Department of Biomedical and Neuromotor Sciences, DIBINEM, University of Bologna-Alma Mater Studiorum, Via San Vitale 59, 40125 Bologna, Italy.
Area of Stomatology, Health Sciences Faculty, King Juan Carlos University, Avda. de Atenas, 28922 Alcorcón, Spain.
Int J Mol Sci. 2021 Aug 17;22(16):8852. doi: 10.3390/ijms22168852.
The aim of this study was to evaluate the effect of different concentrations of chitosan polymer on dentinal enzymatic activity by means of gelatin and in situ zymography. Human dentin was frozen and ground in a miller. Dentin powder aliquots were demineralized with phosphoric acid and treated with three different concentrations of lyophilized chitosan polymer (1, 0.5 and 0.1 wt%) dissolved in distilled water. Dentin proteins were extracted from each experimental group and electrophoresed under non-reducing conditions in 10% SDS-PAGE containing fluorescein-labeled gelatin. After 48 h in the incubation buffer at 37 °C, proteolytic activity was registered under long-wave UV light scanner and quantified by using Image J software. Furthermore, additional teeth ( = 4) were prepared for the in situ zymographic analysis in unrestored as well as restored dentin pretreated with the same chitosan primers. The registered enzymatic activity was directly proportional to the chitosan concentration and higher in the restored dentin groups ( < 0.05), except for the 0.1% chitosan primer. Chitosan 0.1% only showed faint expression of enzymatic activity compared to 1% and 0.5% concentrations. Chitosan 0.1% dissolved in water can produce significant reduction in MMPs activity and could possibly contribute to bond strength preservation over time.
本研究旨在通过明胶和原位酶谱法评估不同浓度壳聚糖聚合物对牙本质酶活性的影响。将人牙本质冷冻并在研磨机中研磨。将牙本质粉末等分试样用磷酸脱矿并用三种不同浓度的冻干壳聚糖聚合物(1、0.5 和 0.1wt%)溶解在蒸馏水中处理。从每个实验组中提取牙本质蛋白,并在含有荧光标记明胶的 10%SDS-PAGE 中进行非还原条件下的电泳。在 37°C 的孵育缓冲液中孵育 48 小时后,在长波紫外光扫描仪下记录蛋白水解活性,并使用 Image J 软件进行定量。此外,还对(=4)颗额外的牙齿进行了原位酶谱分析,这些牙齿未经修复以及用相同壳聚糖引发剂预处理的修复牙本质。登记的酶活性与壳聚糖浓度成正比,且在修复牙本质组中更高(<0.05),壳聚糖 0.1%引发剂除外。与 1%和 0.5%浓度相比,壳聚糖 0.1%仅显示出微弱的酶活性表达。溶于水的壳聚糖 0.1%可显著降低 MMPs 活性,并可能有助于随着时间的推移保持粘结强度。