了解气体递质在慢性全身性牙周炎发病过程中的作用的新方法

A. V. Leonteva, A. Blinova, Y. Chervinets, V. A. Rumyantsev, V. Chervinets
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The control group included 33 patients aged 27 to 55 without periodontal disease. The samples from the back of the tongue were the study material. The gas chromatography determined the production of gas signaling molecules using the Khromatek-crystal 5000.2 device. The measurement of the amount of released gases was in % (for O2, N2) and ppm (0.001 mg/mL) for other gas molecules (CO2, CH4, NO, CO, H2S).Results. The metabolic activity of streptococci only for the production of NO (p = 0.002) and CO (p = 0.008) appeared to have a statistically significant difference. In periodontal inflammation, there was practically no NO emission by Streptococci spp., and the concentration of CO was ten times higher than in the group of healthy individuals. The difference in the number of other signaling gas molecules was not statistically significant (p > 0.05) in healthy people and patients with chronic generalized periodontitis. 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引用次数: 0

摘要

相关性。最近对微生物气体物质(O2、N2、CO2、CH4、NO、CO、H2S)作用的研究表明,它们不仅能调节宿主的新陈代谢活动及其神经系统的功能,特别是还能参与某些疾病的发病机制。然而,国内外文献中关于口腔微生物群(链球菌属和葡萄球菌属)产生气体信号分子以及慢性炎症性牙周病发展过程中气体成分变化的数据很少。研究包括 69 人。主组包括 36 名经临床证实患有中度慢性全身性牙周炎的患者,年龄在 35 至 67 岁之间。对照组包括 33 名无牙周病的患者,年龄在 27 至 55 岁之间。研究材料为舌背样本。气相色谱法使用 Khromatek-crystal 5000.2 设备测定气体信号分子的产生。气体释放量的测量单位是%(O2、N2),其他气体分子(CO2、CH4、NO、CO、H2S)的测量单位是ppm(0.001 mg/mL)。链球菌的新陈代谢活动仅在产生 NO(p = 0.002)和 CO(p = 0.008)方面有显著的统计学差异。在牙周炎症中,链球菌几乎不释放 NO,而 CO 的浓度是健康人的十倍。健康人和慢性全身性牙周炎患者在其他信号气体分子数量上的差异没有统计学意义(P > 0.05)。在葡萄球菌属气体递质的产生中,N2 的产生(p = 0.007,在对比组中增加)在统计学上有显著差异。与链球菌取样一样,牙周炎患者的 CO 量也明显增加。某些种类的葡萄球菌在主要组中整个气体分子范围的产生量都有明显下降。同时,与链球菌属不同,葡萄球菌属在慢性牙周炎中吸收的一氧化氮量要高得多。在慢性全身性牙周炎和炎症患者中,口腔微生物群的活性较差,产生的气体递质浓度较低,因此无法参与炎症过程的消退,从而导致疾病的恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new approach to understanding the role of gasotransmitters in the development of chronic generalized periodontitis
Relevance. Recent studies investigating the role of the microbial gaseous substances (O2, N2, CO2, CH4, NO, CO, H2S) indicate not only in the regulation of the host's metabolic activity and the functioning of its nervous system, in particular but also their participation the pathogenesis of some diseases. However, there is scarce data in the national and international literature on the production of gas signaling molecules by the oral microbiota (Streptococcus spp. and Staphylococcus spp.) and the changes in the gas composition during the development of chronic inflammatory periodontal diseases.Material and methods. The study included 69 people. The main group included 36 patients aged 35 to 67 years with clinically confirmed moderate chronic generalized periodontitis. The control group included 33 patients aged 27 to 55 without periodontal disease. The samples from the back of the tongue were the study material. The gas chromatography determined the production of gas signaling molecules using the Khromatek-crystal 5000.2 device. The measurement of the amount of released gases was in % (for O2, N2) and ppm (0.001 mg/mL) for other gas molecules (CO2, CH4, NO, CO, H2S).Results. The metabolic activity of streptococci only for the production of NO (p = 0.002) and CO (p = 0.008) appeared to have a statistically significant difference. In periodontal inflammation, there was practically no NO emission by Streptococci spp., and the concentration of CO was ten times higher than in the group of healthy individuals. The difference in the number of other signaling gas molecules was not statistically significant (p > 0.05) in healthy people and patients with chronic generalized periodontitis. In the production of gasotransmitters among Staphylococcus spp., N2 production (p = 0.007, increasing in the comparison group) was statistically significantly different. As in the streptococcal sampling, the amount of CO significantly increased in periodontal inflammation. Certain species of staphylococci showed a significant decrease in the production of the entire gas molecule range in the main group. At the same time, unlike Streptococcus spp., Staphylococcus spp. absorbed a much higher amount of nitric oxide in chronic periodontitis.Conclusion. In patients with chronic generalized periodontitis and inflammation, the oral microbiota is poorly active and produces a low concentration of gasotransmitters, so they cannot participate in inflammatory process reduction, thereby contributing to the progression of the disease.
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