期刊文献+

脱矿牙本质基质保护策略及其在牙本质-树脂粘接修复中的研究进展 被引量:4

Strategies for demineralized dentin matrix protection and its research progress in dentin-resin bonding restoration
原文传递
导出
摘要 病理损伤和临床医源性操作均可导致牙本质脱矿,形成脱矿牙本质基质(demineralized dentin matrix,DDM)。牙本质脱矿激活内源性基质金属蛋白酶(matrix metalloproteinase,MMP)和半胱氨酸组织蛋白酶(cysteine cathepsin,CC);同时DDM力学性能降低,因此在酶促降解和物理破坏下DDM易丧失结构完整性,降低DDM在牙本质-树脂粘接修复中的临床价值。采用交联剂和MMP/CC抑制剂是保护DDM结构完整性和实现其临床价值的有效策略。多种化学合成试剂和植物来源提取物能显著改善DDM力学性能,增强DDM酶解耐受性,但化学合成试剂的细胞毒性和植物提取物引起的牙齿着色可显著影响其临床适用性。在保护牙本质胶原的同时发挥抗菌性能是未来DDM保护剂研究的新方向。因此,本综述分别从胶原交联剂、胶原降解酶抑制剂和集两者功效于一体的化合物展开,探讨DDM保护的最新研究进展,并展望其在牙本质-树脂粘接中的应用前景,以期为DDM保护策略的临床应用提供参考。 Both pathological injuries and clinical iatrogenic operations can lead to dentin demineralization,forming demineralized dentin matrix(DDM).Dentin demineralization activates endogenous matrix metalloproteinase(MMP)and cysteine cathepsin(CC),and the mechanical properties of DDM decrease,so DDM is prone to lose its structural integrity under the action of enzymatic degradation and mechanical destruction,which in turn results in the reduction of clinical functional value of DDM in dentin-resin bonding restoration.The administrations of dentin collagen cross-linking reagents and MMP/CC inhibitors are effective strategies to protect DDM structural integrity and achieve its clinical functional value.A variety of chemically synthesized reagents and plant-derived extracts are capable of significantly improving the mechanical properties of DDM and enhancing its enzymatic tolerance.However,the cytotoxicity caused by chemically synthesized reagents and the tooth staining aroused by plant extracts have considerably affected their clinical applicability.Protecting dentin collagen while exerting antibacterial properties is a new direction for future DDM protective agent research.Accordingly,from the perspectives of cross-linking reagents,enzyme inhibitors and compounds which possess the dual proper ties,this review discusses the latest research progress in DDM protection,and looks into its application prospects in dentin-resin bonding,in an attempt to provide reference for the clinical promotion of DDM protection strategy.
作者 蔡明轩 毛靖 汪一帆 邹杰林 石鑫 Cai Mingxuan;Mao Jing;Wang Yifan;Zou Jielin;Shi Xin(Department of Orthodontics,Center of Stomatology,Tongji Hospital,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China)
出处 《中华口腔医学杂志》 CAS CSCD 北大核心 2021年第11期1144-1149,共6页 Chinese Journal of Stomatology
基金 湖北省卫生健康委员会重点项目(WJ2019Z006) 口腔颌面发育与再生湖北省重点实验室开放基金(2020kqhm002)。
关键词 牙本质 基质金属蛋白酶类 胶原酶类 酶抑制剂 交联试剂 脱矿牙本质基质 半胱氨酸组织蛋白酶 Dentin Matrix metalloproteinases Collagenases Enzyme inhibitors Cross-linking reagents Demineralized dentin matrix Cysteine cathepsin
  • 相关文献

参考文献3

二级参考文献21

  • 1Breschi L, Mazzoni A, Ruggeri A, et al. Dental adhesion review: aging and stability of the bonded interface. Dent Mater, 2008, 24(1) : 90-101.
  • 2Tam L, Jokstad A. The bond between resin composite restorations and dentin may degrade in the mouth over time. J Evid Based Dent Pract, 2010, 10(1) : 21-22.
  • 3Sulkala M, Tervahartiala T, Sorsa T, et al. Matrix metalloproteinase-8 (MMP-8) is the major collagenase in human dentin. Arch Oral Biol, 2007, 52(2) : 121-127.
  • 4Mazzoni A, Pashley DH, Nishitani Y, et al. Reactivation of inactivated endogenous proteolytic activities in phosphoric acid-etched dentine by etch-and-rinse adhesives. Biomaterials, 2006, 27 (25) : 4470-4476.
  • 5Pashley DH, Tay FR, Yiu C, et al. Collagen degradation by host-derived enzymes during aging. J Dent Res, 2004, 83 ( 3 ) : 216-221.
  • 6Gendron R, Grenier D, Sorsa T, et al. Inhibition of the activities of matrix metalloproteinases 2, 8, and 9 by chlorhexidine. Clin Diagn Lab Immunol, 1999, 6(3) : 437-439.
  • 7Osorio R, Yamauti M, Osorio E, et al. Effect of dentin etching and chlorhexidine application on metalloproteinase-mediated collagen degradation. Eur J Oral Sci, 2011, 119( 1 ) : 79-85.
  • 8Sadek FT, Braga RR, Muench A, et al. Ethanol wet-bonding challenges current anti-degradation strategy. J Dent Res, 2010,89(12) : 1499-1504.
  • 9Huang L, Xiao YH, Xing XD, et al. Antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers on oral pathogens. Arch Oral Biol, 2011,56(4) : 367-373.
  • 10Tezvergil-Mutluay A, Agee KA, Uchiyama T, et al. The inhibitory effects of quaternary ammonium methacrylates on soluble and matrix-bound MMPs. J Dent Res, 2011, 90(4) : 535-540.

共引文献10

同被引文献46

引证文献4

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部