瘤坏死因子α的基因表达和蛋白浓度。链反应和酶联免疫测定。此外,通过g(Gd3 +)处理评估了拉伸激活通道的作用。对7周Wistar大鼠的右上第一磨牙进行牙髓切除和根管充填,然后进行近中生运动6个月。结果实验组细胞因子信使RNA和蛋白质的表达在48小时后以10kPa的拉力负荷达到峰值(P <0.01)。 Gd3 +降低了这些细胞因子信使RNA的表达和蛋白质浓度(P <.01)。对照牙的炎症性根吸收量显着大于经牙髓切除的牙(P <.05)。结论这项研究表明,牙髓细胞中的张力通过S-A通道增强了各种细胞因子的表达,这可能导致牙齿运动过程中炎症性牙根吸收。这也表明,根管治疗对于牙齿运动过程中进行性严重炎症性根吸收有效。

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