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山奈酚通过抑制基质金属蛋白酶和促进牙本质生物改性中的胶原蛋白交联对牙本质粘结稳定性的影响。

The effect of kaempferol on the dentin bonding stability through matrix metalloproteinases inhibition and collagen crosslink in dentin biomodification.

作者信息

Cho Jeonghwa, Kim Hyeryeong, Yoo Kyung-Hyeon, Paik Youna, Kim In-Ryoung, Yoon Seog-Young, Kim Yong-Il

机构信息

Department of Orthodontics, Dental Research Institute, Pusan National University Dental Hospital, Yangsan, South Korea.

School of Materials Science and Engineering, Pusan National University, Busan, South Korea.

出版信息

J Dent Sci. 2023 Jul;18(3):1023-1030. doi: 10.1016/j.jds.2022.12.002. Epub 2022 Dec 14.

Abstract

BACKGROUND/PURPOSE: Naturally derived collagen crosslinkers with matrix metalloproteinases (MMPs) inhibitory activity for dentin bonding have been previously studied. One of these crosslinkers is flavonoids. The purpose of this study was to investigate whether dentin pretreatment with kaempferol (KEM), one of the flavonoids, enhances dentin bond stability and nanoleakage at the dentin-resin interface through MMPs inhibition and collagen crosslinking.

MATERIALS AND METHODS

The experimental KEM-containing solution was used to pretreat demineralized dentin prior to the application of a universal adhesive. KEM is a natural flavonoid and those which did not take the experimental solution served as the control group (CON). Microtensile bond strength (μTBS) and nanoleakage tests were conducted before and after the thermocycling to evaluate the influence of KEM on dentin bond strength. The MMPs inhibition activity of KEM was analyzed via MMPs zymography using a confocal microscopy. Fourier-transform infrared (FTIR) spectroscopy was used to demonstrate that KEM inhibits MMPs and enhances collagen crosslinking.

RESULTS

The μTBS values of KEM group exhibited a higher bond strength after thermocycling. At the resin-dentin interface, the KEM group did not exhibit any signs of nanoleakage after thermocycling. Furthermore, MMPs zymography confirmed that there was a relatively low activity of MMPs in the presence of KEM. In FTIR analysis, the PO peak representing the cross-link between dentin and collagen was significantly higher in the KEM group.

CONCLUSION

Our findings suggest that pretreatment with KEM enhances the dentin bonding stability at the resin-dentin interface by acting as a collagen crosslinker and MMPs inhibitor.

摘要

背景/目的:先前已对具有基质金属蛋白酶(MMPs)抑制活性的天然衍生胶原蛋白交联剂用于牙本质粘结进行了研究。这些交联剂之一是黄酮类化合物。本研究的目的是调查用黄酮类化合物之一的山奈酚(KEM)预处理牙本质是否通过抑制MMPs和交联胶原蛋白来增强牙本质-树脂界面处的粘结稳定性和纳米渗漏。

材料与方法

在应用通用粘结剂之前,使用含KEM的实验溶液预处理脱矿牙本质。KEM是一种天然黄酮类化合物,未使用实验溶液的作为对照组(CON)。在热循环前后进行微拉伸粘结强度(μTBS)和纳米渗漏测试,以评估KEM对牙本质粘结强度的影响。通过共聚焦显微镜使用MMPs酶谱分析法分析KEM的MMPs抑制活性。傅里叶变换红外(FTIR)光谱用于证明KEM抑制MMPs并增强胶原蛋白交联。

结果

热循环后,KEM组的μTBS值显示出更高的粘结强度。在树脂-牙本质界面处,热循环后KEM组未表现出任何纳米渗漏迹象。此外,MMPs酶谱分析证实,在有KEM存在的情况下,MMPs的活性相对较低。在FTIR分析中,代表牙本质与胶原蛋白之间交联的PO峰在KEM组中明显更高。

结论

我们的研究结果表明,用KEM预处理可通过作为胶原蛋白交联剂和MMPs抑制剂来增强树脂-牙本质界面处的牙本质粘结稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974a/10316434/8e1f2ad0b2f0/gr1.jpg

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