Finnish Doctoral Program in Oral Sciences (FINDOS), University of Turku, Institute of Dentistry, Turku, Finland; Department of Restorative Dentistry, and Cariology, and Adhesive Dentistry Research Group, Institute of Dentistry, University of Turku, Finland.
Department of Restorative Dentistry, and Cariology, and Adhesive Dentistry Research Group, Institute of Dentistry, University of Turku, Finland; Turku University Hospital, TYKS, University of Turku, Turku, Finland.
Dent Mater. 2017 Feb;33(2):e62-e68. doi: 10.1016/j.dental.2016.09.036. Epub 2016 Oct 10.
Inactivation of dentin proteases by crosslinkers has been suggested as a way to prevent the degradation of dentin collagen in the hybrid layer. However, it is not known if the inhibition is reversible. The aim of this study was to evaluate the inactivation effect of various crosslinkers on dentin protease activity over a period of 6 months.
Demineralized dentin beams (1×2×6mm, n=10/group) were treated with (1) 1% glutaraldehyde (GA1), (2) 5% glutaraldehyde (GA5), (3) 1% grape seed extract (GS1), (4) 5% grape seed extract (GS5), (5) 10% sumac berry extract (S), (6) 20μM curcumin (CR20), and (7) 200μM curcumin (CR200) for 5min. Untreated beams served as control. The beams were incubated up to 6 months and incubation media were used to analyze solubilized telopeptide (ICTP and CTX) fragments as indicators of MMP- and cathepsin K-mediated degradation after 1, 3 and 6 months of incubation. The relative MMP activity of dentin beams was tested using a generic MMP assay. Data were analyzed using repeated-measures ANOVA, α=0.05.
All treated groups showed significant decrease in CTX release (32.2-469.5pg/mg dentin) and ICTP (1.8-47.6ng/mg dentin) fragments during the first month of incubation compared to control (1159pg/mg and 72.9ng/mg dentin, respectively). GA5, GS5 and CR200 maintained their inhibitory effect during 6-month incubation. The results were confirmed by dry mass loss and relative MMP activity following 6 months.
The results of this study indicate that the long-term effect is both crosslinker and dose dependent.
交联剂使牙本质蛋白酶失活被认为是防止混合层中牙本质胶原降解的一种方法。然而,其抑制作用是否可逆尚不清楚。本研究旨在评估不同交联剂对牙本质蛋白酶活性的失活作用,时间跨度为 6 个月。
用(1)1%戊二醛(GA1)、(2)5%戊二醛(GA5)、(3)1%葡萄籽提取物(GS1)、(4)5%葡萄籽提取物(GS5)、(5)10%漆树莓提取物(S)、(6)20μM 姜黄素(CR20)和(7)200μM 姜黄素(CR200)处理脱矿牙本质梁(1×2×6mm,每组 10 个)5min。未处理的牙本质梁作为对照。将梁在孵育长达 6 个月,使用孵育介质分析可溶的末端肽(ICTP 和 CTX)片段,作为 MMP 和组织蛋白酶 K 介导的降解的指标,孵育 1、3 和 6 个月后。使用通用 MMP 测定法测试牙本质梁的相对 MMP 活性。使用重复测量方差分析,α=0.05 对数据进行分析。
与对照组(分别为 1159pg/mg 和 72.9ng/mg 牙本质)相比,所有处理组在孵育的第一个月中 ICTP(1.8-47.6ng/mg 牙本质)和 CTX(32.2-469.5pg/mg 牙本质)片段的释放均显著减少。GA5、GS5 和 CR200 在 6 个月的孵育期间保持抑制作用。6 个月后的干重损失和相对 MMP 活性证实了这一结果。
本研究结果表明,长期效果既依赖于交联剂又依赖于剂量。