Lv Xueping, Yang Yang, Han Sili, Li Danxue, Tu Huanxin, Li Wei, Zhou Xuedong, Zhang Linglin
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, 610041, PR China.
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, 610041, PR China.
Arch Oral Biol. 2015 Oct;60(10):1482-7. doi: 10.1016/j.archoralbio.2015.07.010. Epub 2015 Jul 19.
In this study we give a preliminary study of a rationally designed small peptide, which is based on the enamel matrix protein amelogenin, to investigate its effect on remineralization of initial enamel caries lesions.
A novel peptide was designed and synthesized to investigate its effects on the remineralization of initial enamel carious lesions during pH cycling that simulates intra-oral conditions. Initial lesions were created in bovine enamel blocks, which were then pH-cycled for 12 days in the presence of 25μM peptide, 1g/L NaF (positive control), 50mM HEPES buffer(negative control). Before and after pH cycling, enamel blocks were analyzed by surface microhardness testing, polarized light microscopy and transverse microradiography.
Percentage of surface microhardness recovery (SMHR%) after pH cycling was significantly higher in peptide group than HEPES group. Lower lesion depth and less mineral mineral loss were found in peptide or NaF treatment groups after the cycling, and were significantly different to HEPES group. No significant differences were observed between the blocks treated with peptide and those treated with NaF.
This study provides in vitro evidence that this amelogenin based peptide promotes enamel caries remineralization, offering a promising remineralizing biomaterial in initial enamel carious treatment.
在本研究中,我们对一种基于牙釉质基质蛋白釉原蛋白合理设计的小肽进行了初步研究,以探讨其对早期牙釉质龋损再矿化的影响。
设计并合成了一种新型肽,以研究其在模拟口腔环境的pH循环过程中对早期牙釉质龋损再矿化的影响。在牛牙釉质块中制备初始龋损,然后在存在25μM肽、1g/L氟化钠(阳性对照)、50mM HEPES缓冲液(阴性对照)的情况下进行12天的pH循环。在pH循环前后,通过表面显微硬度测试、偏光显微镜和横向显微放射摄影对牙釉质块进行分析。
肽组在pH循环后的表面显微硬度恢复百分比(SMHR%)显著高于HEPES组。循环后,肽或氟化钠处理组的病变深度较低,矿物质损失较少,与HEPES组有显著差异。用肽处理的块与用氟化钠处理的块之间未观察到显著差异。
本研究提供了体外证据,表明这种基于釉原蛋白的肽促进牙釉质龋再矿化,为早期牙釉质龋治疗提供了一种有前景的再矿化生物材料。