Whitford G M, Pashley D H
Calcif Tissue Int. 1984 May;36(3):302-7. doi: 10.1007/BF02405334.
The influence of gastric acidity on the absorption of intragastrically administered fluoride was investigated in rats. Intact animals were pretreated with atropine or cimetidine to reduce gastric acid secretion or were given fluoride in NaHCO3 to reduce the acidity of the gastric contents. Compared with pentagastrin-treated animals or animals that received fluoride in 0.1 N HCl, their rate of fluoride absorption was markedly reduced as judged by lower plasma fluoride concentrations and areas under the time-plasma concentration curves, especially during the first hour after dosing. In crossover studies with the stomachs isolated in situ, fluoride absorption was at least 50% faster from a pH 2.1 buffer compared with its absorption from a pH 7.1 buffer. The findings are consistent with the hypothesis that fluoride is absorbed from the gastric lumen principally as the undissociated molecule, HF. The results may contribute to a more complete understanding of acute fluoride toxicity, the development of dental fluorosis and, perhaps, the use of fluoride in the treatment of osteoporosis.
在大鼠中研究了胃酸度对胃内给予氟化物吸收的影响。对完整动物用阿托品或西咪替丁预处理以减少胃酸分泌,或给予碳酸氢钠中的氟化物以降低胃内容物的酸度。与五肽胃泌素处理的动物或在0.1N盐酸中接受氟化物的动物相比,根据较低的血浆氟化物浓度和血浆浓度-时间曲线下面积判断,它们的氟吸收速率明显降低,尤其是在给药后的第一小时。在原位分离胃的交叉研究中,与从pH 7.1缓冲液中吸收相比,氟化物从pH 2.1缓冲液中的吸收至少快50%。这些发现与氟化物主要以未解离分子HF从胃腔吸收的假设一致。这些结果可能有助于更全面地理解急性氟中毒、氟斑牙的发生,或许还有氟化物在骨质疏松症治疗中的应用。