体外交联处理后牙本质基质的稳定性
Stabilization of dentin matrix after cross-linking treatments, in vitro.
作者信息
Scheffel Débora L S, Hebling Josimeri, Scheffel Régis H, Agee Kelli A, Cadenaro Milena, Turco Gianluca, Breschi Lorenzo, Mazzoni Annalisa, Costa Carlos A de Souza, Pashley David H
机构信息
Department of Orthodontics and Pediatric Dentistry, Araraquara School of Dentistry, UNESP - Univ Estadual Paulista, Araraquara, São Paulo, Brazil.
Department of Oral Biology, College of Dental Medicine, Georgia Regents University, Augusta, GA, USA.
出版信息
Dent Mater. 2014 Feb;30(2):227-33. doi: 10.1016/j.dental.2013.11.007. Epub 2013 Dec 13.
OBJECTIVES
To evaluate the effect of EDC on elastic modulus (E), MMPs activity, hydroxyproline (HYP) release and thermal denaturation temperature of demineralized dentin collagen.
METHODS
Dentin beams were obtained from human molars and completely demineralized in 10 wt% H3PO4 for 18 h. The initial E and MMP activity were determined with three-point bending and microcolorimetric assay, respectively. Extra demineralized beams were dehydrated and the initial dry mass (DM) was determined. All the beams were distributed into groups (n=10) and treated for 30 s or 60 s with: water, 0.5 M, 1 M or 2 M EDC or 10% glutaraldehyde (GA). After treatment, the new E and MMP activity were redetermined. The beams submitted to DM measurements were storage for 1 week in artificial saliva, after that the mass loss and HYP release were evaluated. The collagen thermal denaturation temperature (TDT) was determined by DSC analysis. Data for E, MMP activity and HYP release were submitted to Wilcoxon and Kruskal-Wallis or Mann-Whitney tests. Mass loss and TDT data were submitted to ANOVA and Tukey tests at the 5% of significance.
RESULTS
EDC was able to significantly increase collagen stiffness in 60s. 10% GA groups obtained the highest E values after both 30 and 60s. All cross-linking agents decreased MMP activity and HYP release and increased TDT temperature. Significant differences were identified among EDC groups after 30 or 60 s of cross-linking, 1M or 2M EDC showed the lowest MMP activity.
SIGNIFICANCE
Cross-linking agents are capable of preventing dentin collagen degradation. EDC treatment may be clinically useful to increase resin-dentin stability.
目的
评估乙二醛(EDC)对脱矿牙本质胶原蛋白弹性模量(E)、基质金属蛋白酶(MMPs)活性、羟脯氨酸(HYP)释放及热变性温度的影响。
方法
从人磨牙获取牙本质梁,在10 wt%磷酸中完全脱矿18小时。分别采用三点弯曲和微量比色法测定初始弹性模量和MMP活性。将额外的脱矿梁脱水并测定初始干质量(DM)。所有梁分为若干组(n = 10),分别用水、0.5 M、1 M或2 M EDC或10%戊二醛(GA)处理30秒或60秒。处理后,重新测定新的弹性模量和MMP活性。进行DM测量的梁在人工唾液中储存1周,之后评估质量损失和HYP释放。通过差示扫描量热法(DSC)分析测定胶原蛋白热变性温度(TDT)。将弹性模量、MMP活性和HYP释放的数据进行Wilcoxon检验、Kruskal-Wallis检验或Mann-Whitney检验。质量损失和TDT数据进行方差分析(ANOVA)和Tukey检验,显著性水平为5%。
结果
EDC能够在60秒时显著增加胶原蛋白硬度。10% GA组在30秒和60秒后均获得最高的弹性模量值。所有交联剂均降低MMP活性和HYP释放,并提高TDT温度。交联30秒或60秒后,EDC各组之间存在显著差异,1 M或2 M EDC显示出最低的MMP活性。
意义
交联剂能够防止牙本质胶原蛋白降解。EDC处理在临床上可能有助于提高树脂与牙本质的稳定性。