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Erosive-abrasive tissue loss in dentine under simulated bulimic conditions

机译:模拟的暴食条件下牙本质的磨蚀性磨蚀性组织损失

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Objectives: The eroded organic dentine matrix is remarkably resistant to mechanical impacts. Additional brushing abrasion of eroded dentine has only limited influence on tissue loss. Digestive enzymes (e.g., pepsin, trypsin) that can reach the oral cavity during reflux or vomiting can partially degrade the matrix. This degradation may have an influence on both the stability of the matrix against mechanical forces and the susceptibility of eroded dentine to combined chemo-mechanical impacts. Both were investigated in the present study. Methods: Dentine samples of four groups were cyclically demineralised (6 × 2 min/day, 9 days) with an HCl-pepsin-solution (pH 1.6, 1.5 mg/ml pepsin) and treated with a trypsin-solution (6 × 10 min/day, 2000 BAEE units/ml) directly afterwards. One group served as control; specimens of three groups were additionally brushed (2 × 15 s/day) directly after the first and last trypsin treatment with forces of 200 g, 300 g, and 400 g. Loss of demineralised and mineralised tissue was determined profilometrically. Additionally, an SEM analysis was performed. Results: Loss of mineralised tissue (μm, mean ± SD) was: 135.7 ± 10.9 (control), 165.2 ± 30.8 (200 g), 168.0 ± 16.3 (300 g), and 174.9 ± 17.1 (400 g). Tissue loss was increased significantly (p ≤ 0.001) by brushing independently of the force used (n.s. between brushed groups). SEM revealed that in all groups, the matrix was equally thinned through enzymatic activity, but it was still present as a continuous band. Conclusion: The results indicate that brushing of dentine after impact of acid and enzymes resulted in an increased tissue loss; however, the matrix persisted on the surface despite enzymatic treatment and brushing with forces of up to 400 g.
机译:目标:侵蚀的有机牙本质基质显着抵抗机械冲击。侵蚀的牙本质的额外刷磨磨损对组织损失的影响有限。在反流或呕吐过程中可以到达口腔的消化酶(例如胃蛋白酶,胰蛋白酶)可以部分降解基质。这种降解可能既影响基质抵抗机械力的稳定性,也影响侵蚀的牙本质对化学机械冲击的敏感性。两者都在本研究中进行了调查。方法:用盐酸胃蛋白酶溶液(pH 1.6,1.5 mg / ml胃蛋白酶)对四组牙本质样品进行循环脱盐(6×2分钟/天,9天)并用胰蛋白酶溶液处理(6×10分钟) /天,即2000 BAEE单位/毫升)。一组作为对照。在第一个和最后一个胰蛋白酶处理后,分别用200 g,300 g和400 g的力分别刷洗(3×2 x 15 s / day)的三组标本。脱矿质和矿化组织的损失通过轮廓测定法确定。另外,进行了SEM分析。结果:矿化组织的损失(μm,平均值±SD)为:135.7±10.9(对照),165.2±30.8(200克),168.0±16.3(300克)和174.9±17.1(400克)。通过刷涂而与所用力无关(刷涂组之间的鼻塞),组织损失显着增加(p≤0.001)。扫描电镜显示,在所有组中,基质均通过酶促活性变薄,但仍以连续带的形式存在。结论:结果表明,在酸和酶的作用下刷牙本质会增加组织的损失。然而,尽管经过酶处理和高达400 g的力刷涂,基质仍保留在表面上。

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