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Centre de Recherche en Nutrition Humaine dAuvergne, Unité Maladies Métaboliques et Micronutriments, INRA, Theix, 63122 St Genès Champanelle, France and * U.S. Department of Agriculture/ARS Childrens Nutrition Research Center, Baylor College of Medicine, Houston, TX 77030
1To whom correspondence should be addressed.
A sensitive and valid marker to assess magnesium (Mg) status in humans
is not available. The kinetically determined exchangeable pool masses
have been used for other minerals, such as zinc and selenium, as
markers of whole-body mineral status. To evaluate the validity of
this relationship for Mg, we measured the exchangeable pools of Mg in
rats over a range of magnesium dietary intakes. Rats weighing
170 g
were fed a control diet (500 mg Mg/kg), a marginally Mg-deficient
diet (200 mg/kg) or a severely Mg-deficient diet (60 mg Mg/kg) for
2 wk. Subsequently, rats were administered an intravenous injection of
25Mg, and the plasma 25Mg disappearance curve
was followed for the next 7 d. The following two methods were
employed to analyze the exchangeable pools of Mg: 1)
formal compartmental modeling and 2) a simplified
determination of the total mass of the rapidly exchangeable Mg pool
(EMgP). The mass of the three exchangeable pools (two extracellular
pools and one intracellular pool) determined by compartmental analysis
decreased in proportion to dietary Mg intake. EMgP, the combined pools
of Mg that exchange with the plasma Mg within 48 h, decreased
significantly as dietary Mg was lowered. It was positively correlated
with conventional markers of Mg status (total Mg in plasma, erythrocyte
and tibia Mg levels). Compartmental analysis assesses Mg exchangeable
pools more accurately, but determination of EMgP is simpler and faster.
Our findings demonstrate that the exchangeable pools of Mg constitute a
good marker of Mg status in rats.
KEY WORDS: magnesium exchangeable pool status rats
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