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橙皮苷对牙本质胶原降解的抑制作用:一项原位研究。

Inhibition of dentine collagen degradation by hesperidin: an in situ study.

作者信息

van Strijp Augustinus J P, Takatsuka Tsutomu, Sono Ryohei, Iijima Youichi

机构信息

Department of Cariology Endodontology Pedodontology, Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam and VU University Amsterdam, Amsterdam, the Netherlands.

Sunstar, Osaka, Japan.

出版信息

Eur J Oral Sci. 2015 Dec;123(6):447-52. doi: 10.1111/eos.12225. Epub 2015 Oct 29.

Abstract

Dentine caries is a process of demineralization and subsequent degradation of the collagenous matrix. Host-derived proteolytic enzymes, such as matrix metalloproteinases (MMPs), play a role in this process of dentine collagen degradation. Hampering this degradation retards the caries process. Dietary antioxidants, such as the flavonoid hesperidin, can inhibit the proteolytic activity of MMPs and act as natural stabilizers of collagen. The aim of this study was to investigate the anti-collagenolytic activity of hesperidin in an in situ model. A single-blind, split-mouth, in situ experiment was designed. Seventeen participants received two completely demineralized dentine specimens placed contralaterally in the buccal flanges of their partial prosthesis. During the 4-wk experimental period, the participants immersed the dentine specimens in a test solution [1,000 parts per million (p.p.m.) hesperidin] or a control solution (saline), twice daily for 3 min. After the in situ period, the specimens were retrieved and their collagen content was determined. A saliva sample was taken at the start and at the end of the experimental period, to assess collagenolytic activity. A significant protection of collagen, of 24%, was observed in the hesperidin-treated specimens compared with the control-treated specimens. No correlation was found between salivary collagenolytic activity and loss of collagen in the control-treated specimens. The results of this in situ study show that hesperidin could play a role in the preservation of dentine collagen matrix.

摘要

牙本质龋是一个牙本质胶原基质脱矿及随后降解的过程。宿主来源的蛋白水解酶,如基质金属蛋白酶(MMPs),在牙本质胶原降解过程中发挥作用。抑制这种降解可延缓龋病进程。膳食抗氧化剂,如类黄酮橙皮苷,可抑制MMPs的蛋白水解活性,并作为胶原的天然稳定剂。本研究的目的是在原位模型中研究橙皮苷的抗胶原溶解活性。设计了一项单盲、双侧对照的原位实验。17名参与者在其局部义齿的颊侧基托中对侧放置两个完全脱矿的牙本质标本。在为期4周的实验期内,参与者将牙本质标本每天两次浸泡在测试溶液[百万分之一(ppm)的橙皮苷]或对照溶液(生理盐水)中,每次浸泡3分钟。原位实验期结束后,取出标本并测定其胶原含量。在实验期开始和结束时采集唾液样本,以评估胶原溶解活性。与对照处理的标本相比,橙皮苷处理的标本中胶原得到了24%的显著保护。在对照处理的标本中,未发现唾液胶原溶解活性与胶原损失之间存在相关性。这项原位研究的结果表明,橙皮苷可能在保护牙本质胶原基质方面发挥作用。

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