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大鼠胃肠道对二氟磷酸钠和一氟磷酸钙中氟化物的吸收

Fluoride absorption from disodium and calcium monofluorophosphates from the gastrointestinal tract of rats.

作者信息

Villa A, Rosenkranz C, Garrido A

机构信息

Unidad de Bioquimica Farmacologica y Lipidos. INTA, Universidad de Chile; Santiago.

出版信息

Res Commun Chem Pathol Pharmacol. 1993 Jul;81(1):53-67.

PMID:8210690
Abstract

The contribution of the stomach and the small intestine to the in vivo absorption of fluoride from disodium and calcium monofluorophosphates was studied in comparison with that observed when sodium fluoride is given to rats. In vitro experiments with ligated duodena were also carried out. Fasted rats were given orally 50 micrograms of fluoride in pH 6.3 buffered disodium monofluorophosphate solutions with and without 50 mM added calcium. The same amount of fluoride was administered in the form of an aqueous sodium fluoride solution. In both cases the fluoride solutions contained trace amounts of (14C)-labeled polyethyleneglycol as a marker for the study of water movement through the gastrointestinal tract. Results obtained show the small intestine as the main site of the absorption of the studied compounds. Under the fasting conditions employed in our study gastric absorption was in turn, almost negligible. While fluoride transport from sodium fluoride seems to occur through a difussion mechanism, disodium and calcium monofluorophosphates appear to be absorbed through a more complex mechanism involving an enzymatic hydrolysis and an independent and possibly parallel direct tissue absorption of a soluble, neutral calcium monofluorophosphate complex.

摘要

与给大鼠服用氟化钠时的情况相比,研究了胃和小肠对二氟磷酸钠和一氟磷酸钙在体内吸收氟的贡献。还进行了结扎十二指肠的体外实验。给禁食的大鼠口服50微克氟,其存在于pH 6.3的缓冲二氟磷酸钠溶液中,添加和不添加50 mM钙。以氟化钠水溶液的形式给予相同量的氟。在这两种情况下,氟溶液都含有痕量的(14C)标记聚乙二醇作为研究水通过胃肠道运动的标志物。获得的结果表明小肠是所研究化合物吸收的主要部位。在我们研究采用的禁食条件下,胃的吸收几乎可以忽略不计。虽然氟化钠的氟转运似乎通过扩散机制发生,但二氟磷酸钠和一氟磷酸钙似乎通过更复杂的机制被吸收,该机制涉及酶促水解以及可溶性中性一氟磷酸钙络合物的独立且可能平行的直接组织吸收。

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