Sabatier, Magalie, Fré dé ric Pont, Maurice J. Arnaud, and Judith R. Turnlund. A compartmental model of magnesium metabolism in healthy men based on two stable isotope tracers. Am J Physiol Regul Integr Comp Physiol 285: R656-R663, 2003. First published May 29, 2003 10.1152/ ajpregu.00749.2002The aim of this study was to build a compartmental model of magnesium (Mg) kinetics by using data collected from six healthy adult men after oral administration of 26 Mg and intravenous administration of 25 Mg. Blood, urine, and feces were collected for 12 days after administration of the isotopes. Isotopic ratios were determined by inductively coupled plasma-mass spectrometry. Data were analyzed for each subject using SAAMII. We began with a compartmental model previously proposed (Avioli LV and Berman M. J Appl Physiol 21: 1688-1694) and developed an alternative approach to resolve the discrepancy between model-predicted curves and experimental data. This analysis enables the exploration of 25% of total body Mg that exchanges rapidly from plasma compartment with two extraplasma pools. One of the extraplasma compartments contains 80% of the exchangeable Mg with a transport rate of 48 Ϯ 13 mg/h. The second exchanges 179 Ϯ 88 mg of Mg/h. The model permitted estimation of kinetic parameters as well as fractional Mg absorption and fecal endogenous excretion. magnesium absorption; magnesium fecal endogenous excretion; inductively coupled plasma-mass spectrometry MAGNESIUM (Mg) is an essential mineral for humans, with a recommended dietary allowance (RDA) of 420 mg/day for adult men (17a). Its physiological role is mainly related to enzyme activity (27), and Mg deficiency has been associated with several pathologies. Despite its importance, minimal information is available regarding the distribution and turnover of exchangeable Mg in humans. The lack of studies of Mg metabolism is due primarily to limitations of the tracers that can be used. The Mg radioisotope has a short half-life (21.8 h), and the precise measurement of the enrichment of relatively abundant stable isotopes presented a challenge until the 1990s for nutrition research. This is accentuated by the fact that few tissues are available for analysis in humans in contrast to animals. These limitations can be overcome in part with compartmental analysis of Mg tracer kinetics, which can be used to obtain quantitative or predictive information about the dynamics of a system. This mathematical description of mineral distribution provides valuable insight into the metabolism of many nutrients in humans (41). Compartmental models have been developed for several essential minerals on the basis of stable isotope studies in humans, including calcium (37, 42, 43), zinc (13, 21, 31, 38 and 39), copper (6, 30), and molybdenum (16,33,34). In addition, parameters deduced from the model can be used as markers of trace element nutritional status. It has been demonstrated for selenium (8,19) and Zn (17) that, depending on the ingested amount of a mineral, pool size could vary and ...