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碱生成可被视为龋病控制的一种方法吗?

Could alkali production be considered an approach for caries control?

机构信息

Department of Operative Dentistry, College of Dentistry, University of Florida, Gainesville, FL 32610-04415, USA.

出版信息

Caries Res. 2010;44(6):547-54. doi: 10.1159/000321139. Epub 2010 Nov 13.

Abstract

This study investigated the relationship of arginine deiminase (ADS) and urease activities with dental caries through a case-control study. ADS and urease activities were measured in dental smooth-surface supragingival plaque and whole saliva samples from 93 subjects, who were in three different groups: caries-free (n = 31), caries-active (n = 30), and caries-experienced (n = 32). ADS activity was measured by quantification of the ammonia generated from the incubation of plaque and saliva samples in a mixture containing 50 mM arginine-HCl and 50 mM Tris-maleate buffer, pH 6.0. ADS-specific activity was defined as nanomoles of ammonia generated per minute per milligram of protein. Urease activity was determined by quantification of ammonia produced from 50 mM urea. For bacterial identification and enumeration real-time qPCR analysis was used. Groups were compared using Kruskal-Wallis tests. Spearman correlations were used to analyze plaque metabolic activity and bacterial relationships. The results revealed significantly higher ammonia production from arginine in saliva (1.06 vs. 0.18; p < 0.0001) and plaque samples (1.74 vs. 0.58; p < 0.0001) from caries-free subjects compared to caries-active subjects. Urease levels were about 3-fold higher in the plaque of caries-free subjects (p < 0.0001). Although higher urease activity in saliva of caries-experienced and caries-free subjects was evident, no significant difference was found between the groups.

摘要

本研究通过病例对照研究调查了精氨酸脱亚氨酶(ADS)和脲酶活性与龋齿的关系。在三个不同组的 93 名受试者中测量了牙面光滑表面龈上菌斑和全唾液样本中的 ADS 和脲酶活性,这些受试者分别为:无龋(n = 31)、活跃性龋(n = 30)和经历性龋(n = 32)。通过在含有 50mM 精氨酸-HCl 和 50mM 三羟甲基氨基甲烷-马来酸缓冲液(pH 6.0)的混合物中孵育菌斑和唾液样本,定量生成的氨来测量 ADS 活性。将 ADS 比活性定义为每分钟每毫克蛋白质生成的氨的毫摩尔数。脲酶活性通过定量 50mM 尿素产生的氨来确定。使用实时 qPCR 分析进行细菌鉴定和计数。使用 Kruskal-Wallis 检验比较组间差异。使用 Spearman 相关性分析来分析菌斑代谢活性和细菌之间的关系。结果表明,与活跃性龋组相比,无龋组唾液(1.06 比 0.18;p < 0.0001)和菌斑样本(1.74 比 0.58;p < 0.0001)中从精氨酸生成的氨明显更高。无龋组菌斑中的脲酶水平约高 3 倍(p < 0.0001)。尽管在经历性龋和无龋组的唾液中观察到更高的脲酶活性,但组间无显著差异。

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