Trace Elements in Dental Enamel Can Be a Potential Factor of Advanced Tooth Wear

被引:3
作者
Zamojda, Elzbieta [1 ]
Orywal, Karolina [2 ]
Mroczko, Barbara [2 ]
Sierpinska, Teresa [1 ]
机构
[1] Med Univ Bialystok, Dept Prosthet Dent, 24 Sklodowskiej Curie Str, PL-15276 Bialystok, Poland
[2] Med Univ Bialystok, Dept Biochem Diagnost, 15A Waszyngtona Str, PL-15269 Bialystok, Poland
关键词
calcium; magnesium; zinc; copper; tooth wear; dentistry; MATRIX METALLOPROTEINASE-20; ZINC; COPPER; DEMINERALIZATION; HYDROXYAPATITE; CARIES;
D O I
10.3390/min13010125
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Enamel is the outermost layer of the tooth and has no ability to regenerate after tooth eruption. Its mineral composition is likely to be responsible for the enamel resistance to any agents that appear in oral cavity. The objective of this study was to compare the content of Ca, Mg, Zn and Cu in specific layers of healthy and worn tooth enamel. Three groups of dental enamel samples were analyzed. The amounts of Ca, Mg and Zn in the enamel bioptates were established using atomic absorption spectroscopy after an acid biopsy technique had been applied. The concentration of Cu was established using an electrothermic method with an AA spectrometer. The analysis was carried out using parametric tests (the Pearson's linear correlation coefficient and the t-test for the correlation coefficient). Results: A statistically significant difference was confirmed between the mean amount of zinc in severely worn dentition and all the layers in vitro and in vivo. Strong positive relationships between magnesium and zinc contents were shown at some depths. A significant difference was registered between the amount of copper in the severely worn dentitions compared to the superficial layer of the healthy teeth in vitro and in vivo. Conclusion: It appears that zinc metabolism may play an important role in enamel formation and may influence enamel's resistance to wear after tooth eruption.
引用
收藏
页数:9
相关论文
共 40 条
[1]   The effect of copper on demineralization of dental enamel [J].
Abdullah, A. Z. ;
Strafford, S. M. ;
Brookes, S. J. ;
Duggal, M. S. .
JOURNAL OF DENTAL RESEARCH, 2006, 85 (11) :1011-1015
[2]   Bioinformatic comparison of structures and homology-models of matrix metalloproteinases [J].
Andreini, C ;
Banci, L ;
Bertini, I ;
Luchinat, C ;
Rosato, A .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (01) :21-31
[3]  
[Anonymous], 2015, ISO/TS 11405, V3rd
[4]  
Aoba T, 1996, ANAT REC, V245, P208, DOI 10.1002/(SICI)1097-0185(199606)245:2<208::AID-AR8>3.0.CO
[5]  
2-S
[6]   DENTAL EROSION - A PRESENTING FEATURE OF GASTROESOPHAGEAL REFLUX DISEASE [J].
BARTLETT, DW ;
ANGGIANSAH, A ;
OWEN, W ;
EVANS, DF ;
SMITH, BGN .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1994, 6 (10) :895-900
[7]   A developmental comparison of matrix metalloproteinase-20 and amelogenin null mouse enamel [J].
Bartlett, John D. ;
Skobe, Ziedonis ;
Lee, Daniel H. ;
Wright, J. Timothy ;
Li, Yong ;
Kulkarni, Ashok B. ;
Gibson, Carolyn W. .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2006, 114 :18-23
[8]   Matrix metalloproteinase 20 promotes a smooth enamel surface, a strong dentino-enamel junction, and a decussating enamel rod pattern [J].
Bartlett, John D. ;
Skobe, Ziedonis ;
Nanci, Antonio ;
Smith, Charles E. .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2011, 119 :199-205
[9]  
Bialek M., 2014, Polish Journal of Public Health, V124, P160, DOI DOI 10.2478/PJPH-2014-0036
[10]   Copper ions inhibit the demineralisation of human enamel [J].
Brookes, SJ ;
Shore, RC ;
Robinson, C ;
Wood, SR ;
Kirkham, J .
ARCHIVES OF ORAL BIOLOGY, 2003, 48 (01) :25-30