Department of Pediatric Dentistry, School of Dentistry, University of North Carolina at Chapel Hill, 228 Brauer Hall, CB# 7450, Chapel Hill, NC 27599, USA.
J Dent Res. 2011 May;90(5):552-60. doi: 10.1177/0022034510384626. Epub 2010 Oct 6.
Fluorides are present in the environment. Excessive systemic exposure to fluorides can lead to disturbances of bone homeostasis (skeletal fluorosis) and enamel development (dental/enamel fluorosis). The severity of dental fluorosis is also dependent upon fluoride dose and the timing and duration of fluoride exposure. Fluoride's actions on bone cells predominate as anabolic effects both in vitro and in vivo. More recently, fluoride has been shown to induce osteoclastogenesis in mice. Fluorides appear to mediate their actions through the MAPK signaling pathway and can lead to changes in gene expression, cell stress, and cell death. Different strains of inbred mice demonstrate differential physiological responses to ingested fluoride. Genetic studies in mice are capable of identifying and characterizing fluoride-responsive genetic variations. Ultimately, this can lead to the identification of at-risk human populations who are susceptible to the unwanted or potentially adverse effects of fluoride action and to the elucidation of fundamental mechanisms by which fluoride affects biomineralization.
氟化物存在于环境中。过量的系统性氟化物暴露会导致骨稳态(骨骼氟中毒)和牙釉质发育(牙齿/牙釉质氟中毒)紊乱。氟中毒的严重程度还取决于氟化物剂量以及氟化物暴露的时间和持续时间。氟化物对骨细胞的作用主要表现为体外和体内的合成代谢作用。最近,研究表明氟化物可以诱导小鼠破骨细胞形成。氟化物似乎通过 MAPK 信号通路发挥其作用,并可能导致基因表达、细胞应激和细胞死亡的变化。不同品系的近交系小鼠对摄入的氟化物表现出不同的生理反应。小鼠的遗传研究能够识别和描述对氟化物有反应的遗传变异。最终,这可以确定易受氟化物作用的不良或潜在不良影响的高危人群,并阐明氟化物影响生物矿化的基本机制。