In-situ zymography to assess the MMPs activity with different etching time and ethanol wet-bonding on radicular dentin

A. Comba, A. Baldi, M. Alovisi, D. Pasqualini, E. Berutti, L. Breschi, A. Mazzoni, N. Scotti
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Abstract

The aim of this in vitro study was to investigate the effect of different etching times and ethanol pre-treatment on metalloproteinasis (MMPs) gelatinolytic activity on root dentin. Twelve single root teeth, extracted for periodontal reasons, were selected and an endodontic treatment was performed. After seven days, an 8-mm post space was prepared with dedicated drills. Specimens were randomly divided into four groups according to different adhesive protocols, based on different etching time in phosphoric acid and pre-treatment application. Cementation of the fiber post was performed with a dual-curing cement (DC Core, Kuraray) polymerized for 40s. In situ zymographic analyses was performed to investigate endogenous MMPs activity within the dentin hybrid layer. Quantification analyses of the MMPs activity revealed that all tested groups activated enzymes. However, the ethanol wet-bonding pretreatment was able to reduce the MMPs activity, above all when radicular dentin was extensively etched. In conclusion, MMPs gelatinolytic activity was detected in all groups and in-situ zymography was able to measure it. Further investigations are needed to clinically validate the data obtained of the present study.
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原位酶谱法评价不同蚀刻时间和乙醇在牙根状牙本质上湿键合的MMPs活性
本实验旨在探讨不同蚀刻时间和乙醇预处理对金属蛋白酶(MMPs)根本质溶胶活性的影响。选择12颗因牙周原因拔出的单根牙,进行根管治疗。7天后,用专用钻头准备一个8毫米的柱空间。根据不同的粘接方案,根据不同的磷酸蚀刻时间和预处理应用,将标本随机分为四组。采用双固化水泥(DC Core, Kuraray)聚合40秒,对纤维桩进行胶结。原位酶谱分析研究了牙本质杂交层内源性MMPs的活性。定量分析MMPs活性显示,所有测试组都激活了酶。然而,乙醇湿键预处理能够降低MMPs活性,尤其是当根状牙本质被广泛蚀刻时。综上所述,在所有组中均检测到MMPs的明胶溶解活性,并且原位酶谱法能够测量其活性。需要进一步的研究来临床验证本研究获得的数据。
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