Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Al. Octávio Pinheiro Brisolla, 9-75, 17012-901, Bauru, São Paulo, Brazil.
Department of Technology and Science, University of Sagrado Coração, Bauru, SP, Brazil.
Chemosphere. 2019 Dec;236:124357. doi: 10.1016/j.chemosphere.2019.124357. Epub 2019 Jul 12.
The mechanisms involved in changes in energy metabolism caused by excessive exposure to fluoride (F) are not completely understood. The present study employed proteomic tools to investigate the molecular mechanisms underlying the dose- and time-dependency of the effects of F in the rat liver mitochondria. Thirty-six male Wistar rats received water containing 0, 15 or 50 mgF/L (as NaF) for 20 or 60 days. Rat liver mitochondria were isolated and the proteome profiles were examined using label-free quantitative nLC-MS/MS. PLGS software was used to detect changes in protein expression among the different groups. The bioinformatics analysis was done using the software CYTOSCAPE 3.0.7 (Java) with the aid of ClueGo plugin. The dose of 15 mgF/L, when administered for 20 days, reduced glycolysis, which was counterbalanced by an increase in other energetic pathways. At 60 days, however, an increase in all energy pathways was observed. On the other hand, the dose of 50 mgF/L, when administered for 20 days, reduced the enzymes involved in all energetic pathways, indicating a lower rate of energy production, with less generation of ROS and consequent reduction of antioxidant enzymes. However, when the 50 mgF/L dose was administered for 60 days, an increase in energy metabolism was seen but in general no changes were observed in the antioxidant enzymes. Except for the group treated with 50 mgF/L for 20 days, all the other groups had alterations in proteins in attempt to maintain calcium homeostasis and avoid apoptosis. The results suggest that the organism seems to adapt to the effects of F over time, activating pathways to reduce the toxicity of this ion. Ultimately, our findings corroborate the safety of the use of fluoride for caries control.
氟化物(F)暴露过度引起的能量代谢变化的机制尚不完全清楚。本研究采用蛋白质组学工具研究氟在大鼠肝线粒体中剂量和时间依赖性作用的分子机制。36 只雄性 Wistar 大鼠接受含有 0、15 或 50mgF/L(以 NaF 计)的水,为期 20 或 60 天。分离大鼠肝线粒体,使用无标记定量 nLC-MS/MS 检测不同组之间的蛋白质组谱。PLGS 软件用于检测不同组之间蛋白质表达的变化。使用 CYTOSCAPE 3.0.7(Java)软件并借助 ClueGo 插件进行生物信息学分析。当剂量为 15mgF/L 且处理 20 天时,会降低糖酵解,这被其他能量途径的增加所抵消。然而,60 天时,观察到所有能量途径的增加。另一方面,当剂量为 50mgF/L 且处理 20 天时,会降低所有能量途径的酶,表明能量产生率降低,产生的 ROS 减少,抗氧化酶随之减少。然而,当 50mgF/L 剂量处理 60 天时,会观察到能量代谢增加,但一般来说,抗氧化酶没有变化。除了用 50mgF/L 处理 20 天的组外,所有其他组的蛋白质都发生了变化,试图维持钙稳态并避免细胞凋亡。结果表明,随着时间的推移,机体似乎适应了 F 的影响,激活了减少这种离子毒性的途径。最终,我们的发现证实了氟化物用于龋齿控制的安全性。