Lee Won Sek, Kim Yeon, Bae Moon-Kyoung, Yoo Kyung-Hyeon, Park Hae Ryoun, Kim Yong-I I
Department of Orthodontics, Dental Research Institute, Pusan National University, Yangsan, 50612, South Korea.
Department of Oral Physiology, School of Dentistry, Pusan National University, Yangsan, 50612, South Korea.
Int J Nanomedicine. 2024 Dec 9;19:13253-13265. doi: 10.2147/IJN.S490667. eCollection 2024.
To evaluate the effects of fucosterol and fucoxanthin on ultimate microtensile strength (µUTS), dentin collagen cross-linking, erosion resistance, and matrix metalloproteinase (MMP) inhibition.
Dentin beams and slices were prepared from extracted human teeth and treated with concentrations of 50 µg/mL, 100 µg/mL, and 200 µg/mL of fucosterol and fucoxanthin. Fourier-transform infrared spectroscopy (FTIR) was used to analyze collagen cross-linking. In situ zymography was used to quantify MMP activity inhibition. Molecular docking simulations were used to gain insights into the binding interactions between the compounds and dentin collagen/MMPs. In vitro erosion tests and 3D non-contact profilometry were used to evaluate erosion resistance. µUTS was measured to assess mechanical enhancement.
FTIR analysis showed increased collagen cross-linking in fucosterol and fucoxanthin treated groups, with notable shifts in amide II bands in a concentration-dependent manner. In situ zymography revealed effective MMP inhibition in fucosterol and fucoxanthin treated samples, with inhibition increasing at higher concentrations, supporting the stabilization of the dentin matrix. Molecular docking confirmed favorable binding interactions between the compounds and both collagen and MMPs. Erosion tests demonstrated significantly reduced dentin structure loss and surface roughness in the experimental samples. Treatment with fucosterol and fucoxanthin significantly increased µUTS values, compared to controls, indicating enhanced dentin strength.
Fucosterol and fucoxanthin from marine algae effectively enhance dentin mechanical properties and resistance to acid-induced erosion through collagen cross-linking and MMP inhibition. These findings suggest that these compounds could serve as promising natural treatments for dentin preservation against acid attacks, potentially improving oral health outcomes.
评估岩藻甾醇和岩藻黄质对极限微拉伸强度(µUTS)、牙本质胶原交联、抗侵蚀性及基质金属蛋白酶(MMP)抑制作用的影响。
从拔除的人牙制备牙本质梁和切片,并用浓度为50 µg/mL、100 µg/mL和200 µg/mL的岩藻甾醇和岩藻黄质进行处理。采用傅里叶变换红外光谱(FTIR)分析胶原交联。采用原位酶谱法量化MMP活性抑制。利用分子对接模拟深入了解化合物与牙本质胶原/MMPs之间的结合相互作用。采用体外侵蚀试验和三维非接触轮廓仪评估抗侵蚀性。测量µUTS以评估力学增强效果。
FTIR分析显示,岩藻甾醇和岩藻黄质处理组的胶原交联增加,酰胺II带呈浓度依赖性显著位移。原位酶谱显示,岩藻甾醇和岩藻黄质处理的样品中MMP受到有效抑制,且在较高浓度下抑制作用增强,支持了牙本质基质的稳定性。分子对接证实了化合物与胶原和MMPs之间存在良好的结合相互作用。侵蚀试验表明,实验样品中牙本质结构损失和表面粗糙度显著降低。与对照组相比,岩藻甾醇和岩藻黄质处理显著提高了µUTS值,表明牙本质强度增强。
来自海藻的岩藻甾醇和岩藻黄质通过胶原交联和MMP抑制作用有效增强牙本质力学性能和抗酸蚀性。这些发现表明,这些化合物有望作为天然治疗方法用于保护牙本质免受酸侵蚀,潜在改善口腔健康状况。