Arthur Rodrigo Alex, Kohara Eduardo Kazuo, Waeiss Robert Aaron, Eckert George J, Zero Domenick, Ando Masatoshi
Faculty of Dentistry, Federal University of Rio Grande do Sul, Rua Ramiro Barcelos 2492, 90035-003 Porto Alegre, RS, Brazil.
Oral Health Research Institute, Indiana School of Dentistry, 415 Lansing Street, Indianapolis, IN 46202, USA.
J Oral Dis. 2014;2014. doi: 10.1155/2014/348032.
The aim of this study was to evaluate both sucrose and fluoride concentrations and time of biofilm formation on enamel carious lesions induced by an artificial-mouth caries model. For Study 1, biofilms formed by streptococci and lactobacilli were grown on the surface of human enamel slabs and exposed to artificial saliva containing 0.50 or 0.75 ppmF (22.5 h/d) and broth containing 3 or 5% sucrose (30 min; 3x/d) over 5 d. In Study 2, biofilms were grown in the presence of 0.75 ppmF and 3% sucrose over 3 and 9 days. Counts of viable cells on biofilms, lesion depth (LD), and the integrated mineral loss (IML) on enamel specimens were assessed at the end of the tested conditions. Counts of total viable cells and were affected by sucrose and fluoride concentrations as well as by time of biofilm formation. Enamel carious lesions were shallower and IML was lower in the presence of 0.75 ppmF than in the presence of 0.50 ppmF ( < 0.005). No significant effect of sucrose concentrations was found with respect to LD and IML ( > 0.25). Additionally, deeper lesions and higher IML were found after 9 d of biofilm formation ( < 0.005). Distinct sucrose concentrations did not affect enamel carious lesion development. The severity of enamel demineralization was reduced by the presence of the higher fluoride concentration. Additionally, an increase in the time of biofilm formation produced greater demineralization. Our results also suggest that the present model is suitable for studying aspects related to caries lesion development.
本研究的目的是评估人工口腔龋模型诱导的牙釉质龋损上生物膜形成时的蔗糖和氟化物浓度以及时间。在研究1中,由链球菌和乳酸菌形成的生物膜在人牙釉质块表面生长,并在5天内暴露于含0.50或0.75 ppmF(每天22.5小时)的人工唾液和含3%或5%蔗糖的肉汤(30分钟;每天3次)中。在研究2中,生物膜在含0.75 ppmF和3%蔗糖的条件下生长3天和9天。在测试条件结束时,评估生物膜上的活菌计数、龋损深度(LD)和牙釉质标本上的矿物质损失总量(IML)。总活菌计数受蔗糖和氟化物浓度以及生物膜形成时间的影响。与存在0.50 ppmF相比,存在0.75 ppmF时牙釉质龋损更浅,IML更低(P<0.005)。未发现蔗糖浓度对LD和IML有显著影响(P>0.25)。此外,生物膜形成9天后发现龋损更深,IML更高(P<0.005)。不同的蔗糖浓度不影响牙釉质龋损的发展。较高氟化物浓度的存在降低了牙釉质脱矿的严重程度。此外,生物膜形成时间的增加导致更大程度的脱矿。我们的结果还表明,当前模型适用于研究与龋损发展相关的方面。