Department of Dental General and Emergency, The Affiliated Stomatological Hospital of Nanchang University, No. 688 Honggu North Road, Honggutan District, Nanchang, 330038, People's Republic of China.
The Key Laboratory of Oral Biomedicine, Nanchang, Jiangxi Province, People's Republic of China.
Sci Rep. 2023 Jun 9;13(1):9413. doi: 10.1038/s41598-023-35382-3.
This study aimed to evaluate the effect of theaflavins [TFs] on the process of dentin erosion and investigation the potential mechanism. For erosion kinetics of the dentin, 7 experimental groups (n = 5) treated with 10% ethanol [EtOH] (negative control) are erosion for 1, 2, 3, 4, 5, 6, and 7 d erosion cycles (4 cycles/d). For the effect of TFs on dentin erosion, 6 experimental groups (n = 5) were treated with 1% epigallocatechin gallate [EGCG], 1% chlorhexidine [CHX], 1%, 2%, 4%, and 8% TFs for the 30 s and then subjected to erosion cycles (4 cycles/d for 7 d). The erosive dentin wear (μm) and surface morphology were evaluated and compared by laser scanning confocal microscope and scanning electron microscopy. The matrix metalloproteinase inhibition effects of TFs were investigated using in situ zymography and molecular docking. TFs-treated collagen was investigated by ultimate microtensile strength, Fourier-transform infrared spectroscopy, and molecular docking. Data were analyzed by ANOVA, Tukey's test (P < 0.05). The TFs-treated groups (7.56 ± 0.39, 5.29 ± 0.61, 3.28 ± 0.33, and 2.62 ± 0.99 μm for 1%, 2%, 4%, and 8% TFs) had significantly lower erosive dentin wear than the negative control group (11.23 ± 0.82 μm), and the effect was concentration-dependent at low concentrations (P < 0.05). TFs inhibit matrix metalloproteinase [MMP]. Moreover, TFs crosslink dentin collagen and cause hydrophilic changes in dentin collagen. TFs preserve organic matrix within the demineralized dentin by inhibiting MMP activity and simultaneously improving collagen's resistance to enzymes, both of which contribute to preventing or slowing down the progression of dentin erosion.
本研究旨在评估茶黄素(TFs)对牙本质侵蚀过程的影响,并探讨其潜在机制。对于牙本质的侵蚀动力学,将 7 个实验组(n=5)用 10%乙醇(EtOH)(阴性对照)处理 1、2、3、4、5、6 和 7 d 侵蚀循环(4 个循环/d)。对于 TFs 对牙本质侵蚀的影响,将 6 个实验组(n=5)用 1%表没食子儿茶素没食子酸酯(EGCG)、1%洗必泰(CHX)、1%、2%、4%和 8% TFs 处理 30 s,然后进行侵蚀循环(7 d 内 4 个循环/d)。用激光扫描共聚焦显微镜和扫描电子显微镜评估和比较侵蚀性牙本质磨损(μm)和表面形态。通过原位酶谱和分子对接研究 TFs 的基质金属蛋白酶抑制作用。用最终微拉伸强度、傅里叶变换红外光谱和分子对接研究 TFs 处理的胶原蛋白。用方差分析、Tukey 检验(P<0.05)分析数据。与阴性对照组(11.23±0.82 μm)相比,TFs 处理组(1%、2%、4%和 8% TFs 的牙本质磨损分别为 7.56±0.39、5.29±0.61、3.28±0.33 和 2.62±0.99 μm)的牙本质磨损明显较低,且在低浓度时呈浓度依赖性(P<0.05)。TFs 抑制基质金属蛋白酶[MMP]。此外,TFs 交联牙本质胶原蛋白并导致牙本质胶原蛋白发生亲水性变化。TFs 通过抑制 MMP 活性同时提高胶原蛋白对酶的抵抗力来保护脱矿牙本质内的有机基质,这两者都有助于防止或减缓牙本质侵蚀的进展。