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来自巴西腰果树上的漆树酸可减少牙本质侵蚀。

Anacardic acid from brazilian cashew nut trees reduces dentine erosion.

作者信息

Silveira Cintia, Oliveira Flávia, Dos Santos Maria Lucilia, de Freitas Thiago, Imparato José Carlos, Magalhães Ana Carolina

机构信息

Department of Pediatric Dentistry, School of Dentistry, São Leopoldo Mandic Dental Research Center, Campinas, Brazil.

出版信息

Caries Res. 2014;48(6):549-56. doi: 10.1159/000358400. Epub 2014 Jul 3.

Abstract

The aim of this study was to analyze the effect of solutions containing saturated anacardic acid (AA) on dentine erosion in vitro. AA was chemically isolated from natural cashew nutshell liquid obtained by continuous extraction in a Soxhlet extractor and was fully saturated by catalytic hydrogenation. Matrix metalloproteinase 2 (MMP-2) activity, when exposed to buffers containing 100 µmol/l AA, was analyzed using zymography. Bovine root samples were subjected to erosive demineralization (Sprite Zero™, 4 × 90 s/day) and remineralization with artificial saliva between the erosive cycles for 5 days. The samples were treated as follows, after the first and the last acid exposure (1 min; n = 12/group): (1) 100 µmol/l epigallocatechin-3-gallate (EGCG) (positive control); (2) 0.05% NaF; (3) 100 µmol/l saturated AA; (4) saturated AA and EGCG; (5) saturated AA, EGCG and NaF; (6) untreated (negative control). Dentine erosion was measured using a contact profilometer. Two dentine samples from each group were analyzed using scanning electron microscopy. Saturated AA reduced the activity of MMP-2. ANOVA and Tukey's test revealed that all treatments significantly reduced dentine loss compared to the negative control (6.03 ± 0.98 µm). Solutions containing saturated AA (1.97 ± 1.02 µm) showed the greatest reduction in dentine erosion compared to the NaF (3.93 ± 1.54 µm) and EGCG (3.79 ± 0.83 µm) solutions. Therefore, it may be concluded that AA significantly reduces dentine erosion in vitro, possibly by acting as an MMP-2 inhibitor.

摘要

本研究的目的是分析含有饱和漆树酸(AA)的溶液对体外牙本质侵蚀的影响。AA是从通过索氏提取器连续萃取获得的天然腰果壳液中化学分离出来的,并通过催化氢化使其完全饱和。使用酶谱法分析了基质金属蛋白酶2(MMP - 2)在暴露于含有100μmol/L AA的缓冲液时的活性。牛牙根样本进行侵蚀性脱矿(零度雪碧™,每天4×90秒),并在侵蚀周期之间用人造唾液再矿化5天。在第一次和最后一次酸暴露(1分钟;每组n = 12)后,对样本进行如下处理:(1)100μmol/L表没食子儿茶素 - 3 - 没食子酸酯(EGCG)(阳性对照);(2)0.05%氟化钠;(3)100μmol/L饱和AA;(4)饱和AA和EGCG;(5)饱和AA、EGCG和氟化钠;(6)未处理(阴性对照)。使用接触式轮廓仪测量牙本质侵蚀。每组取两个牙本质样本用扫描电子显微镜进行分析。饱和AA降低了MMP - 2的活性。方差分析和Tukey检验显示,与阴性对照(6.03±0.98μm)相比,所有处理均显著减少了牙本质损失。与氟化钠(3.93±1.54μm)和EGCG(3.79±0.83μm)溶液相比,含有饱和AA的溶液(1.97±1.02μm)在牙本质侵蚀减少方面表现最为显著。因此,可以得出结论,AA可能通过作为MMP - 2抑制剂在体外显著减少牙本质侵蚀。

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