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牙本质龋进展与金属蛋白酶的作用:最新进展

Dentin caries progression and the role of metalloproteinases: an update.

作者信息

Femiano F, Femiano R, Femiano L, Jamilian A, Rullo R, Perillo L

机构信息

Multidisciplinary Department of Medical-Surgical and Dental Specialties, Second University of Naples, Naples, Italy.

Department of Orthodontics, Cranio-Maxillofacial Research Center, Islamic Azad University, Tehran, Iran.

出版信息

Eur J Paediatr Dent. 2016 Sep;17(3):243-247.

Abstract

AIM

This review aims to summarise our understanding of the destructive role of acid environment and metalloproteinases in dentin caries progression using a review process.

METHOD

The acids resulting from consumption of sugars by acidogenic and aciduric bacteria can cause demineralisation of the tooth surface, but are not able to cause caries-like lesions. The appearance of such lesions requires the activation of enzymatic proteolysis in an acidic environment for degradation of the dentin organic matrix, leading to cavity formation. Bacterial collagenases have long been considered responsible for organic matrix destruction; host cell-derived matrix metalloproteinases (MMPs) have recently been considered to be involved in the dentinal matrix destruction of carious lesions.

DISCUSSION AND CONCLUSION

MMPs are initially synthesised as inactive zymogens to be activated in acid environment of dentinal fluid during the carious process, resulting in destruction of the collagenous matrix. The role of acid environment on enamel and dentin demineralisation and the role of salivary and dentinal MMPs in dentin progression of caries has encouraged general dentists to include the monitoring of oral environment not only by control of bacterial oral flora in caries treatment protocol, but mainly by inhibition of dentinal and salivary MMPs through the use of toothpaste and/or mouthwash containing specific active agents.

摘要

目的

本综述旨在通过综述过程总结我们对酸性环境和金属蛋白酶在牙本质龋进展中的破坏作用的理解。

方法

产酸和耐酸细菌消耗糖类产生的酸可导致牙齿表面脱矿,但不能引起龋样病变。此类病变的出现需要在酸性环境中激活酶促蛋白水解以降解牙本质有机基质,从而导致龋洞形成。长期以来,细菌胶原酶一直被认为是导致有机基质破坏的原因;宿主细胞衍生的基质金属蛋白酶(MMPs)最近被认为参与了龋损的牙本质基质破坏。

讨论与结论

MMPs最初以无活性的酶原形式合成,在龋病过程中在牙本质液的酸性环境中被激活,导致胶原基质的破坏。酸性环境对釉质和牙本质脱矿的作用以及唾液和牙本质MMPs在牙本质龋进展中的作用,促使普通牙医在龋病治疗方案中不仅要通过控制口腔细菌菌群来监测口腔环境,而且主要是通过使用含有特定活性剂的牙膏和/或漱口水来抑制牙本质和唾液中的MMPs。

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